| oral-facial-digital (OFD) s., type I |
a male-lethal X-linked dominant disorder characterized by camptodactyly, polydactyly, and syndactyly; by cranial, facial, lingual, and dental anomalies; and by mental retardation, familial trembling, alopecia, and seborrhea of the face and milia. Called also orodigitofacial dysostosis and orofaciodigital s., type I. See also Mohr s.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| oral-facial-digital (OFD) s., type II |
Mohr s.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| oral-facial-digital (OFD) s., type III |
an autosomal recessive disorder characterized by postaxial hexadactyly of the hands and feet, by ocular, lingual, and dental anomalies, and by profound mental retardation. Called also orodigitofacial dysostosis and orofaciodigital s., type III.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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