Facioskeletalgenital syndrome, Rippberger type: A rare syndrome characterized by facial, skeletal and genital abnormalities. More detailed information about the symptoms, causes, and treatments of Facioskeletalgenital syndrome, Rippberger type is available below.
See full list of 26 symptoms of Facioskeletalgenital syndrome, Rippberger type
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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 Facioskeletalgenital syndrome, Rippberger type as a "rare disease".
Source - Orphanet
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