| congenital d. of the hip |
developmental dysplasia of the hip.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital dyserythropoietic a. |
any of several rare hereditary anemias, mostly types of macrocytic anemia, characterized by nuclear anomalies of the erythrocytes, such as multinuclearity, karyorrhexis, or macrocytosis. The most common type (called also HEMPAS) is an autosomal recessive condition characterized by multinuclear erythrocytes and a positive acidified serum test.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital e. |
Milroy disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital ectodermal d. |
anhidrotic ectodermal dysplasia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital erythropoietic p. |
an autosomal recessive porphyria in which increased synthesis of uroporphyrinogen I relative to uroporphyrinogen III occurs in bone marrow erythroblasts; it is characterized by cutaneous photosensitivity, leading to mutilating skin lesions, by hemolytic anemia and splenomegaly, and by greatly increased urinary excretion of uroporphyrin I and coproporphyrin I. Erythrodontia and hypertrichosis are invariably present. It appears to be due to deficiency of uroporphyrinogen-III synthase. Called also congenital photosensitive p., Günther disease, and erythropoietic uroporphyria.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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