William Syndrom Symptomer
The condition is typically diagnosed in infancy or early childhood. Williams syndrome is inherited and sometimes spontaneous.
Hva Er Williams Syndrom Sjelden
Symptoms of williams syndrome can be treated but there is no cure.
William syndrom symptomer. It causes many developmental problems. A syndrome is a medical condition that shows a specific set of symptoms together. People with williams syndrome have a 50 chance of passing the condition on to each of their offspring. Children with this syndrome could have problems with their heart blood vessels kidneys and. What are the symptoms of williams syndrome. Your doctor may note symptoms over time and carry out the diagnosis. The deleted region includes more than 25 genes and researchers believe that being hemizygous for these genes probably contributes to the characteristic features of this syndrome. Not all people with williams syndrome will have the same. Accordingly the deletion is present at the time of conception. Williams syndrome is a microdeletion syndrome caused by the spontaneous deletion of genetic material from the region q1123 of one member of the pair of chromosome 7 so that the person is hemizygous for those genes. The deletion occurs in either the egg or the sperm used to form the child with williams syndrome. Williams syndrome is a rare genetic disorder with characteristic features signs and symptoms like digestive and eye problems low birth weight and cardiac abnormalities. Genetic causes treatments and life expectancy information are provided. This syndrome affects the facial features of sufferers to cause what is called an elfin appearance in individuals. Williams syndrome also called williams beuren syndrome is a rare genetic disorder.
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