Thursday, June 12, 2014

White Spots in Throat

White Spots in Throat
White spots in throat are caused by an infection of your tonsils. Tonsils are located at the back of the throat, and they have a gland-like appearance. Tonsils play a vital part in keeping bacteria out of your body. They do this by capturing any bacteria and viruses that enter through your mouth thereby preventing infection. Tonsils have a pitted appearance, due to small pockets, or divots, known as tonsil crypts. Saliva mixes with the soft tissue that lines the tonsil crypt. A trapped food in the tonsil crypts is broken down by saliva. As the starch and carbohydrates are broken down, they mix with mucus and bacteria. The resultant mix, will over-time, become concentrated, harden, and calcifies to become tonsil stones. The condition is called cryptic tonsils, since the stones form in the crypts of the tonsils. These stones are usually very small in size, but they can become large, with time. If you were to take a flashlight and shine it down your throat, you will see the stones, which appear as white spots. If you suffer from cryptic tonsils, you will always have a feeling like there is something stuck at the back of your throat.











The main causes of tonsil stones, and called tonsiliths are:











  • Hyperactive salivary glands

  • Oral bacteria

  • Mucus deposits

  • Trapped food


Symptoms of White spots in throat



  • Bad Breathe – Cryptic tonsils cause you to have bad breathe. However, it does not mean that whenever you have bad breathe, you are suffering from cryptic tonsils. If you maintain good oral health, through regular brushing, and using mouth wash, and the rotten egg smell persists, then you may be suffering from the condition. The reason for this is the amount of bacteria that is trapped in the ever-enlarging tonsil stones. The smaller stones will not make a huge difference in your life, but larger stones can cause you a lot of embarrassment and discomfort. If you have ever coughed and emitted a smelly, white stones, then you are suffering from this condition.

  • White-yellowish spots or lumps that appear at the back of the throat.

  • A tonsil infection may also occur.

  • You will develop a sore throat, and find it difficult to swallow.

  • You will experience a bad taste at the back of your throat, or the roof of your mouth.

  • The tonsils may swell due to inflammation caused by the stones.

  • You will develop a serious itch in your ear, which may be accompanies by an ear ache. This is because the stones affect connected nerves.


Most people think that they are the only ones suffering from this condition, and keep quiet about it. They seek remedies for halitosis (Bad Breathe), but the condition persists. There are several ways that you can treat this condition, and these are:


Treating White spots in throat


The treatment of cryptic stones is not difficult, and can be done without medication.  In order to dislodge the stones, you can use organic apple cider, and gurgle 3 or 4 times a day. You may also use two tablespoons of vinegar mixed with warm water. Salt if a natural antiseptic and gurgling a brine solution will help remove the stones.












Symptoms of Anemia in Children

Symptoms of Anemia in Children
Anemia is a disorder characterized by the lack of adequate healthy red blood cells to distribute oxygen-rich blood to different organs and tissues in the body. The presence of anemia may result in a feeling of perennial exhaustion. A large percentage of children in the United States are affected by anemia.










There are several types of anemia and each has a specific cause. One of the most common causes of anemia is loss of blood. Anemia can be chronic or short-term, and it can vary from minor to serious.


Consult a doctor if you feel that your child has anemia, because it can be a symptom of a serious underlying condition. Treatment for anemia can include varied medical procedures, consuming supplements, etc. It is possible to prevent certain forms of anemia in children by opting for a varied and healthy diet.



Symptoms of anemia in children


The signs and symptoms of anemia in children may differ as per the cause. However, common symptoms include:



  • Exhaustion or fatigue

  • An irregular or rapid heartbeat

  • Paleness of skin

  • Breathlessness

  • Dizziness

  • Pain in the chest

  • Cognitive difficulties

  • Headaches

  • Cold feet and hands


The initial symptoms of anemia in children may be so mild as to go unnoticed. The symptoms however increase with worsening of the condition.


Untreated cases of anemia can result in a number of medical complications such as cardiac problems, elevated fatigue, and even death.


Causes of anemia in children


Anemia occurs due to insufficient number of red blood cells in the bloodstream. This may be caused due to:



  • Inadequate production of RBCs by the body

  • Destruction of red blood cells by the body

  • Bleeding. It results in rapid loss of RBCs which cannot be as quickly replaced by the body.


Functions of red blood cells: The body produces three kinds of blood cells, i.e., RBCs to supply oxygenated blood across the body, white blood cells to defend against infections, and platelets that aid in blood clotting.











  • RBCs contain hemoglobin which is an iron-abundant, red protein that imparts the red color to blood. Hemoglobin enables RBCs to carry oxygen from the lungs to different areas of the body, and to carry back the carbon dioxide from across the body to the lungs, so that it can be removed during exhalation.

  • A majority of blood cells, including RBCs are regularly made by the bone marrow. The body requires vitamin B-12, iron, folate, and other essential nutrients from the consumed food to be able to produce RBCs and hemoglobin.


Common types of anemia in children and its causes



  • Vitamin deficiency anemia: If the diet of children lacks vitamin B-12, folate, and other major nutrients then it can lower the RBC production. Also, despite sufficient intake of B-12 some children may still develop vitamin deficiency anemia as their bodies cannot process the vitamin.

  • Iron deficiency anemia:It is caused due to lack of iron element in the body. The bone marrow cannot produce sufficient hemoglobin for RBCs without enough iron. This type of anemia is usually caused due to loss of blood, via cancer, heavy menstrual bleeding, a polyp in the digestive system, an ulcer, or prolonged use of NSAIDs or aspirin.

  • Anemia caused by underlying chronic disease:HIV/AIDS, cancer, Crohn’s disease, prolonged inflammatory diseases, rheumatoid arthritis, and other chronic diseases can affect the production of RBCs, thereby causing chronic anemia in children. Kidney failure is another major cause.

  • Anemia related to bone marrow diseases: Myelodysplasia, leukemia, and other such cancer-like conditions can affect the production of blood by bone marrow. Such diseases can cause mild changes in the production of blood, or a complete and fatal shutdown of the blood-production process. Myeloproliferative abnormalities, multiple myeloma, lymphoma and other cancers of the bone marrow or blood can also cause anemia in children.

  • Aplastic anemia: It is a very rare and deadly type of anemia that is caused due to lowered ability of the bone marrow to make RBCs. The condition may be caused due to drugs, infections, and autoimmune disorders.

  • Sickle cell anemia: It is a hereditary and occasionally severe form of anemia that affects children. It is caused by an abnormal hemoglobin type which forces RBCs to take an anomalous crescent or sickle shape. Such irregularly-shaped RBCs tend to die prematurely, thereby leading to a perennial dearth of red blood cells.

  • Hemolytic anemia: It causes destruction of RBCs at a rate that is faster than the rate of replacement by the bone marrow. RBC destruction may be caused due to some underlying blood diseases. Hemolytic anemia can be hereditary, or it can develop later.


Treatment of anemia in children


Anemia in children is treated as per the underlying cause of the condition.



  • Vitamin deficiency anemia in children can be treated by increasing the percentage of vitamin C and folic acid in the diet and via dietary supplements. Vitamin B-12 injections are given to children whose digestive systems are unable to absorb the vitamin from the consumed food.

  • Iron supplements and diet changes can help treat iron deficiency anemia in children. If it is caused due to blood loss, other than menstruation, then the cause of bleeding has to be stopped via surgery or other means.

  • Chronic disease anemia is treated by curing the underlying cause. Severe cases may require synthetic erythropoietin injections or blood transfusions.

  • Bone marrow disease associated anemia can be treated with simple drugs, chemotherapy, or transplantation of bone marrow.

  • Blood transfusions and bone marrow transplantation are available treatment options for aplastic anemia in children.

  • The treatment of sickle cell anemia may include use of pain killer medications, oxygen administration, and intravenous or oral intake of fluids, to alleviate pain and prevent health complications.Physicians may also suggest antibiotics, blood transfusions, and folic acid supplements. In some cases, bone marrow transplantation may also prove to be very effective. Patients may also be given a cancer medication known as hydroxyurea for treating this type of anemia.

  • Treatment of hemolytic anemia involves curing associated infections, avoiding suspect drugs, and intake of immuno-suppressant medications. Plasmapheresis and blood transfusions are other treatment options.












Hypoxia – Types, Symptoms, Causes, Treatment

Hypoxia – Types, Symptoms, Causes, Treatment
Hypoxia refers to deficiency in amount of oxygen reaching the body tissue and it differs from hypoxemia is that the latter is an inadequate amount of oxygen that travels in blood. Hypoxemia can contribute to hypoxia in that when there is an inadequate amount of oxygen in blood, it can lead to insufficient oxygen reaching the tissues. When there is complete lack of oxygen in tissues, this is termed as anoxia or oxygen starvation. When hypoxia occurs, it can affect the whole body a situation known as generalized hypoxia.










However, if it affects a specific organ or part of the body, it is called tissue hypoxia. In addition, the condition can be termed as acute or chronic in which acute means a rapid onset. Chronic means that the condition occurs over time and slowly. When variations in oxygen concentration within the arteries occurs, it can cause deprivation of sufficient adequate oxygen supply in tissues or the whole body such as witnessed during a physical exercise.


Moreover, a mismatch between the demand of oxygen and its supply at the cells or cellular levels may as well lead to hypoxia. Often, confusion occurs in use of the terms hypoxia and hypoxemia since they are both related to oxygen levels but hypoxemia involves abnormally low concentrations of oxygen within the arterial blood.


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What are the different types of hypoxia?


There are different types of hypoxia and they include hypoxic hypoxia, hypemic hypoxia, histotoxic hypoxia, and ischemic hypoxia. To elaborate these terms, hypoxic hypoxia simply refers to generalized insufficient oxygen supply in the whole body. In hypoxic hypoxia, the tissue does not receive sufficient oxygen since there is inadequate amount or concentration of oxygen in blood that flows to the tissues.


High altitude can trigger episodes of hypoxic hypoxia because of the low partial pressure of the atmospheric oxygen. When the atmospheric oxygen pressure is modified in an environment such as a sewer line, it may create the condition. Other causes of hypoxic hypoxia are such as a low partial pressure in oxygen created in lungs as a person switches to atmospheric air from an inhaled anesthesia. This is termed as diffusion hypoxia or the Fink effect.


Another cause of hypoxic hypoxia is a reduced oxygen saturation that is caused by hypopnea or sleep apnea. Chronic obstructive pulmonary disease- COPD, may cause inadequate pulmonary ventilation, which leads to hypoxic hypoxia. In hypemic hypoxia, the total oxygen content in blood reduces though the arterial oxygen pressure remains normal.


Histotoxic hypoxia occurs when there is adequate concentration of oxygen from the lungs that is delivered to tissues but the cells are not able to make use of it. Although oxygen is supplied sufficiently, the cells are unable to utilize it in their metabolic activities due to disabled oxidative phosphorylation enzymes and this situation is commonly witnessed when a person drinks alcoholic beverages.


Stagnant or ischemic hypoxia occurs due to inadequate blood flow. There is local restriction in the circulation of otherwise sufficiently oxygenated blood. This may be caused by ischemic heart disease, and cerebral ischemia.











Causes of hypoxia


Causes of hypoxia differ in one way or another and while the condition may be caused by lung disease, environmental conditions may also contribute to the condition. High altitude creates difference in atmospheric oxygen pressure creating partial oxygen pressure, which can cause insufficient amount of oxygen in body tissue.


When the lungs are affected by health conditions like asthma, COPD, pneumonia, lung cancer, pulmonary hypertension, and rheumatoid lung disease, these conditions can create hypoxia. Not breathing enough or hypoventilation situation can cause the reduced amount of oxygen in body tissue. Hypoventilation may be central where the brain does not stimulate the lungs to breathe as witnessed in anesthesia use, effects of stroke, or trauma caused by a head injury.


Side effects of certain medications such as those used to treat pain may cause hypoventilation. Illegal drugs can also cause changes in the function of brain in stimulating the lungs to breath. Peripheral hypoventilation may occur when there is obstruction of airways, which interrupts breathing for example, choking caused by large foreign objects that lodges to the trachea. Drowning, cardiac arrest, and suffocation may also result to hypoventilation.


A patient with anemic hypoxia may also have problem of insufficient oxygen in tissues. When poisoning occurs from carbon monoxide, the hemoglobin is not able to bind oxygen molecules properly causing lack of utilization of oxygen. Moreover, if there is obstruction of the vessel carrying oxygenated blood to tissue by a clot, as may happen in a heart attack, such a condition may cause ischemic hypoxia. This prevents the tissues from receiving oxygen. 


Symptoms of hypoxia


There are different symptoms and signs experienced by people who suffer from hypoxia and they include dizziness and fainting, dyspnea or shortness of breath, headache, lethargy, confusion and lack of judgment. A rapid heart rate may be witnessed as well as elevated blood pressure or hypertension.


A tingling warming sensation, loss of coordination, tunnel vision, increased levels of red blood cells count in chronic hypoxia are other symptoms experienced by a person. The extremities and lips may suffer from bluish tinge or discoloration of skin, a condition known as cyanosis. Hypoxia affects organs like the liver, brain, and heart. With severe hypoxia, it can cause irreversible damage within a short time after its onset. Seizures, coma, and death could also occur. Chronic but milder hypoxia may also result to damage in organs of the body with time.


Treatment of hypoxia


The treatment of hypoxia largely depends on the causal factor. When you are short of breathe, oxygen therapy may be recommended while the real cause of the condition is determined for more specific and appropriate treatment. In case of effects of high altitude sickness or condition, oxygen enrichment may help counteract hypoxia. This may include increasing the concentration of oxygen in air by use of oxygen concentrators. Mechanical ventilation may be applied if symptoms of hypoxia are severe with use of a ventilator. If hypoxia is caused by blockage of blood vessel leading to the brain, then the clot or hardened vessel is treated. Similarly, if the hypoxia is caused by tumor in lungs, then the removal of the tumor can help relieve the condition.












Lower Abdominal Pain in Women

Lower Abdominal Pain in Women
Every woman experiences lower abdominal pain at some point in their lives. In order to lessen the pain,a patient should know the type of pain,its symptoms, and the underlying cause of the pain. This way affected women can ease the pain and know how to remain healthy. Some of the common causes for lower abdominal pain in women are periods, and urinary disorders like kidney or bladder infection. Improper functioning of the reproductive system such as ovaries, fallopian tubes and uterus also result in stomach pain. A doctor should know all the details about the pain so that he/she can diagnose the cause accurately; which is not very easy. After diagnosing the cause the medical expert will be able to prescribe the correct treatment.










Usually there are two types of pain, gradual pain and sudden pain. In gradual pain, the pain starts slowly, aggravates and becomes severe, and then gradually becomes less. Such pain is experienced by women when suffering from gastroenteritis, renal colic or functional bowel syndrome. In sudden pain, unexpected intense pain occurs in the lower portion of the abdomen. Such pain occurs due to many reasons for which signs and symptoms have to be studied.


Causes of lower abdominal pain in women


The varied causes of lower abdominal pain in women due to the disorders in the urinary systemare as follows:



  • Infections in kidney like pyelonephritis can result in high fever and severe lower abdominal pain.

  • Another cause for pain in stomach is kidney stones. This pain further spreads to other parts of the body.A doctor should be consulted right away if burning sensationsare felt while urinating and which is accompanied by back pain. Some other symptoms like constant feeling of vomiting may also occur.


The different causes of lower abdominal pain in women due to the disorders of the reproductive organs are as follows:



  • In ectopic pregnancy fertilized eggs get implanted outside the uterus. This results in lower abdominal pain and also vaginal bleeding.

  • Womb stones also known as fibroids are abnormal growth in the uterus. When womb stones or fibroid occurs, they cause pain in lower abdomen. Some other symptoms a woman may experience when suffering from fibroids are irregular or excess bleeding during menstruation.

  • One common cause for lower abdominal pain is ‘endometriosis.’It is a disease where the cells of endometrium develop on the exterior portion of the uterine cavity and pain caused due to this increases during periods.

  • A cyst in the ovaries is a fluid filled bag which can be treated with medicines and surgeries. This also causes pain in lower abdomen.

  • Bacterial infections of the ovaries, fallopian tubes and uterus also lead to lower abdominal pain in women and vaginal discharge.


Some other causes of lower abdominal pain in womeninclude:











  • Abdominal aortic aneurysm:This condition occurs when the abdominal aorta bursts and starts to leak because of some medical complications. The abdominal aorta is the blood vessel that carries blood to the abdomen from heart.The condition results in severe abdominal pain in the middle portion which later shifts to the lower abdomen and then to the back. Normally, it is treated via surgery.

  • Cancer: Cancerous growth of tissues in the bellyleads to pain in lower abdomen in women. Some of the symptoms are loss of appetite and weight, constipation, and feeling of sickness. In such a case doctor should be consulted at the earliest.

  • Diverticulitis: Inflammation of diverticula results in diverticulitis. Diverticula arefound on the exterior of the colon. Usually elderly women over sixty years of age suffer from diverticulitis which causes lower abdominal pain.

  • Constipation:Constipation, whether severe or not, gives rise to pain in the lower portion of the abdomen. This pain starts after defecation. Walking and drinking plenty of water can helpstimulate the passing of stool. But if it does not work then medical expert should be consulted immediately. Some accompanying symptoms are bloating and swelling.

  • Diarrhea: Diarrhea is also one of the causes for lower abdominal pain in women. As with constipation, pain associated with diarrhea is temporary; it comes and goes quickly.

  • Many women suffer from irritable bowel syndrome which also causes back pain and lower abdominal pain.


Treatment for lower abdominal pain in women


Women must consult a doctor whenever they experience prolonged instances of lower abdominal pain. The physician may do the following:



  • He/she will want all details about the pain, other information related to menstruations, bowel habits, and also details about accompanying symptoms like nauseated feeling, vomiting, or fever.

  • If necessary, the doctor may also require details about the patient’s family history, personaland professional life, and her intimate relations.

  • After collecting all the details, the doctor will check and tests will be conducted internally and externally. Usually, a urine test will also be taken to check for infection. In some cases doctors may check some vaginal swabs too. Occasionally, a specialist has to be consulted for ultrasound of the abdomen.

  • Once the tests come the doctor will advise further tests if needed, else prescribe the correct treatment.












Williams Syndrome

Williams Syndrome
Williams syndrome is a rare genetic disease. It is identified by the occurrence of serious medical problems such as presence of compressed arteries that cause cardiovascular diseases. High levels of calcium in blood may also be found in patients when they are infants. A person suffering from Williams syndrome experiences learning difficulties, and a unique attitude that includes anxieties, and excessive compassion and friendliness. The patient may be suffering from mild to severe mental retardation.










Williams syndrome occurs due to a random genetic change which causes removal of a small part of chromosome seven. Therefore, it is not hereditary. However,a person with the syndrome carries a high risk of about fifty percent of passing this disorder to the child.


Unfortunately no proper cure for Williams syndrome is known as yet. Also, no defined treatments are available. It is an uncommon and complex disorder for which different medical experts have to be consulted and then plan for effective cure.


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Symptoms of Williams syndrome


The signs and symptoms of Williams syndrome may differ from person to person; some may show mild symptoms whereas some may show very severe signs. The treatment is done as per the level of symptoms. Therefore it is necessary to study them.


Some of the signs and symptoms of Williams syndrome are as follows:



  • Presence of ADD or Attention Deficit Disorder in the patient. The patient may also suffer from poor concentration abilities and become unfocused very easily.

  • Poor speech development or delay in speech or language. However, after some time it may change into good speaking capabilities with good learning through hearing.

  • Mental retardation may vary; it may be mild to moderate.

  • The small finger may be twisted inwards

  • Some personality featuresare very visible, such as over-affability, extra interest in music, trusting strangers, and dread of physical contact or piercing sound.

  • Patient may not have as good a height as compared to other family members

  • Learning disabilities

  • The patient may have a hollow chest

  • A person suffering from Williams syndrome may not have a regular facial appearance. Some other unusual features are:

    • The interior part of the eye is usually covered by skin folds

    • The bridge of the nose is flat. It is wrong side up

    • Long folds that start at the nose and end at the upper lip is visible

    • Teeth might be tiny or not properly spaced, away from each other or absent as well. Some flaws are visible in the tooth enamel




At times few complications may arise because of Williams syndrome:



  • Constriction of arteries may result in cardiac failure

  • In very rare cases, the patient might die because of anesthesia

  • Excess calcium in the kidney and kidney disorders

  • Excess pain in abdomen


When a child is born, symptoms of Williams syndromeare not visible. If any of the signs and symptoms are noticed by parents or a health care giver, then a specialist should be consulted immediately. If a member of the family has suffered from Williams syndrome then it is better to go for genetic counseling before planning for a baby.










Causes of Williams syndrome


Williams syndrome is a rare disorder and it occurs because some genes are not present, i.e., the genes are absent. This condition occurs by chance. Even though none of the parents have this condition,their child may suffer from Williams syndrome. Also, if any of the parents do have this disorder then there is fifty percent chance that the baby may also develop this genetic mutation.


One amongst the twenty five genes that are lost or mutated is the gene that develops a protein called as ‘elastin.’ The main function of elastin is to allow a variety of blood vessels and tissues in the body to expand and elongate. The absence of one copy of this gene is said to result in narrowing of the arteries, which is a characteristic feature in Williams syndrome patients. The occurrence rate of this disorder is around one in about eight thousand births.


Treatment of Williams syndrome


No proper cure has been discovered as yet for Williams syndrome. Still treatment methods are adopted to alleviate and correct the signs and symptoms of Williams syndrome. Some of the precautionary measures and treatments are as follows:



  • If a patient is suffering from speech disabilities then speech therapy is advised to improve their language and speech

  • Excess intake of calcium and vitamin D should be avoided. If patients have high amount of blood calcium then doctor would treat as per the particular level of calcium to control it.

  • To loosen the stiffness of joints doctor may recommend physical therapy. This will lessen the symptoms of stiff joints.

  • Constricted arteries cause cardiovascular disorders. This constriction may be high or low. The patients are treated as per the condition whether it is mild or severe. If medicines do not work then another option, i.e., surgery is recommended.


Life Expectancy in Williams Syndrome Patients


The life expectancy in patients with Williams Syndrome is lower than that of a healthy individual. Also, these patients need continual care and support. Close to 80 percent of cases show some degree of mental disorder.


Williams Syndrome Pictures



 















Herpetic Whitlow

Herpetic Whitlow
Herpetic whitlow is a skin disorder which affects the fingers and is caused by herpes simplex virus. The condition starts as tiny, red, elevated spots on the skin which deteriorates and turns into a distressing lesion. Patients of herpetic whitlow often experience severe pain which can cause interruption of daily activities.










Herpetic whitlow can be caused by either HSV-1 or HSV-2. It affects both the genders as well as any age group that come into contact with this virus. The incidence rate for herpetic whitlow in the United States is rare and can be seen in 5 out of 100,000 people.


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Symptoms of herpetic whitlow


The symptoms of herpetic whitlow tend to develop over a course of 2 to 20 days, after initial contact with the virus. Some of the signs and symptoms of herpetic whitlow are as follows:



  • Exhaustion, fatigue, and flushed state are the first symptoms of herpetic whitlow

  • Patients may then feel unusual symptoms and physical discomfort of the infected finger

  • In most cases, the physical pain will be followed by formation of blisters after about a week. These blisters comprise of fluids which burst open and result in sores.

  • Most patients recover from herpetic whitlow after 2 or 3 weeks

  • The lymph nodes present below the armpits may elicit abnormal tenderness.

  • Most cases of herpetic whitlow show symptoms similar to other herpes virus infections. The skin condition is most prone to recurrence when the patient experiences ill health in the future. After a successful recovery from herpetic whitlow, the virus moves to Schwann and peripheral ganglia cells and remains dormant. As opposed to first time infections, a recurrent cases of herpetic whitlow are less discomforting. They also resolve faster.


Causes of herpetic whitlow


There are two kinds of HSV, i.e. herpes simplex virus type 2 (HSV-2) and herpes simplex virus type 1 (HSV-1). HSV-2 infections generally affect the genitals or the buttocks, while HSV-1 infections typically appear around the nose, lips, mouth, or face. It may also be noted that HSV-2 can sometimes affect the nose, lips, mouth or face, while HSV-1 can occasionally affect the buttocks or the genitals.


Two forms of infections, i.e. primary and recurring, are caused by both kinds of HSV. The extremely contagious nature of the virus means that a majority of individuals who come into contact with the virus end up with a primary infection. It may also be noted that only about 20 percent of the individuals with primary HSV infections eventually develop noticeable sores and blisters.


Individuals may develop cases of herpetic whitlow are they are exposed to parts of the body which are infected by the herpes simplex virus. Such infections may be present on some other person, on one’s own body.The virus generally enters the body via a tear in the skin, such as a broken cuticle at the lower end of a fingernail. The virus will then establish the infection across the finger tissue. About sixty percent of herpetic whitlow cases are caused due to HSV-1 infections, while the rest 40 percent are caused by HSV-2.










There are some triggers which can cause a dormant virus to become active and return to the skin. The triggers include exposure to sun, illness or fever, stress, hormonal changes like those observed during pregnancy or menstruation, surgery, or trauma. Recurring cases of herpetic whitlow may never occur, or they may recur after every few weeks.


It may be noted that herpetic whitlow can occur in individuals of all races, genders, and ages. However, it is more widespread in children and medical and dental professionals.



  • Children often get affected by herpetic whitlow due to the act of finger or thumb sucking, when a herpes infection in present in their mouth or lips.

  • Medical or dental professionals may get affected by herpetic whitlow due to contact with the contagious blisters of a patient with HSV infection.

  • Health care providers and children generally contract herpetic whitlow due to HSV-1 infections, while others may develop the condition due to HSV-2 infection.


Treatment of herpetic whitlow


Herpetic whitlow is a self-limiting condition and generally disappears on its own after a few weeks. Patients may follow the below listed self-care guidelines to treat the skin disorder:



  • Painkillers may be taken to alleviate the pain as well as to reduce the fever.

  • Application of ice packs or cool compresses may also help ease the discomfort and the swelling.

  • As herpetic whitlow is very contagious, patients should follow certain steps to prevent the transfer of the virus either during the initial stages or during the active stage. Patients should avoid popping the blisters or sharing their personal items with others. They should also cover the affected digits with a bandage.


Medical care for herpetic whitlow includes:



  • Antiviral medications can stop the infection from spreading to other parts of the body.

  • Prescription pain killers may be used for severe pain

  • Secondary infections of the blisters and sores can be treated with antibiotics 


Herpetic Whitlow Pictures


Photos and images of Herpetic Whitlow















Signs of heart attack in women over 50

Signs of heart attack in women over 50
Heart attack is one of the major causes of mortality in women over 50 years of age. It may also be noted that women take a longer time than men to identify and seek treatment for heart attacks and other cardiac conditions. Listed below are signs of heart attack in women over 50 which will help in prompt diagnosis and timely treatment.











Signs and symptoms of heart attack in women over 50


The symptoms of a heart attack differ as per gender. A heart attack in both men and women is usually accompanied by breathlessness and chest pain. Women over 50 may also suffer from the below listed signs of a heart attack:



  • Pain in chest: Women affected by a heart attack often do not elicit intense chest pain. They may experience mild tightness or pressure in the chest. They may also elicit discomfort or burning or squeezing sensations in the chest.

  • Breathing problems: Affected women may experience sudden instances of breathlessness.

  • Pain in the arms: Women over 50 who suffer from heart attack are most likely to experience pain in the arms. The pain will develop in the left part of chest and then migrate to the arms, the shoulder blades, neck, and back. Pain in jaw, shoulders, and the right arm may also be observed.

  • Fatigue: Fatigue or lethargy may also occur without any known underlying cause. Such fatigue may commence many days or even weeks before the cardiac arrest.

  • Increased perspiration: Heart attack patients may also sweat excessively for no apparent reason. This symptom is usually experienced in addition to the above listed signs.


Other signs of heart attack in women over 50 are as follows:











  • Irregular heartbeat

  • Heartburn

  • Anxiety

  • Vomiting or nausea

  • Weakness

  • Dizziness

  • Lightheadedness or loss of consciousness

  • Lethargy

  • Coughing

  • Indigestion

  • Chills


Causes of heart attack in women over 50



  • Heart attacks in both women and men are generally caused due to obesity, hypertension, and excessive cholesterols levels.

  • Low estrogen levels after menopause can also increase the risk towards conditions of the smaller cardiovascular vessels

  • Depression and stress will usually cause adverse cardiac abnormalities in more women than men. Depression can pose problems in following the recommended remedies or in maintaining a healthy lifestyle.

  • Metabolic syndrome, alcoholism, smoking, diabetes, and low levels of physical activities also contribute towards development of a heart attack in more women over 50, than men.

  • Women with a family history of cardiac disorders are also at greater risk to heart attacks.


Treatment and prevention of heart attack in women over 50



  • A heart attack is an emergency situation. After diagnosis, a doctor may treat the underlying cardiac condition via stenting, drug therapies, or angioplasty.

  • As women over 50 are at greater risk to heart attacks and other cardiac abnormalities, they should go for regular medical checkups

  • A healthy diet that consists of fresh vegetables and fruits, seeds, and nuts; lifestyle changes such as limiting the intake of alcohol and quitting smoking; and intake of prescription hormone medications will also help prevent heart attacks.

  • Women over 50 should also maintain a healthy weight and hence exercise at least five days a week. Walking, jogging, swimming, and aerobic exercises are recommended.