CCFDN (medical condition): A rare, recessively inherited syndrome characterized by cataracts during infancy, unusual facial appearance and neuropathy.
See also:
CCFDN:
»Introduction: CCFDN
»Symptoms of CCFDN
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list CCFDN as a "rare disease".
Source - Orphanet
CCFDN (medical condition): See CCFDN (disease information).
»Introduction: CCFDN
»Symptoms of CCFDN
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