Weismann-Netter-Stuhl Syndrome: A very rare inherited disorder characterized by bone development abnormalities. More detailed information about the symptoms, causes, and treatments of Weismann-Netter-Stuhl Syndrome is available below.
See full list of 12 symptoms of Weismann-Netter-Stuhl Syndrome
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Types of Weismann-Netter-Stuhl Syndrome
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Weismann-Netter-Stuhl Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Weismann-Netter-Stuhl Syndrome, or a subtype of Weismann-Netter-Stuhl Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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