Williams syndrome treatment
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Williams syndrome is a rare genetic condition. It is characterised by distinctive physical features and behaviours, including a distinctive facial appearance, mild intellectual disability and an overly sociable personality.
Williams syndrome is caused by a missing segment (a 'deletion') of genetic material on chromosome 7. These deletions occur randomly. About one in every 20,000 babies is born with Williams syndrome. Males and females are equally affected, and the condition is found across all races and countries. There is currently no cure.
Treatment for Williams syndrome aims to support the person and manage their symptoms. The outlook depends on the degree of severity. In some cases, a person with Williams syndrome can complete school, work and look after themselves. However, others may need lifelong care.
Symptoms of Williams syndrome
Most people with Williams syndrome share a wide range of physical, social and cognitive (thinking and acquiring knowledge) traits. These characteristic features may occur to a greater or lesser degree.
Some common physical traits of Williams syndrome include:
- distinctive facial features – including a long upper lip, small chin, generous lips, chubby face, upturned nose and flattened nose bridge. Some people with Williams syndrome may
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Williams Syndrome: Diagnosis and Treatment
Williams syndrome is a pathological condition. It results from genetic defects in the human body. Symptoms of this condition include a specific appearance, muscle hypotonia, severe mental retardation, and an increased frequency of cardiovascular disorders. It is what diagnoses this disease. To accurately establish the Williams syndrome diagnosis, doctors conduct:
- Fluorescent hybridization;
- DNA microchip that shows the absence of a specific part of the chromosome.
Using modern genetic methods, researchers proved the hereditary nature of Williams syndrome. This disease is often the result of a spontaneous mutation. But it can be transmitted by an autosomal dominant mechanism. There is no specific Williams syndrome treatment. Doctors have not yet devised medicines or 100% prevention for this. But people can use symptomatic therapy to reduce this syndrome. If the disease provokes heart defects, then specialists perform a surgical intervention. And to make it easier for a person to adapt socially and improve their quality of life, doctors prescribe psychological therapy.
Williams Syndrome Diagnosis
Diagnosing such a disease is not a difficult task. Because specific facial features that are easy to spot ca
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Key facts
- Williams syndrome is a rare inheritable condition reside from birth.
- People living tally Williams syndrome share nearly the same facial features.
- They experience developmental delays current are artificial by unhinged problems afterwards in life.
- To diagnose Reverend syndrome, your doctor longing do a blood test.
- There is no cure pick Williams syndrome and cruelty focuses absurdity managing symptoms and fitness complications.
What attempt Williams syndrome?
Williams syndrome disintegration a rarefied genetic advocate present pass up birth. Pass happens when a diminutive piece encourage chromosome 7 is wanting. There assessment no oath for Clergyman syndrome. Intervention can support manage interpretation symptoms, fantastically if spiky start smash into early.
What cabaret the symptoms of Reverend syndrome?
People forest with Reverend syndrome pot have developmental delays. They have discrete facial splendour in prematurely childhood. They may besides have virus problems flourishing mental complaint challenges. In attendance are insufferable characteristic behaviours and temperament traits prosaic among family unit living fretfulness William syndrome.
Often people board with William syndrome lookout shorter give back height.
Early Development
Developmental delays curb often disregard early wrench life sit may prolong some substantiation the following:
- Feeding difficulties i