Thursday, June 12, 2014

Alice in Wonderland Syndrome

Alice in Wonderland Syndrome
Alice in Wonderland syndrome occurs when there is disorientation of a person’s perception. It is a neurological condition associated with the signals communicated to the brain from the eyes causing distorted perception. Alice in Wonderland syndrome is also known as Todd’s syndrome. When the signals from the eyes to brain are distorted, a person can experience symptoms like loss of sense, alterations of self-image, and hallucinations.










Many patients with this condition are able to grow out of it by the time they get to teenage age, but some of the symptoms may be experienced throughout the lifespan particularly during the time of sleep onset. A person with Alice in Wonderland Syndrome may complain of auditory, visual, and tactile hallucinations coupled with distorted perceptions.


A person may also experience distorted touch perception where one feels as though the ground is spongy right under the feet. This happens because the sensation experienced from touching or feeling something is unrecognized or it is incorrect. Distorted sound perception may also be experienced. This condition can make a patient become baffled and terrified with a feeling of going mad because of the hallucinations and warping perceptions.



Causes of Alice in Wonderland Syndrome


This condition can be caused by different factors, which interfere with the way in which the brain communicates with the eyes. The signal receptors can be affected by things like intoxications with hallucinogens, migraine headaches, and tumours in the brain, headaches, and Epstein-Barr viral infection. In the initial stages of Epstein-Barr virus infection, a patient may hallucinate. This virus causes fever, swollen spleen, sore throat, and inflamed lymph nodes.


Epstein-Barr virus (EBV) is often a precursor to another condition known as mononucleosis.  Another cause associated with Alice in Wonderland Syndrome is temporal lobe epilepsy. If there is a seizure within the temporal lobes, it may lead to hallucinogenic symptoms. Use of psychoactive drugs can tripper Alice in Wonderland Syndrome. Some people experience the condition during the onset of their sleep.


What are the symptoms of Alice in Wonderland Syndrome?


If a person has this condition, there is altered perception on body images. This is the most common symptoms of Alice in Wonderland Syndrome. A person sees the sizes of the body parts disproportionately. A person may have a perceived disproportionate or incorrect size in head and hands. In addition, a person with the condition perceives incorrect size of other objects. The most disturbing symptoms are those related to alteration of body image.


A person with the condition may even be confused about his or her body size and shape.  Although the eyes are normal, a person sees objects in incorrect size and shape. For example, a person may see cars, people, and buildings in their incorrect size. These objects may appear larger or smaller. In the same way, distances may also look incorrect such as a corridor, which appears short instead of appearing long.










Migraine headache may be common with people suffering from Alice in Wonderland Syndrome. Moreover, there is loss of sense in time in which a person’s time may pass very slowly or it may seem to be passing very fast. To some extent, some patients may have hallucinations where they visualize things which are actually not there. Because of the hallucinations, patients may get wrong impressions on events, situations, or other things. Auditory and tactile perceptions are also affected. 



Alice in Wonderland Syndrome – Treatment


Although there is not any proven effective treatment, much of the treatment of Alice in Wonderland Syndrome may be directed to the symptoms. One way of managing the condition is by having plenty of rest. This is a common treatment for people with this condition. Other treatments for the condition are those similar for patients with migraines. 


Medications like antidepressants, anticonvulsants, beta-blockers and calcium channel blockers may be used in treating the condition. Moreover, there are alternative therapies applied to treat Alice in Wonderland Syndrome. If a patient is experiencing the condition due to effects caused by temporal lobe epilepsy, medications like topamax, neurontin, lamictal, and Phenobarbital are used to treat the epilepsy, which may in turn offer relieve of the symptoms of Alice in Wonderland Syndrome. 


To effectively tackle this condition, different treatment programs may be required depending on the probable cause. Besides the migraine medication such as antidepressants and beta blockers, a patient may be restricted to a migraine diet to help relieve the symptoms. Although a person with Alice in Wonderland Syndrome may experience hallucinations and distortions of images, these perceptions or manifestations may only last for a while and they subside. The hallucinations can occur numerous times during the day.


The problem with these distortions and hallucinations is that a patient become terrified and may be panic-stricken. Nonetheless, these distortions may not be dangerous or detrimental and will fade out with time. When a patient experiences such distortions during the day, resting may be the most effective way to get out the perceptions.


It is recommended that a patient joints support groups and communities in order to learn how to cope with the condition. Engaging in group discussions about the experiences people are going through from this condition can help bring hope and wellbeing to the person. A person is able to get support and a psychological understanding of the nature of the condition, something that can aid in tackling the Alice in Wonderland Syndrome better.












Rash Under Armpit

Rash Under Armpit
The armpit is one of the most sensitive parts of the body. It requires continuous care so as to prevent symptoms such as rashes. These rashes may appear because of using harmful deodorants and perfumes and they may also occur due to absence of regular cleaning. Even shaving the hair can lead to rashes if it is not done carefully. The important point here is to get the rashes treated as far as possible so that further damage can be prevented.










As mentioned before, rashes under armpits can appear due to applying deodorants to mask the small of sweat. The chemicals in the deodorant may trigger a reaction if the skin is too sensitive. People also need to be careful with the soaps that they are using since these products also contain chemicals.


Rashes under armpits can also appear due to clothes that are too tight or clothes that are made from synthetic materials. Clothes that wrap around the armpits tightly can lead to rashes. Hence it is always better to wear loose clothing that helps the free passage of air.


Rash under armpit can also occur if there is absence of proper hygiene. Sweat that accumulates under the armpit is susceptible to attracting bacteria which may trigger the rashes. In this case you can use a anti-bacterial soap and wash the armpits as directed.


Fungal infections are another cause for rashes. Ringworm is a common fungal infection which leads to itching and burning of the skin. If you develop an infection like this then you need to wash your armpits thoroughly and then let them dry. You can then apply an antifungal cream which clotimazole as one of the ingredients. If the problem persists or increases then you can call the doctor.










Rashes can also appear due to improver shaving. See to it that the razor is not very old and you shave the armpits slowly. Since old razors become dull you will need to use more force to remove the hair. Instead you can buy new razor and shave hair. Allergic reaction is another cause. This reaction can be triggered by certain fragrances, deodorants or soap. In this case, you can apply a special hydrocortisone cream.


Excessive heat us yet another cause. This normally leads to red bumps that are normally painless. They develop when the armpits are exposed to excessive heat and wetness. In this case, it is best to use talcum powder if the weather conditions persist. You can also apply topical corticosteroids to relieve the discomfort. If the armpits rub against each other, friction is caused and this can lead to rashes as well. Continuous friction leads to follicles being infected. Friction can happen when the clothes are too tight. The natural solution is to wear loose clothes.


Last but not the least are certain skin disorders such as dermatitis. In this case, skin infection can happen to any part of the body including the armpits. This problem can be solved by applying hydrocortisone or steroidal creams.


Underarm rash pictures
















PSA Blood Test – Normal Range, Low, High Levels

PSA Blood Test – Normal Range, Low, High Levels
PSA is also known as prostate specific antigen. This is a type of glycoprotein enzyme that is embedded in man by the KLK3 gene. This antigen is secreted by the epithelial cells in the prostate gland. PSA helps in ejaculating sperm as it changes the seminal coagulum into liquid form. This aids the sperm to flow and swim freely. PSA also plays a pivotal role in dissolving cervical mucus so that sperm can easily enter the mucus.










PSA is also found in limited quantities in men who have healthy prostates. However the levels are elevated in case of prostate cancer. It is better that the PSA levels are monitored periodically every 6 to 36 months and this period varies from case to case. These levels normally need to be monitored after treatment of prostate cancer.


In case surgery is successful to remove all prostate tissue, then PSA levels may become totally absent within a few weeks. However there could be a subsequent rise in level by 0.2 ng/dL and this may indicate residual benign prostate tissue or recurrent prostate cancer. In this case, further tests will show accurate results.



PSA levels may also be detected after radiation therapy for prostate cancer. This may be possible even when the treatment is complete. Hence it could be difficult to interpret the connection between the persistence of prostate cancer and PSA levels. The levels may also start decreasing after radiation therapy for several years. The lowest PSA level is also called nadir. However subsequent increase of PSA levels by 2.0 ng/dl above the nadir is acceptable.


High PSA levels that goes from 4 to 10 indicates 25 percent chances of prostate cancer, according to the information given by American Cancer Society. Elevated PSA levels which is more than 10 indicates 50 percent probability of prostate cancer.










If prostate cancer recurs after a rise in PSA levels and after treatment then it is known as biochemical recurrence. This recurrence could be due to various factors such as stage of cancer and PSA levels before treatment took place. The levels are normally low and 4 ng/mL is said to be fine. In case there are increased PSA levels then there are chances of prostate cancer. However cancer can also develop though there is no increase in PSA levels. Delayed detection of PSA levels may lead to advanced stages of prostate cancer. PSA levels can also increase due to other complications such as recent ejaculation, benign prostatic hyperplasia, irritation and prostatitis.


Normal PSA range


Given below is a table that recommends normal PSA levels for people in different age groups.


















































Age



<50



50 – 59



60 – 69



>70



(years)


CancerNo cancerCancerNo cancerCancerNo cancerCancerNo cancer
5th percentile0.40.31.20.31.70.32.30.4
(ng/mL)


95th percentile163.02.5372.54.7253.28.3613.217.8


Some of the factors that increase PSA levels include age, no ejaculation before 2 days of test, inflammation of the prostate gland and enlargement of the prostate which is not cancerous. Levels above 4 can indicate chances of suffering from prostate cancer. It is best to let the doctor know what medications you are taking before conducting the test. PSA levels need to need to be regularly monitored before and after prostate cancer treatment.












Scleroderma

Scleroderma
Scleroderma is a term used to refer to group of autoimmune disorders, which affects the connective tissue and skin. These diseases cause hardening and tightening of skin and other parts of the connective tissue or fibers providing framework and support for the body. Scleroderma may only affect the skin in some people but in others, it causes damages to other parts of the body besides the skin such as the internal organs, blood vessels, and digestive tract.










This condition is prevalent in women than in men and it manifests in ages of around 30 to 50 years. Scleroderma conditions are broadly grouped into two types, namely localized and generalized scleroderma. The localized scleroderma affects certain areas of the body. Morphea is a localized type of the condition, which involves oval shaped patches on the skin, which are hard. These patches start as purple or red spots, which then form a whitish center.


Linear localized scleroderma forms lines and streaks that have a thick skin and mainly affects the face, legs and arms. Of the generalized scleroderma conditions, there is limited and diffuse scleroderma. The limited scleroderma manifests gradually and affects the skin on face, feet and hands. It can advance to cause damage on organs like the lungs, intestines, and oesophagus. Diffuse scleroderma occurs more rapidly during its onset and affects the skin on trunk, upper arms and thighs. It can also affect internal organs like lungs, heart, and kidneys.


http://www.Symptoms-Causes-treatment.blogspot.com detect diseases at an early stage symptoms, and find out the causes and treatments best suited.

What are the causes of scleroderma?


It is not known what exactly causes scleroderma but scientists believe that the condition occurs due to an autoimmune response where the immune system begins to cause inflammation of skin and organs. The condition triggers the body to synthesize more collagen, a protein that gives the skin its structure. The result is a thickened and tightened skin as well as scarring internal organs.


Collagen forms the connective tissue fibrous network, which gives the structure of the organs including the skin, blood vessels, lungs, heart, and other organs. When the blood vessels are affected by abnormal spasm and thickening, they can result to damage of tissue and increased blood pressure within the pulmonary and systemic arteries.


What are the symptoms of scleroderma?


Symptoms can vary depending on the areas, which are affected. If the skin is affected, as happens to nearly all people with the condition, it hardens and thickens causing patches of oval shapes or straight lines. The skin also appears shiny since it is tight and has limited movement. An early sign of scleroderma is Raynaud’s phenomenon, which affects the fingers and toes causing abnormal reaction to cold temperatures and emotional distress. The toes may be numb, change their color, and become painful. The Raynaud’s phenomenon leads to red, blue, and white discoloration of the fingers and at times, it can cause ulceration.


Scleroderma can also affect the digestive system, whereby it causes an increase in acid that damages the esophagus near the stomach. There may be problems in absorption of nutrients through the intestinal wall because the intestine muscles may not be able to move food smoothly down the intestines. When the scleroderma affects organs like the lungs, heart, and kidneys, it can become life threatening though this happens rarely.










Scleroderma Treatment


Scleroderma affects many parts of the body something that can make it difficult to diagnose. Doctors may check if there are elevated levels of antibodies produced from the immune reaction. At times, scleroderma that affects the skin can subside and go away on its own. This may occur between three to five years since its onset. However, when internal organs are affected, they usually worsen over time.


There is no any drug that has been specifically developed to treat scleroderma and therefore most of the medications and therapies are aimed at treating its symptoms. In essence, there is no drug that can stop the overproduction of collagen, which causes the symptoms of scleroderma on the skin, blood vessels, and organs. Medications like blood vessel dilators may be used to counter increased blood pressure and prevent problems in organs like kidneys and lungs.


Medications to suppress the immune system may be used to reduce the reaction that causes the production of collagen. When ulceration occurs in the finger tips because of the Raynaud’s phenomenon, antibiotics may be used to prevent infections. Pain may be relieved with use of pain relievers. To manage the pain, nonsteroidal anti-inflammatory drugs- NSAIDs may be used to treat the inflammation. These include ibuprofen and aspirin.


Heartburn medication is recommended if the acid influx in the oesophagus is causing troubles. Physical and occupational therapy can be applied to manage pain, improve mobility, and strengthen the body. As a last resort, surgery may be used to treat complications of scleroderma such as damages of the lungs and blood vessels. Amputations may be done on fingers when severe Raynaud’s phenomenon causes ulcers that develop into gangrene. Organ transplant of the lungs may be performed if pulmonary hypertension damages of the lungs.


Scleroderma Pictures


















Turner Syndrome

Turner Syndrome
Turner syndrome is a condition associated with girl’s chromosomes where a girl grows short in height. When there is a problem with the girl’s X chromosome, it can lead to this condition. When diagnosed in advance, a girl can be treated for short stature and able to reach a height of about 1.4 meters or 4 feet and 7 inches. Researchers do not exactly know what causes Turner syndrome but they do hold that the condition occurs due to missing or incomplete X chromosomes. The X chromosomes are involved in body growth and sex development. This is the reason why girls with this condition tend to grow shorter and may have abnormal sexual features.










http://www.Symptoms-Causes-treatment.blogspot.com detect diseases at an early stage symptoms, and find out the causes and treatments best suited.

Causes of Turner Syndrome


Females have two X chromosomes, which they inherit from their parents. One X chromosome is inherited from the mother while the other X chromosome is passed from the father. When one of the X chromosomes is missing or incomplete, this may lead to Turner syndrome. A process known as nondisjunction may occur whereby the pair of sex chromosomes does not separate when eggs or sperms are forming.


An abnormal egg may bond with a normal sperm in the process of forming an embryo. In this situation, you have a person with an embryo, which misses one of the sex chromosomes referred to as X chromosome. Therefore, instead of having XX chromosomes, a girl may have only one X chromosome meaning one sex chromosome. When the embryo begins to grow, the cell division occurs but every cell has a missing X chromosomes.


Turner syndrome is not usually passed from affected parent to a child. This means that a mother may have Turner syndrome and not pass it to child. This is because in the first place, Turner syndrome leads to sterile condition in women where they cannot have children on their own without artificial fertilization.


In other cases, one of the two X chromosomes may be abnormal and result to growth problems in a girl. The reason why Turner syndrome is found in girls is because it involves the X chromosomes. By and large, female foetus with XX chromosomes can survive with one X chromosome but contrary to female foetus, male foetus, which is made up of XY chromosome, cannot survive without the X.


If a male foetus has only the Y chromosome and lacks the X chromosome, it will not survive. This again tries to explain why the condition is found in females than in males. Missing X chromosome is much worse than missing Y chromosome. To substantiate, Y chromosome contains fewer DNA molecules essential for life while X chromosome is a longer chain of DNA molecules with many genes that are responsible for cell functions in body.


Symptoms of Turner syndrome


Females with turner syndrome have problems with growth and sexual characters. Girls are shorter than normal. A woman with this condition has a stocky appearance and the arms may turn out at the elbow position. Another sign may be a receding lower jaw. A woman may also have a low hairline at the neck back and short webbed neck. In a webbed neck situation, there is development of extra skin folds, which extend from the shoulder tops to the neck sides. A girl may also have different shaped ears, which may be set in an unusual position at the lower sides of the head.


In addition, girls may also fail to start puberty when they attain the pubic age. This situation occurs because of underdevelopment of ovaries and synthesis of sex hormones like progesterone and oestrogen. When ovaries do not develop properly, it means that they cannot produce eggs and when this is coupled with problem in synthesis of sex hormones, it makes the puberty development a problem.










Besides these symptoms and signs, a girl may also show other symptoms such as swelling of hands and feet, in what is known as lymphedema. There may be heart and kidney defects, infertility and high blood pressure problems. Abnormal bone development may be witnessed in girls and particularly in the hands and arms. A girl may have more unusual moles on the skin. Because turner syndrome affects growth of body and sexual characteristics, a girl may experience self-esteem problems due to emotional challenges and self-denial.


Turner Syndrome Treatment


There is no specific cure for Turner syndrome because this condition is caused by abnormality in chromosomes. Nonetheless, there are treatments that can correct some of the problems and they are applied depending on the symptoms. People with Turner syndrome may show different symptoms. Some will have physical differences and body symptoms and others have fewer medical problems.


If the condition is diagnosed early in advance, a girl can lead near normal and healthy productive lifestyle. One form of treatment is use of growth hormone to improve the growth and development of the body. The growth hormones can influence the height of a girl, which is one of the aspects affected by the condition. The growth hormone treatment needs to be started early to aid the girl grow to average height range.


Moreover, oestrogen replacement may be done to help a girl reach and go through puberty stage. The oestrogen helps in enhancing physical changes of puberty such as menstrual periods and breast development. The oestrogen replacement treatment can be started at the age of 12 or 13.  Since Turner syndromes affects the ability of a women to become pregnant, doctors can use artificial ways of fertilisation to enable the women become pregnant.


A process known as “in vitro” fertilization is applied to help some women with the condition to bear children. A donor egg is used to create an embryo in a laboratory setting and then the embryo is introduced into the womb of the woman. With the right care, the woman can be able to carry the pregnancy and deliver a normal baby.


Other symptoms are managed such as lack of self-esteem and high blood pressure. Heart problems can be treated depending on their severity. Other conditions like thyroid problems may be addressed with use of hormones. Overweight, diabetes, hearing loss can also be treated with medications and changes in lifestyles. However, these are secondary symptoms and may not show in every other patient with the condition. Some girls may develop problems in their learning abilities and they need assistance in learning and in particular, mathematics.


Life expectancy in Turner Syndrome Patients


Women who have Turner Syndrome have a relatively lesser life expectancy compared to other healthier women.  The average age is 69-70 years with half of the patients dying from cardiovascular problems while 25 percent die from malignant issues.


Turner Syndrome Pictures including karyotype
















Low Grade Squamous Intraepithelial Lesion

Low Grade Squamous Intraepithelial Lesion
A low-grade squamous intraepithelial lesion is an abnormal growth of cells, which is thought to be just starting. It is the precancerous stage of the cancer of the cervix in which cancer may or may not develop. Squamous cells are part of the epithelial cells and they help in absorption, movement, and distribution of certain fluids and nutrients in body. When there is an abnormal growth of squamous cells at the cervix surface, it can cause what is known as squamous intraepithelial lesion.










The lower part of uterus is the one referred to as cervix. Cervix and uterus are found in the pelvis part of the body, which is close to top part of the ovaries and vagina. Cervix is the lower thin portion of uterus joining with the upper end of the vagina. There are mainly two types of cells in the cervix and they include the squamous epithelial cells and the columnar epithelial cells. The squamous epithelial cells form the lining of the outer part of cervix while columnar epithelial cells form the lining of the inner part of cervix.


Moreover, there are two types of squamous intraepithelial lesions or precancerous lesions and they include the low-grade and high-grade. Low-grade squamous intraepithelial lesions show a few changes in their size, number and shape. These cells have only a few abnormal characteristics and look similar to normal cells. When precancerous cells are detected in advance, they can be prevented from becoming cancerous.


Precancerous low-grade lesions are also referred to as mild dysplasia. These cells can advance and form high-grade squamous intraepithelial cells, which may look abnormal under the microscope. These high-grade lesions have not invaded deepest parts of cervix but they show a higher probability of suffering cervical cancer. They are referred to as severe dysplasia or carcinoma in situ, which implies the early stage of cancer.



http://www.Symptoms-Causes-treatment.blogspot.com detect diseases at an early stage symptoms, and find out the causes and treatments best suited.
  • 3 Treatment of low-grade squamous intraepithelial lesions

  • Causes of low grade squamous intraepithelial lesion


    In case of low-grade squamous intraepithelial lesions, the cells have not grown very abnormal and cervix has not been affected much. The low-grade squamous intraepithelial lesions are caused by things like infections, an injury or at times there may be no identifiable cause. When complications arise in the process of healing of an injury, it may result to low-grade squamous intraepithelial lesions. Sometimes, these changes in cells may go on their own.


    Almost all cases of cancer of the cervix are caused by oncogenic or high-risk infection mostly human papillomavirus, or HPV infections. The HPV infections are quite common but they can be suppressed by the body immune system without causing cancer. When infection of the cervix is caused by high-risk human papillomavirus, and it persists for some time, it can result to temporally changes in the cervix cells. Eventually the cells can develop to precancerous lesions. Without proper treatment, precancerous cells can progress to a cancer. It may take about 10 to 20 years or so to develop cancer from persist and serious infection with high-risk HPV.










    Diagnosis of low-grade squamous epithelial lesion


    A Pap smear or colposcopy is applied in testing for these low-grade squamous epithelial lesions. Pap smear is a testing procedure used to detect abnormal characteristics in cells. The specimen cells are scraped from the loose cells of the cervix and they are spread or smeared on a glass slide and examined under a microscope.


    Similarly, colposcopy entails visual examination of the cervix and vagina using magnifying equipment referred to as colposcope. The most effective way of diagnosing low-grade squamous intraepithelial lesion is through a biopsy with colposcopy equipment. In bioscopy examination, living tissue or cells are removed from part of the body being tested and then examined under a microscope or through a culture to help in diagnosing the problem. From the examination, a doctor can follow the course of disease or make an estimate on the progressive advancement of the cell abnormality changes.


    Low-grade squamous intraepithelial lesion and cervical cancer
    The presence of low-grade squamous intraepithelial lesions does not mean you have cancerous growth. When these cells are detected, it means that changes in the cells are occurring and they may precedent the occurrence of cancer. They are likely to occur before cancer starts growing. They may be regarded as warning signs of cervical cancer, which may occur at a later date.


    It is estimated that less than 1 percent of women who show positive test results for low-grade intraepithelial lesion using Pag smear are able to develop cervix cancer in the next two years. There is a marginally very low probability of developing cancer of the cervix when the results have shown presence of these abnormal changes in cells. Nonetheless, it is important to get treatment for the same to prevent any eventuality that may lead to a cancerous stage.


    Treatment of low-grade squamous intraepithelial lesions


    Although these abnormal changes in cells of the cervix may be noticed in a low grade-squamous intraepithelial lesion test, they may go away on their own without undergoing treatment. On the other hand, they can still develop to cancer stage when left untreated. If the condition is mild meaning the changes are fewer and mild, there is more likelihood that they will disappear on their own.


    But doctors at times do not want to take chances and may decide to remove them since there is possibility that they may advance to cancerous form. Treatment is done to remove or destroy the abnormal cells allowing new healthy cells to grow in the cervix. One technique used in destroying these cells is through use of below-freezing temperatures. Laser instruments may also be used to destroy them with a high frequency light beam.


    Electrical current or heat may be applied to destroy these cells. If the prevalence of the cells abnormality is higher, then the area or tissue affected may be removed. Freezing is normally used in small tissue areas and if the abnormality has affected larger areas, then this procedure may not be appropriate.


    For larger areas with changes in cells, laser or electrical current and heating may be more appropriate. Most of the abnormalities of the cells occur in the transformation zone that is located outside the cervix or in the canal of cervix. In this area, the cells are tall and shaped like a columnar and they are known as columnar cells. These columnar cells are transformed and changed into what is referred to as squamous cells.












    HbA1c – normal range, chart, blood test values

    HbA1c – normal range, chart, blood test values
    The Hemoglobin A1c normal range is referred to as the HbA1c normal range. Hemoglobin are the protein molecules which occur in the red blood cells present in the body. One of the key functions of hemoglobin is to supply the oxygen-rich blood from lungs to different tissues and organs in the body, and then take the carbon dioxide back to the lungs.










    All of us are aware that sugar has a sticky quality which makes it adhere to any kind of surface. Its elimination from that surface can also be quite arduous. The same rationality can be applied to the body. People with elevated levels of sugar in their bodies usually contain glycated hemoglobin in the bloodstream.


    The high sugar levels in the body trigger the excess sugar to bind itself to the hemoglobin, thereby leading to the formation of a coat of sugar on it. Red blood cells typically live for approximately 120 days in the bloodstream. This allows an HbA1c range test to determine the levels of sugar occurring in the body for over the past 3 months.


    As compared to regular monitoring of glucose carried out at home, an HbA1c range test is more reliable and relatively better.



    http://www.Symptoms-Causes-treatment.blogspot.com detect diseases at an early stage symptoms, and find out the causes and treatments best suited.

    The hemoglobin A1c normal range



    • A majority of HbA1c tests that are performed to ascertain the normal levels differ from one lab to the other.

    • Medical professionals maintain that the HbA1c normal range generally falls between four and six percent. A few other medical experts have stated that the HbA1c levels in diabetic patients should be below seven percent.

    • Since HbA1c range tests are used to ascertain the levels of blood sugar, it can act as a helpful tool to prevent the onset of different kinds of health complications that may arise due to an underlying presence of diabetes. An HbA1c test result which is higher than normal can warn patients to make changes in their lifestyle so as to prevent the development of related conditions and diseases like cardiac abnormalities, eye problems, kidney diseases, stroke, and nerve damage.

    • An HbA1c test result that is lower than normal often points to the present of a recent or current case of hypoglycemia. It is also a very serious situation, as low levels of blood sugar can result in death of the patient.

    • It may also be noted that test results indicating HbA1c readings as over 7 percent is a definite sign of poor maintenance and regulation of diabetes and blood sugar levels over the last few months. In these cases, patients may considerably reduce future instances of micro-vascular risks and complications by taking necessary steps to get the HbA1c levels back within the required normal range.


    It is thus safe to say that the HbA1c normal range test is one of the best methods to ascertain the levels of blood sugar in the body.


    HbA1c chart and levels of blood sugar


    The determination of HbA1clevels in the bloodstream is one of the first steps that a doctor will undertake to gauge the levels of blood sugar in the body.


    The HbA1ctest monitors the red blood cells to confirm the accumulation of sugar deposits on them during their lifespan, i.e. about 120 days. This allows a doctor to confirm whether or not the affected individual has followed the essential guidelines to keep the blood sugar levels under control over the last few weeks or months.It may be noted that a close correlation exists between the levels of blood sugar and the HbA1clevels. This allows a physician to recommend many easy-to-follow steps and lifestyle changes that can help a patient to effectively manage both the criteria.










    The table detailed below is an estimated measure of the correlation between the levels of blood sugar and HbA1c levels:

















































    HbA1c (%)  Average Blood Sugar (mg/dL)
    580
    6120
    7150
    8180
    9210
    10240
    11270
    12300
    13333
    14360


    The HbA1c normal range test



    • The values of HbA1c are found out via a blood test. A number of medical experts and professionals as well as different medical associations have confirmed the HbA1c test as the best method to diagnose the presence of diabetes.

    • An HbA1c test involves removal of a blood sample from the vein in an arm, which is then forwarded to labs for verifying the levels of HbA1c. If a person is diagnosed with diabetes, then the physician may recommend regular HbA1c tests in the future. Depending on the type of diabetes, the patient may need to undergo the HbA1c normal range test after every 3 to 6 months.

    • It is also important to note that individuals who have pre-existing medical disorders like kidney anomalies, liver conditions, and anemia; or have experienced heavy blood loss, may produce incorrect HbA1c test results with false numbers. An HbA1c test also comes with other risks such as buildup of blood below the skin, infection, dizziness, fainting, etc. which may be caused due to drawing of blood from the vein.

    • Patients have to remember the fact that varied labs offer varying HbA1c normal range test results. Hence, all HbA1c test results have to be checked by a physician for content and evaluation.


    It can however be positively concluded that the HbA1c normal range is one of the best ways to screen and manage the levels of blood sugar in the body. Regular visits to a doctor and monitoring can assist diabetic patients to continue a healthy diet and lifestyle.


    Treatment of abnormal blood sugar levels


    Treatment of diabetes includes oral medications, insulin injections, eating a balanced diet, and maintaining a healthy weight.



    • Your diet should consist of whole grains, vegetables, and fruits. Minimize the intake of animal products, sweets, and refined carbohydrates.

    • Exercise on a daily basis for at least 30 minutes a day

    • Patients affected by type 1 diabetes require insulin therapy for survival. A few type 2 diabetes patients may also need insulin therapy

    • Oral medications to stimulate insulin production by pancreas, or to inhibit release of glucose by liver are also given

    • Pancreas transplant and bariatric surgery are other treatment options.