| 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...
|
|---|---|
| oculodentodigital s. |
see under dysplasia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| oculodermal m. |
nevus of Ota.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| oculofacial |
pertaining to the eyes and the face.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| oculoglandular t. |
a form of tularemia in which the primary site of entry of Francisella tularensis is the conjunctival sac, characterized by conjunctivitis, itching, lacrimation, pain, granulomatous corneal lesions that if untreated may result in perforation of the cornea and optic atrophy, and enlargement of preauricular lymph nodes.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|