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General
Williams syndrome is a rare genetic condition characterized by unique physical features, neurodevelopmental issues, cognitive difficulties and cardiovascular abnormalities. Williams syndrome is caused due to a missing piece of the 7th chromosome, and is usually not inherited from the parents.
9 people with Williams syndrome are on Alike.
"Alike is the place to get answers from people who firsthand share your health challenges"
Signs & symptoms
Symptoms may include ear infection, hearing loss, dental abnormalities, elevated calcium levels in the blood, hypothyroidism, early puberty, diabetes, farsightedness, feeding difficulties, scoliosis, sleep problems, and short stature.
Diagnosis
Diagnosis is based upon findings from medical history and physical examination. Further evaluation may include genetic tests.
Treatment
Treatment depends on the specific symptoms and difficulties.
Note
☝ We provide information on prescription and over-the-counter medicines, diagnosis, procedures and lab tests. This material is provided for educational purposes only and is not medical advice, diagnosis or treatment.
National Institutes of Health ∙ World Health Organization ∙ MedlinePluse ∙ Centers for Disease Control and Prevention
☝ All information has been reviewed by certified physicians from Alike
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