Causes. Williams syndrome is caused by the loss (deletion ) of genetic material from a specific region of chromosome 7 . The deleted region includes 25 to 27 genes, and researchers believe that a loss of several of these genes contributes to the characteristic features of this disorder.
31 мая 2022 г.
Williams syndrome is a rare genetic disorder with congenital heart disease, distinctive facial features (elfin-like faces), hypercalcemia, neurodevelopmental, ... |
7 авг. 2024 г. · Williams syndrome is a rare genetic condition affecting multiple organ systems. Originally described independently by Williams and Beuren in ... |
13 апр. 2023 г. · Williams syndrome (WS) is characterized by developmental delay, intellectual disability (usually mild), a specific cognitive profile, unique personality ... |
The syndrome is characterized by cognitive and behavioral abnormalities that include mild to moderate mental retardation, delayed language and motor development ... |
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 ... What causes Williams... · Diagnosis of Williams syndrome |
Learn about Williams Syndrome, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find ... |
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