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Prader Willi Syndrome
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Posted On :
Aug-18-2011
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Article Word Count :
428
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Prader Willi Syndrome (PWS), though an infrequent genetic problem, can affect both males and females of all races. Additionally it is known as 'chromosome 15 disorder'.
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Prader Willi Syndrome (PWS), though an infrequent genetic problem, can affect both males and females of all races. Additionally it is known as 'chromosome 15 disorder'.
Prader Willi Syndrome: Causes and Symptoms
Though it is known that the problem arises as a result of chromosomal abnormality; the main cause of such a genetic error still remains unknown. Scientists and researchers believe that genetic error or abnormality brought on during conception contributes to this disorder in babies. Second of all, severe injury to the some parts of the brain or the hypothalamus also can cause this condition. Additionally it is believed that this issue sometimes misses the parent, and can be found in the baby.
Nevertheless it should be noted that this problem is not handed down. Just about the most important point to note about Prader Willi syndrome signs or symptoms is that these symptoms are observed right from the fetal period. Reduced fetal movements, lethargy, sleepiness, difficulty in feeding, slower intellectual and physical growth, etc. are some of the symptoms of this disorder. Excessive extra weight and non-development of sexual organs (often leading to infertility) are the time-honored Prader-Willi syndrome signs. You could surely wonder is prader willi syndrome treatment available? Can the disorder be cured completely? Let us find strategies to these questions.
Diagnosis and Treatment:
Prader-Willi syndrome is diagnosed with assistance from distinctive physical characteristics and mental behavior/condition of the patient. The symptoms linked to this disorder can also help in diagnosis. Genetic testing (DNA-based methylation testing) is probably the techniques utilized to diagnose Prader-Willi syndrome.
Sadly, this syndrome has no cure. Nonetheless, earlier diagnosis of this disease in a newborn will help in availing treatments which will help lessen and control various effects of the syndrome. Newborns who are evident to carry this condition, once diagnosed with this problem, are given essential medication including growth hormones injection and treatments just like therapies to improve muscle tone, to reduce morbid obesity, educational therapies and speech related therapies etc. for other conditions connected with this syndrome.
Is Prader Willi syndrome cured / prevented?
Even though Prader Willi syndrome life span is rather good, unfortunately, this problem can't be cured. You'll be able to reduce the harshness of symptoms and live a normal life if proper treatment is followed. Simultaneously, because there is no known cause of the condition, there can't be any preventive steps. It should be also noted that just like this problem, the majority of the genetic disorders in children and adults can't be prevented.
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Article Source :
http://www.articleseen.com/Article_Prader Willi Syndrome_74745.aspx
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Author Resource :
Jacobybel Hyperthyroidism
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Keywords :
Prader Willi Syndrome, genetic error,
Category :
Disease And Illness
:
Disease And Illness
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