CCFDN - Genetics Home Reference - NIH - Congenital cataracts facial

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Congenital cataracts, facial dysmorphism, and neuropathy (CCFDN) is a rare disorder that affects several parts of the body. It is characterized by a clouding of​. Congenital cataracts, facial dysmorphism, and neuropathy (CCFDN) is characterized by abnormalities of the eye (bilateral congenital cataracts, microcornea, microphthalmia, micropupils); mildly dysmorphic facial features apparent in late childhood; and a hypo/demyelinating.

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Comments:

By Torr - 23:26
Congenital Cataracts Facial Dysmorphism Neuropathy (CCFDN) syndrome is a complex developmental disorder of autosomal recessive.
By Douzragore - 14:52
Congenital Cataracts Facial Dysmorphism Neuropathy (CCFDN) syndrome is a complex Developmental abnormalities include congenital cataracts and.
By Faegal - 16:24
Genetics Home Reference: Congenital cataracts, facial dysmorphism, and neuropathy (CCFDN) is a rare disorder that affects several parts of the body.
By Kajilabar - 20:18
Congenital cataracts, facial dysmorphism, and neuropathy is an autosomal recessive disorder that is prevalent among Bulgarian Gypsies. Additional features.
By Kazralar - 10:19
Congenital cataracts, facial dysmorphism, and neuropathy (CCFDN) syndrome is a rare autosomal recessive, complex developmental disorder exclusively.

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