Thursday, June 12, 2014

Dandy Walker Syndrome

Dandy Walker Syndrome
Dandy walker syndrome occurs when there are defects on some parts of the brain, particularly the cerebellum and surrounding areas. This condition causes a wide array of problems that can either be inconspicuous or obvious. People affected by this syndrome have difficulties in controlling their movements; coordination of the eyes and muscles; speaking and understanding language. They tend to have defective organs, such as the kidneys, urinary tract and heart, to name a few.










Dandy walker syndrome is present at birth and early diagnosis can significantly improve the chances of survival and normal functioning. This differs from patient to patient, though, as each case is unique and life expectancy is cut short for those who are born with several defects or those individuals suffering from health problems.


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  • 3 Occurrence of Dandy Walker Syndrome
  • 4 Treatment of Dandy Walker Syndrome
  • 5 Dandy Walker Syndrome Pictures

  • Causes of Dandy Walker Syndrome


    Dandy Walker syndrome (DWS) is brought about by an abnormal brain development that caused the cerebellum to become defective or abnormally formed, specifically at the posterior part of the brain. In many of DWS cases, some other parts of the cerebellum are defective as well. The abnormalities observed in the cerebellum that lead to the syndrome involve the following:



    • Very small or completely absent cerebellar vermis.  This is a worm-shaped tube that connects the two sides of the cerebellum.



    • Abnormally large posterior fossa or the small part of the skull that houses the cerebellum and brainstem, due to the presence of cyst.



    • Development of cyst in the fluid-filled cavity called fourth ventricle through which fluid coming from the brain passes as it goes to the spinal column.


    The exact cause of the syndrome is still unknown. However, extensive research has revealed sufficient information that has helped in the understanding of the nature of the condition.



    • Genetic mutations


    Mutations in some of the genes of the individuals afflicted with DWS had been observed.



    • Chromosomal abnormalities


    Studies showed that those with DWS have extra copies of some chromosomes, particularly chromosomes 18, 13, 21 or 9. Moreover, the condition has been found to also occur in people born with one extra copy of all chromosomes in every cell.


    Symptoms of Dandy Walker Syndrome


    The cerebellum or the area of the brain that is involved in movement control, coordination and cognition is the defective part in the case of DWS. Persons affected by DWS will have problems in relation to these neurological functions but at varying degrees. These problems may go unnoticed for some people or be very obvious in others.


    Among the problems caused by DWS to include:




    • Delayed motor development


    Babies affected by this syndrome learn to crawl, walk or perform coordinated movements much later than normal babies of their age.




    • Problems with coordination and movement


    There is lack of coordination between muscles resulting in muscle stiffness, unsteadiness, and jerky eye movements. Those afflicted by the condition also seem to be irritable and deal with seizures frequently. Vision and hearing are affected as well.












    • Cognitive defects


    Sufferers experience some measure of intellectual disability which could be mild or severe. These cognitive deficits make it difficult to learn how to speak and understand language.




    • External and internal malformations


    A DWS child has a progressively enlarged skull, causing bigger head circumference. There might likewise be some bulge at the back of the skull. The vast majority of DWS patients have some form of heart defect, abnormal facial appearance, extra fingers or toes, and malformed kidneys or urogenital tract.


    Around 80% of DWS cases are detected during the first 12 months of life. Some develop the symptoms later during childhood.


    Occurrence of Dandy Walker Syndrome


    Statistics show that DWS rarely occurs, affecting approximately 1 child out of 25,000 to 30,000 births. It mostly occurs as a result of random events during the early stages of pregnancy. There are no known risk factors for the syndrome but experts believe that certain things can affect the optimum brain development during pregnancy, hence, resulting in DWS. These include:



    • Rubella infections

    • Toxoplasmosis

    • Exposure to teratogens

    • Diabetes


    Some children inherit the defective gene that causes some of the features of Dander walker syndrome. However, relevant environmental factors should also be present for this to happen.


    Treatment of Dandy Walker Syndrome


    The treatment for the condition aims to provide some measure of relief by addressing the problems associated with it as well as prevent them from aggravating. For instance, there is a swelling on the back part of the skull due to fluid buildup thus causing intracranial pressure. This is dealt with by draining the fluid through inserting a tube into the skull. The intracranial pressure felt will then be reduced. Other accompanying problems are treated as well, including multiple malformations and organ defects. Meanwhile, specialized education can provide the needed support for intellectual or learning disabilities; speech therapy can help the patient speak and understand speech. A patient affected by Dandy Walker syndrome will also benefit from physiotherapy and occupational therapy.


    Dandy Walker Syndrome Pictures
















    Down Syndrome – Pictures, Life Expectancy, Causes, Symptoms,Treatment

    Down Syndrome – Pictures, Life Expectancy, Causes, Symptoms,Treatment
    Down syndrome is a genetic disorder, caused due to abnormality in the cell division involving chromosome 21. The disorder causes a permanent developmental delay, mental retardation and many other problems. The severities of Down syndrome vary and as such the problems of developmental delays also vary from mild to serious conditions. Learning difficulties are the common disability in Down syndrome.










    When one of the three types of abnormal cell division involving chromosome 21 occur, Down syndrome is caused. The extra genetic material from chromosome 21, which is responsible for vital characteristic features of developmental difficulties are caused by all the three cell division abnormalities.


    Early intervention and a better understanding of this disorder can help the children and adults affected by this syndrome.


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    Symptoms of Down syndrome


    The following are some of the signs and symptoms of Down syndrome:



    • Different and distinct facial features

    • A little/tiny head

    • Short neck

    • Flat face

    • Unusually upward slanting eyes that are different from the ethnic features.

    • Ears with a peculiar shape

    • A protruding tongue


    Children with this disorder may also have the following additional signs:



    • Short, but broad hands along with a single crease in palm

    • Excessive flexibility

    • Poor muscle tone

    • Comparatively short fingers


    Down syndrome affected children suffer from slow growth and are shorter in height. In comparison to other children, the Down syndrome affected children take double the time for growth and achieving developmental milestones such as crawling and sitting. They also elicit moderate mental retardation.


    Children born with Down syndrome develop various complications as they grow. They are:



    • Leukemia

    • Obesity

    • Risk of dementia is more prevalent at an age of more than 40 along with higher rate of seizures.

    • Risk of infectious diseases due to weak immune system often causing pneumonia.

    • Heart disordersthat need surgery

    • Sleep apnea

    • Other problems like thyroid disorder, early menopause, gastrointestinal blockage, hearing loss, poor vision, skeletal disorder, seizures, and premature aging.


    Causes of Down syndrome


    Generally, each cell of human being contains 23 pairs of chromosomes. The children get one chromosome of eachpair from their father and as well from their mother. The syndrome occurs when one of the three abnormal cell division connected to chromosome 21occurs. The cell division abnormalities result in additional genetic materialin chromosome 21 which is responsible for thedistinctive characteristics and developmental anomalies associated with the condition


    The following are the three genetic variations that cause Down syndrome:











    • Mosaic Down syndrome:It is a rare form of syndrome that occurs whenever the children possess some cells with an extra copy of chromosome 21. The combination of normal cells with abnormal cells cause abnormal cell division after fertilization.

    • Trisomy 21:An infant with trisomy 21 possess three copies of chromosome 21, instead of two usual copies in all of his/her cells. This anomaly is caused due to abnormal cell division at the time of sperm cell or egg cell development. More than 90% of Down syndrome cases are caused by this trisomy 21.

    • Translocation Down syndrome:Whenever a part of the chromosome 21 remains attached to another chromosome (Translocated) at the time of conception or earlier, then it can cause Down syndrome. Children with translocation syndrome have additional material from the attached chromosome 21 in addition to the usual two copies of chromosome 21.The responsible factors for this syndrome are unknown.


    Down syndrome is not inherited, but caused due to mistakes in cell division during the developmental stage of sperm or egg, or duringconception;except the translocation Down syndrome which may be passed on to the child from parent. Only 4% of the children are affected by translocation Down syndrome and only just half of them have inherited it from parents. The presence of some rearranged genetic material, even without extra genetic material, can also cause translocation Down syndrome. The chance of passing the translocation syndrome is 3% from father and 10 to 15% from mother.


    An increased maternal age also increases the risk to conceiving a child with Down syndrome. The possibility expands along with the age. For example, the risk of conceiving a child with Down syndrome at the age of 35 is 1 in 400; while it is 1 in 35 at the age of 45.


    Treatment of Down syndrome


    With the medical facility and treatment advancements, the average life expectancy of people with Down syndrome has increased up to 50 years.


    Early intervention programs for children with Down syndrome will improve their abilities and their quality of life. The following are some of the treatments for Down syndrome affected children:



    • Administering of medicines as per the demands of the condition.

    • Early stimulation with appropriate sensory, motor, and other activitiesthat promote self-help.

    • Depending on the type of disorder, specialists from various fields will provide the needed treatments.

    • Self preparation to face the difficulties that may come while taking care of the affected child.

    • Consulting a genetic counselor before conceiving, if you are in the increased risk group

    • Seeking help from support groups


    Down Syndrome life expectancy


    People with Down syndrome have shorter than average life expectancy. However improvements in medical care and ongoing research have made it possible for people to have a longer life span. Back in 1912, the average life expectancy for Down Syndrome was 12 years; now it has increased to 60 years. It has been observed that most people who live up to their 40s and 50s, tend to get affected from neurodegenerative diseases like Alzheimer’s.


    Down Syndrome Pictures
















    Stevens-Johnson Syndrome

    Stevens-Johnson Syndrome
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    What is Stevens-Johnson Syndrome?


    It is a severe and rare condition wherein the mucous membranes and the skin have a serious reaction to infection or a certain drug. On most occasions, the disorder starts with flu-like signs which are then followed by the appearance of a painful, purplish or red rash that spreads and causes blisters. This will eventually result in the uppermost layer of the skin to die and fall off.










    Stevens-Johnson syndrome is considered as a medical emergency that generally involves hospitalization. The aim of the treatment is to eradicate the existing cause, control the symptoms and minimize the complications.


    The recovery period of Stevens-Johnson syndrome can last from a few weeks to many months and usually depends on the severity of the condition. In case, a certain drug was diagnosed as the underlying cause of the condition, then the affected individual has to stop the intake of that medication and others like it.


    Stevens-Johnson Syndrome Symptoms


    Some of the symptoms of Stevens-Johnson syndrome are listed below:



    • Swelling of the face

    • Hives

    • Swelling of the tongue

    • The skin may be painful

    • The skin and mucous membranes, particularly the nose, mouth and eyes may experience blisters

    • A purplish or reddish rash that tends to spread within a few hours or days

    • The skin may slough off or shed


    Individuals affected by Stevens-Johnson syndrome may experience the below mentioned symptoms, many days prior to the appearance of the rash:



    • The eyes may experience burning sensations

    • Increased soreness of the throat

    • Cough

    • Fever


    Some of the possible complications that may result due to Stevens-Johnson syndrome are discussed below:



    • The acute infection that affects the skin may result in secondary skin infections such as cellulitis, meningitis, etc. which can be life threatening. Meningitis is an infection of the membranes and fluid that surround the spinal cord and the brain.

    • The rash that results due to Stevens-Johnson syndrome can lead to many eye problems like eye inflammation. Mild cases of the condition may lead to dry eyes and irritation. Severe cases of the disorder can result in extreme tissue damage as well as scarring inside the eyes which can eventually lead to blindness

    • One of the worst complications of Stevens-Johnson syndrome is sepsis wherein bacteria tends to enter the body via an infection site and spreads to all the parts of the body through the bloodstream. Sepsis tends to spread rapidly and can result in organ failure, shock and even death.

    • There may be permanent damage of the skin. Once Stevens-Johnson syndrome is treated and the skin grows back, it may develop pigmentation and irregular bumps. There may be scarring of the skin. The hair may not grow back or fall out. Also, the toenails and fingernails may grow abnormally

    • Stevens-Johnson syndrome can also result in damage of the internal organs as well as formation of lesions in them. This can lead to inflammation of the heart, liver, lungs and kidneys.


    Causes of Stevens-Johnson syndrome


    The definite cause of Stevens-Johnson syndrome cannot be always determined. In most cases, the disorder is caused due to an allergic reaction to an infection, a medication or an illness.


    Medications are the primary cause of Stevens-Johnson syndrome. Some of drugs that are known to cause the condition are as follows:











    • Allopurinol and other anti-gout drugs

    • Different types of penicillin that are consumed to cure infections

    • Nonsteroidal anti-inflammatory drugs or NSAIDs that are used to alleviate pain

    • Anticonvulsants that are used to manage seizure disorders


    Some infectious causes of Stevens-Johnson syndrome include the following:



    • Herpes zoster or Herpes simplex

    • Typhoid

    • HIV

    • Influenza

    • Diphtheria

    • Hepatitis


    In certain cases, the condition may be caused as a response or reaction to physical stimuli such as ultraviolet light or radiation therapy


    Some of the risk factors that increased the vulnerability to developing Stevens-Johnson syndrome include the following:



    • Individuals who have a gene known as HLA-B12 are at greater risk to the condition

    • Presence of conditions such as lupus, HIV and other disorders that impair the immune system


    Stevens-Johnson Syndrome Treatment


    The treatment of Stevens-Johnson syndrome involves hospitalization of the affected individual, often in the burn unit or the ICU



    • The first step of the treatment is to stop the intake of all medications. It is not possible to identify the exact medication that has caused the condition, hence the consumption of all medications.


    While at the hospital, the Stevens-Johnson syndrome patient may get the following supportive care:



    • The use of wet, cool compresses to soothe the wounds while they heal

    • Removal of the dead skin and dressing the wounds with a topical anesthetic

    • Stevens-Johnson syndrome can result in sever loss of fluids. Hence the fluid content of the body is replaced via manual, medical means

    • An eye doctor has to be consulted to prevent any damage to the eyes

    • The doctor may use antihistamines to ease itching, topical steroids to alleviate inflammation of the skin, pain killer medications and antibiotics for the control of infection.

    • Skin grafting may be required, if large sections of the body are affected by Stevens-Johnson syndrome.


    Stevens-Johnson Syndrome Pictures


















    Orange Urine

    Orange Urine
    Have you experienced having orange urine?  Urine that has an orange hue has many possible reasons. The orange tint in the urine could be simply caused by food color from drinks or foods recently ingested, or it could be a symptom of a medical condition. 










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    About Urine  


    The process of urination is the body’s way of disposing wastes from the blood and excess water from the body. Urine contains toxins and other water soluble materials that can no longer be used by the body. As urine is expelled, the accumulation of these substances that could be harmful to the body is hence avoided. 


    The appearance of urine is as important as urinating itself. The color of urine can be a good indicator of the health status of an individual. It could provide clues about the substances or materials taken in; whether the body lacks fluids; or if it is suffering from a condition or ailment. 


    Normally, the tinge of urine is yellow which could be attributed to urochrome, the pigment responsible for giving urine its color. Depending on how concentrated the urine is its color ranges from light yellow to dark amber. The lighter the color is, the more hydrated the body is; whereas a deeper color indicates that the urine is more concentrated. 


    However, urine can take on a different shade for various reasons. Urine could present itself as pale yellow, dark yellow, brown, red, milky white and even orange. It doesn’t necessarily follow that a different tinge of urine is indicative of a health problem. Some of the colors are brought forth by the food and drinks ingested; others are due to medications; while others, still could point to an underlying health condition. 


    What are the causes of Orange Urine? 


    In some instances, urine could appear orange. Peeing orange urine has several causes. It could be due to medications, food or food coloring, or certain medical conditions. Usually, the reason behind the coloring is absolutely harmless. However, there are cases in which the orange tint calls for a consultation with a doctor.



    • Food and food coloring


    Certain foods and drinks are naturally deeply colored that the hue seeps into the urine. Foods rich in beta-carotene are known to cause orange tinted pee. Some of the well known foods that could give rise to orange urine are blackberries, carrots, beet, beet soup, and rhubarb. Furthermore, candies, juices, drinks and other food that contain orange dye could result in the individual eliminating orange urine.



    • Drugs


    Some medications, substances and vitamins may give urine its orange tint. Excessive intake of vitamin C, for one, typically results in orange urine. Other substances include senna laxative, beta-carotene supplements, rifampin, phenolphthalein, vitamin B supplements, phenazopyridine and sulfasalzine.











    • Medical conditions


    Orange urine may also be a sign of a health condition. There are a number of medical conditions that has orange-hued urine as one of its symptoms. For instance, the lack of fluids in the body will give the urine a deep yellow to orange color. Hepatitis as well as jaundice exhibit orange urine. Bile in the urine renders it a deep orange to brownish shade. Other medical conditions known to cause orange tint in the urine are urinary tract infections, pancreatic cancer, liver cancer and bladder diseases. Any injury or damage sustained by the urinary tract organs like the ureter, bladder and kidneys could also lead to orange-colored urine.



    What are the symptoms that accompany orange urine? 


    If the orange tint is caused by vitamins, medications, food and food coloring, the urine color will disappear when the said substances are no longer ingested. In such case, no other symptoms are experienced. On the other hand, when orange urine is due to underlying medical conditions, other symptoms will also be exhibited. These vary depending on the root cause of the problem. 


    Some of the symptoms when the problem involves the urinary tract are:



    • difficulty in urination

    • dysuria (burning sensation during urination)

    • frequent urination

    • hematuria (blood tinged urine)

    • murky urine

    • urgency to urinate

    • urine with foul odor


    Meanwhile, jaundice, weight loss, bruising, bleeding, fever, malaise, tachycardia, poor appetite, itchiness of the skin, hypotension, and nausea may also be displayed if the underlying cause involves other systems of the body. 


    Diagnosis


    Seeking immediate medical attention is necessary when the following are present together with orange urine.



    • Fever greater than 101°F

    • inability to urinate

    • intense abdominal pain

    • severe pain in the lower back

    • vomiting


    The doctor will assess your condition and ask you questions like if you’ve noticed pungent odor in the urine, your intake of beta-carotene supplements or fruits and vegetables, if you are on medications and if you experience burning sensation while passing urine.  The doctor may also prescribe tests to ascertain the precise cause.

    How is orange urine treated?



    Treatment of orange urine is based on the root cause. If the change in color is due to dehydration, increase in the intake of fluids is all that is needed to get the color of the urine back to normal. If the orange hue is traced to food and medications, discontinuing or reducing the intake can help solve the situation. However, if the orange shade is caused by a health problem, this has to be addressed properly so that color change in the urine can be resolved.












    Achondroplasia Dwarfism

    Achondroplasia Dwarfism
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    What is Achondroplasia?


    It  is a genetic disorder of bone growth and is the common cause of dwarfism. The literal meaning of Achondroplasia is “without cartilage formation”. Cartilage plays a crucial role in the early development of human beings. However, in children with achondroplasia, cartilage is unable to get converted in bones especially in the regions of arms and legs. It is one of the common forms of disproportionate short stature. Occurrence of achondroplasia is rare as it happens in one in 40,000 live births.










     Causes


    Achondroplasia is caused due to gene alteration in the Fibroblast Growth Factor Receptor 3 (FGFR3) gene. FGFR3 gene makes protein which is involved in converting cartilage to bone. Achondroplasia is mainly caused on people who have only a single copy of the normal FGFR3 gene and a single copy of FGFR3 gene mutation. While it is said to be inherited from parents, in most of the cases it was found that people with achondroplasia has average sized parents. The situation arises when FGFR3 occurs in one of the parent’s eggs or sperm cell before conception. Person with achondroplasia has 50% chances of passing this to the new generations, which means, a person suffering from achondroplasia may not have kids who are suffering from same. On the other hands, parents who are not having this syndrome may have kids who suffer from Achondroplasia. Usually, the new gene mutations which can cause achondroplasia are mainly the result of increased parental age. Mutations of couples with more than 35 years of age have more chances of a kid with symptoms of achondroplasia and as per the studies; they are more likely be inherited from father.


     Symptoms of Achondroplasia


    People with achondroplasia have an abnormal bone growth resulting in short stature affecting mainly the arms and legs. It is observed that the arms and legs are developed disproportionately. Persons suffering from achondroplasia also have a large head, short fingers, toes and a prominent forehead with small midface. The physical structure of the persons with achondroplasia, however, does not have any impact on the intelligence. The IQ of the persons appears to be normal and they also have a good life span. Because of weak muscle tone, infants born with achondroplasia found difficulty in walking and there might be some delays in learning other movements of the body. Spinal cord can be easily compressed which increases the chances of death during infancy. Other common health problems faced by achondroplasia affected persons include frequent ear infections, breathing problems, obesity, and sometimes back pan.


     Diagnosis


    Achondroplasia can be diagnosed by clinical and X-ray findings. Preventative actions can be taken if the disease is diagnosed before child birth. The diagnosis is mainly done with the help of prenatal ultrasound and a DNA test which can be performed before birth of the child to determine the presence of homozygosity. In the condition of homozygosity, two copies of mutant gene are inherited which results in stillbirths. MRIs or CT scan can also evaluate the condition of spinal cord and how much it is compressed. The clinical features of achondroplasia like short limbs, prominent forehead, etc. (as mentioned above) can also be diagnosed at the initial stages. Leading clinical laboratories provide testing of FGFR3 gene mutation. Genetic testing is considered to be one of the best ways to identify mutations.










    Treatment of achondroplasia


    Achondroplasia has no treatments. For preventive measures and not to make the matters worse, children who are born with achondroplasia should have a proper checkup of their height, weight, etc. and parents are required to monitor their growth. More care should be taken during infancy as children born with this deformity have week spinal cord which can even cause death. Persons suffering from achondroplasia are prone to other health problems at early stages. Proper care should be taken to avoid obesity. Sometimes, adenoids and tonsils are removed surgically or a surgical opening is made in the airway. Few people have a myth that infusion of human growth hormone can help for the growth of muscles; however, it is not true. A surgery of limb lengthening can be done, but it is generally not recommended by the doctors. Surgery can also be performed to reduce pressure on the brain. Researchers are now exploring if gene based therapy can be done to treat any future occurrences of achondroplasia.


    Achondroplasia is a non treatable disease. People with the symptoms of achondroplasia should be given enough support from society and they should be made realised that their IQ is normal and they can do normal activities. It is a myth that this condition is inherited as studies showed that over 85% of people with symptoms of achondroplasia have parents with normal structure. However, there is a possibility that if both or one of the couples have achondroplasia, there is a 25-50% chance of gene mutations which will result in dwarf children.


    Achondroplasia pictures


















    Cyanosis

    Cyanosis
    Cyanosis occurs when the blood lacks oxygen causing the skin to appear bluish or purplish. This condition could involve the lips, gums, tongue, nail beds, fingers, toes and mucous membranes. People affected by this could be suffering from some kind of cardio or respiratory disease or blood disorder. The onset of bluish skin discoloration in children or infants can be terribly alarming to parents and so the condition calls for immediate medical evaluation especially when signs of distress are evident.










    People affected by cyanosis are treated based on the underlying medical disorder. Treatment will not only address the problems caused by the underlying disease but prevent permanent damage and life-threatening complications from happening. Without treatment, bluish skin discoloration could mean heart or respiratory failure.


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  • 2 When does Cyanosis need immediate medical attention?
  • 3 What are the forms of Cyanosis?
  • 4 How is Cyanosis diagnosed?
  • 5 Cyanosis pictures

  • Why does the skin turn blue?


    An oxygen-rich blood produces red-pink skin while oxygen-poor blood results in blue-purple skin discoloration. Cyanosis develops due to poorly oxygenated blood. Oxygen is important for healthy cells and tissues and it is transported by hemoglobin. During respiration, oxygen gets into the body through the lungs and the hemoglobin distributes it to the cells and tissues all over the body. Oxygen-poor blood is circulated back to the lungs for replenishment.


    There are several reasons behind the bluish discoloration of the skin and this could involve:




    • Lung problems


    Respiratory problem permits the flow of oxygen-poor blood without getting the needed oxygen for replenishment. This problem could come in the form of severe pneumonia, COPD, pulmonary hypertension, asthma, bronchitis or inflamed bronchioles. In infants, bluish skin discoloration could be due to hyaline membrane disease – a condition that primarily affects preterm babies.




    • Heart defects or abnormalities


    Heart problems may also allow the blood to pass through the lungs without getting oxygen. This could either be due to a blood clot or some form of congenital heart defect.




    • Blood abnormalities


    Blood disorders drastically impair oxygen absorption resulting in cyanosis. These disorders could involve excessively high levels of abnormal hemoglobin or Raynaud’s phenomenon – a condition in which the small arteries in the toes and fingers constrict, preventing blood to circulate.


    Several other things can also cause the bluish discoloration of the skin, like prolonged seizures, cold exposure and drug overdose. Cyanosis is actually a symptom of an underlying medical issue than a disorder in itself.


    When does Cyanosis need immediate medical attention?


    Bluish skin discoloration should not be ignored because it could be indicative of life-threatening conditions such as cardiopulmonary arrest, congestive heart failure and pulmonary embolism. The first 5 minutes is very crucial for immediate medical intervention and patients should be taken to the nearest hospital if cyanosis is accompanied by:



    • Breathing difficulties

    • Chest pain

    • Shortness of breath

    • Grunting

    • Confusion


    Also, parents should never delay bringing their babies to the hospital if the child is also irritable, fussy, difficult to feed and lethargic.










    What are the forms of Cyanosis?


    The difference between the two forms of cyanosis has something to do with the part of the body where bluish discoloration is noted. Cyanosis can be peripheral or central.



    • Peripheral


    As the name suggests, the bluish discoloration is noted on the peripheral parts like the nail beds, fingers, arms, toes and legs. The extremities receive oxygen-poor blood due to slow blood circulation to the limbs. This could also be attributed to constricted small blood vessels. There is no lung or heart failure involved is this form of cyanosis.



    • Central


    This is a serious form of bluish skin discoloration that causes bluish tongue and lips. It may or may not occur with bluish toes and fingers. There might be lung or heart involvement or high level of abnormal hemoglobin.


    How is Cyanosis diagnosed?


    The doctor will run several tests to determine the cause of the bluish discoloration of the skin. This may involve a series of blood work, X-ray, and echocardiogram. The doctor may also request for cardiac catheterization and monitor the oxygen saturation.


    Treatment is primarily targeted towards replenishing the lacking oxygen in the blood. The underlying cause will also be treated. Tissues will eventually die if there is a lack of oxygen in the blood. Treatment may involve:



    • Warming


    Warming could be all that is needed to treat bluish fingernails and toes as this will promote blood circulation to the extremities.



    • Oxygenation


    Oxygenation is done in combination with other strategies to increase the amount of oxygen in the blood, such as the use of breathing machine, ventilator, medication and substances that contain oxygen.



    • Surgery


    This is commonly done in patients with congenital heart defects. Babies born with congenital heart defects are placed on breathing machines to support breathing. Surgery could be done immediately after birth or months or a few years after.


    Babies born with heart problems must receive up-to-date immunizations and monitored by the doctor regularly. Older patients may require permanent pacemaker to normalize the heart rate. People suffering from heart problems may also need diuretics and medicines to cause the heart to pump harder. Respiratory infections are also treated using antibiotics.


    Cyanosis pictures















    Trisomy 13 – Life Expectancy, Symptoms, Causes, Treatment, Pictures

    Trisomy 13 – Life Expectancy, Symptoms, Causes, Treatment, Pictures
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    What is Trisomy 13?


    Also known as Patau Syndrome, Trisomy 13 is a genetic disorder in which the person gets three copies of chromosome 13, which in normal cases is two copies. This extra copy of chromosome may cause neurological and heart defects making it challenging for infants to survive.










    Based on extra DNA from chromosome 13 present in some or all body cells, Trisomy 13 can be further classified into following types:


    i.                              Trisomy 13- When DNA from chromosome 13 is present in all body’s cells.


    ii.                             Trisomy 13 mosaicism- When DNA from chromosome 13 is present in some of the cells.


    iii.                            Partial trisomy – When only a part of third chromosome is present in the body cells.


    The occurrence of this syndrome is least common among the three autosomal trisomies: Trisomy 21, Trisomy 18 and Trisomy 13. Patau Syndrome usually affect females more than males because of the fact that male fetus having this syndrome could not survive till birth.


    Trisomy 13 is found in every 1 of 10,000 babies born. Trisomy 13 is associated with the age of the mother and can affect people of any background. Generally Patau syndrome is not passed down through heredity but the syndrome occurs due to abnormalities in sperm or egg during fetus formation.


    Trisomy 13 life expectancy


    More than 80% of the children born with Trisomy 13 die within the first year. Sad but true, prognosis for child born with Trisomy 13 is very less but such babies are still born. Some babies with Trisomy 13 will survive the pregnancy and some of the babies survive only their first month of birth. However it becomes difficult to predict the life expectancy of a child born with Trisomy 13 if no life threatening problems exist at the time of birth. In rarest of the rare case, the child may survive teenage as well.


    Causes


    In a normal case, sperm and egg unite at the time of fertilization to form 23 chromosome pairs or 46 chromosomes. However abnormality occurs when sperm and egg are forming and an extra chromosome i.e. chromosome 13 is released to the embryo. This extra chromosome can come either from father’s sperm cell or mother’s egg cell.


    Sometimes chromosome 13 is already attached to another chromosome in the sperm or egg. This condition is also known as translocation. If this occurs, trisomy 13 is inherited in the family.


    Trisomy 13 Symptoms


    The symptoms of characteristics of Trisomy 13 include:


    •             Polydactyl i.e. extra toe or finger may be present


    •             Clenched hands


    •             Small eyes or eyes may fuse into one another to form close-set eyes


    •             Reduced muscle tone


    •             Umbilical and Inguinal hernia


    •             Split, cleft or hole present in the iris.


    •             Scalp defects including missing skin on the scalp


    •             Micrognathia- small lower jaw


    •             Cryptorchidism – undescended testicle


    •             Seizures and limb abnormalities


    •             Rocker bottom (deformed) feet


    •             Heart and kidney defects










    •             Neurological defects- microcephaly i.e. small head, holoprosencephaly i.e. brain doesn’t divide into two during gestation period and mental problems.


    •             Other facial defects- Microphthalmia i.e. small eyes, deformed nose and cleft palate or lip.


    Diagnosis


    The symptoms of Trisomy 13 are evident at the time of birth. It has been reported that sometimes Trisomy 13 is mistaken with Trisomy 18 which can be prevented by conducting genetic testing. Usually computed tomography and magnetic resonance imaging are done to detect the condition of heart, brain and kidney. Echocardiogram which is an ultrasound of heart can be done to know more about associated heart defects.


    Gastrointestinal X-ray and ultrasounds can be done to detect the rotation of internal organs. Chromosome studies can be conducted to know whether it’s partial, full or mosaicism.


    Trisomy 13 treatment


    Treatment of Trisomy 13 depends on individual developing the kind of abnormality from this syndrome. It is seen that in most of the cases infants have problem in surviving the first few weeks owing to severe heart and neurological problems. For facial deformations like cleft lip or cleft palate and for heart defects, surgery is required.


    Also, physical and speech therapy help the patients in attaining full developmental potential to a great extent.


    Prognosis and complications


    Trisomy 13 is associated with a number of complications which begin immediately. Some of the complications include:


    •             Congenital heart disease


    •             Problem in feeding


    •             Seizures


    •             Deafness


    •             Difficulty in breathing or breathlessness


    •             Vision problems


    •             Heart failure


    If you see any symptom of Trisomy 13 in your child, see your health care provider immediately. Also if you already have one child with Trisomy 13 and you are planning for the next child, you should see the doctor first. Genetic counseling can help a great way in understanding the condition and ways to prevent risk of inheriting it further.


    Prevention


    Trisomy 13 is a genetic disorder and is difficult to prevent. But it can be diagnosed before birth by amniocentesis. Parents with Trisomy 13 should get genetic testing and counseling done to know the likelihood of their baby developing this condition.


    Trisomy 13 pictures