![]() ![]() This means that most people with Williams syndrome have not inherited the condition from a parent. Williams syndrome usually occurs when someone is missing a small piece of chromosome 7. Williams syndrome can also cause endocrine concerns like having too much calcium in your blood and urine, an underactive thyroid and early puberty. Williams syndrome may cause poor growth in childhood, and most adults with the condition are shorter than average. Williams syndrome, also known as Williams-Beuren syndrome, is a rare, neurodevelopmental, genetic condition characterized by many symptoms including unique physical features, delayed development, cognitive challenges and cardiovascular abnormalities. Williams syndrome is a rare genetic condition that causes facial characteristics including epicanthal folds at the eyes, large ears, an upturned nose, full cheeks, a wide mouth, a small jaw and small teeth.
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