Orstavik-Lindemann-Solberg syndrome: A rare disorder characterized by congenital heart defects, tongue tumors, extra fingers and webbing of fingers. More detailed information about the symptoms, causes, and treatments of Orstavik-Lindemann-Solberg syndrome is available below.
See full list of 9 symptoms of Orstavik-Lindemann-Solberg syndrome
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Read more about causes of Orstavik-Lindemann-Solberg syndrome.
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Read more about Misdiagnosis and Orstavik-Lindemann-Solberg syndrome
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Orstavik-Lindemann-Solberg syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Orstavik-Lindemann-Solberg syndrome, or a subtype of Orstavik-Lindemann-Solberg syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Orstavik-Lindemann-Solberg syndrome as a "rare disease".
Source - Orphanet
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