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Mende syndrome: A rare condition characterized by congenital deafness, mutism, partial albinism and a mongoloid face as well as other anomalies. More detailed information about the symptoms, causes, and treatments of Mende syndrome is available below.
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Mende syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Mende syndrome, or a subtype of Mende syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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