Ampola syndrome: A rare genetic disease characterized primarily by mental retardation, facial anomalies, short stature, seizures and finger and toe abnormalities. More detailed information about the symptoms, causes, and treatments of Ampola syndrome is available below.
See full list of 49 symptoms of Ampola syndrome
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Ampola syndrome as a "rare disease".
Source - Orphanet
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