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Williams syndrome is a relatively rare multi‐system genetic syndrome caused by a chromosome 7q deletion. Each patient with GI concerns needs individualized evaluation based on their symptoms.
Most individuals with Williams syndrome experience GI issues at some point, especially abnormal bowel movement patterns (mainly constipation and related problems such as rectal prolapse & hemorrhoids) and bouts of abdominal pain.
1 Μαΐ 2008 · Signs & Symptoms. Williams syndrome is characterized by a wide spectrum of symptoms and physical features that vary greatly in range and severity, even among affected family members. Individuals with Williams syndrome will not have all the symptoms listed below.
To celebrate the 40th anniversary of the Williams Syndrome Foundation and to raise awareness of Williams syndrome, we have put together 40 research-evidenced facts about Williams syndrome. Williams Syndrome is a rare genetic condition that is caused by a deletion of genetic material on the long arm of chromosome 7.
22 Οκτ 2024 · This article will explore the prevalence, causes, signs and symptoms, diagnosis, treatment, and latest research on Williams Syndrome. Causes of Williams Syndrome. Large gene deletions from a specific band on the long arm of chromosome 7 cause Williams Syndrome.
22 Σεπ 2024 · Some common signs of Williams syndrome include: Unique personality; Unique facial features; Chronic ear issues; Being very sensitive to sound; Heart problems; Attention deficit hyperactivity...
PHYSICAL AND MEDICAL FEATURES OF WILLIAMS SYNDROME IN ADULTHOOD. Individuals with WS are often of short stature: the average adult height is 5ft for females and 5ft 6in for males. Although many children with WS are of slight build, there is a tendency for some individuals to put on weight, as they get older.
