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Beare-Stevenson cutis gyrata syndrome: A rare genetic disorder involving skin and skull abnormalities due to the premature fusion of skull bones. More detailed information about the symptoms, causes, and treatments of Beare-Stevenson cutis gyrata syndrome is available below.
See full list of 13 symptoms of Beare-Stevenson cutis gyrata syndrome
Read more about complications of Beare-Stevenson cutis gyrata syndrome.
Research the causes of these diseases that are similar to, or related to, Beare-Stevenson cutis gyrata syndrome:
Medical news articles related to Beare-Stevenson cutis gyrata syndrome include:
Source: HealthDay News
Medical research articles related to Beare-Stevenson cutis gyrata syndrome include:
Click here to find more evidence-based articles on the TRIP Database
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Visit our research pages for current research about Beare-Stevenson cutis gyrata syndrome treatments.
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Twisted hair, sparsity of body hair, and fragile nails, and mental retardation. - (Source - Diseases Database)
Beare-Stevenson cutis gyrata syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Beare-Stevenson cutis gyrata syndrome, or a subtype of Beare-Stevenson cutis gyrata syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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