coproporphyria : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

coproporphyria	Presence of coproporphyrins in the urine, as in variegate porphyria. Hereditary coproporphyria, an inherited (autosomal dominant) disorder of a deficiency of coproporphyrinogen oxidase, resulting in overproduction of porphyrin precursors leading to neurological disturbances and photosensitivity. (05 Mar 2000)

CancerWEB 영영 의학사전 유사 검색 결과 : 1 페이지: 1

hereditary coproporphyria	<haematology> A group of metabolic disorders that result from a disturbance in porphyrin metabolism, causing increased formation and excretion of porphyrin or its precursors. Acute intermittent porphyria is a rare inherited form that can result in abdominal pain, photosensitivity and neurological disturbances. The various forms can be differentiated measuring various blood prophyrins. Inheritance: autosomal dominant. (27 Sep 1997)

hereditary coproporphyria

<haematology> A group of metabolic disorders that result from a disturbance in porphyrin metabolism, causing increased formation and excretion of porphyrin or its precursors.
Acute intermittent porphyria is a rare inherited form that can result in abdominal pain, photosensitivity and neurological disturbances. The various forms can be differentiated measuring various blood prophyrins.
Inheritance: autosomal dominant.
(27 Sep 1997)