| oculodentodigital d. |
a rare hereditary condition transmitted as an autosomal dominant trait, characterized by bilateral microphthalmos, abnormally small nose with anteverted nostrils, hypotrichosis, dental anomalies, camptodactyly, syndactyly, and missing phalanges of the toes. Called also dysplasia oculodentodigitalis syndrome, Meyer-Schwickerath and Weyers syndrome, oculodentodigital or oculodento-osseous syndrome, and ODD syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| oculodentodigital s. |
see under dysplasia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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