Hereditary Coproporphyria

Known as: CPO DEFICIENCY, hereditary coproporphyria porphyria, Coproporphyrinogen Oxidase Deficiency 
An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1954-2017
051019542016

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2005
2005
Hereditary coproporphyria is an autosomal dominant disorder resulting from the half-normal activity of coproporphyrinogen oxidase… (More)
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1999
1999
Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by deficient activity of… (More)
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1994
1994
Coproporphyrinogen oxidase is a mitochondrial heme-biosynthetic enzyme that converts coproporphyrinogen to protoporphyrinogen… (More)
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1994
1994
A 23-year-old man with epilepsy and a past history of abdominal pain and ileus, developed hypertension and arm and bulbar… (More)
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1992
1992
To see whether the fecal coproporphyrin III:coproporphyrin I (CIII:CI) ratio (determined by HPLC) would be suitable for screening… (More)
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1990
1990
Seizures are common in acute exacerbations of hepatic porphyria, even though the etiology is not identified in most cases. We… (More)
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1984
1984
In a family inheriting the hereditary coproporphyria (HCP) gene, where 414 descendants have been traced through six generations… (More)
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1983
1983
Three siblings with intense jaundice and hemolytic anemia at birth were found to excrete a high level of coproporphyrin in their… (More)
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1977
1977
A 9-year-old boy with mental deterioration and epilepsy suffered an acute attack of hereditary coproporphyria associated with… (More)
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1976
1976
The activity of coproporphyrinogen oxidase (E.C. 1.3.3.3) in cultured skin fibroblasts from three patients with hereditary… (More)
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