Pena-Shokeir syndrome Type 2: A rare progressive congenital syndrome involving degeneration of the brain and spinal cord and characterized by facial, head, skeletal and muscular abnormalities as well as eye abnormalities. More detailed information about the symptoms, causes, and treatments of Pena-Shokeir syndrome Type 2 is available below.
See full list of 38 symptoms of Pena-Shokeir syndrome Type 2
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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 Pena-Shokeir syndrome Type 2 as a "rare disease".
Source - Orphanet
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