| congenital hemolytic a. |
1. hemolytic anemia that is present from birth and in which the lifespan of red blood cells is diminished, such as occurs in hereditary spherocytosis. 2. hereditary spherocytosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital hepatic f. |
a developmental disorder of the liver marked by formation of irregular broad bands of fibrous tissue containing multiple cysts formed by disordered terminal bile ducts, chiefly in the portal areas, resulting in vascular constriction, which leads to portal hypertension. It may be associated with polycystic renal disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital hypoplastic a. |
1. a progressive anemia of unknown etiology encountered in the first year of life, characterized by deficiency of red cell precursors in an otherwise normally cellular bone marrow; it is unresponsive to hematinics and often requires multiple blood transfusions. Called also Blackfan-Diamond a. or syndrome, Diamond-Blackfan a. or syndrome, congenital pure red cell a. or aplasia, congenital aregenerative a., and erythrogenesis imperfecta. 2. Fanconi syndrome (def. 1).
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital ichthyosiform e., bullous |
epidermolytic hyperkeratosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| congenital ichthyosiform e., nonbullous |
former name for lamellar ichthyosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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