Santos-Mateus-Leal syndrome: A very rare syndrome characterized mainly by extra fingers, deafness and an intestinal disorder called Hirschsprung disease where waste material fails to move effectively through the intestinal system resulting in constipation. More detailed information about the symptoms, causes, and treatments of Santos-Mateus-Leal syndrome is available below.
See full list of 8 symptoms of Santos-Mateus-Leal syndrome
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Read more about Misdiagnosis and Santos-Mateus-Leal syndrome
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Santos-Mateus-Leal syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Santos-Mateus-Leal syndrome, or a subtype of Santos-Mateus-Leal 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 Santos-Mateus-Leal syndrome as a "rare disease".
Source - Orphanet
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