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chloroquine and Coproporphyria, Hereditary

chloroquine has been researched along with Coproporphyria, Hereditary in 1 studies

Chloroquine: The prototypical antimalarial agent with a mechanism that is not well understood. It has also been used to treat rheumatoid arthritis, systemic lupus erythematosus, and in the systemic therapy of amebic liver abscesses.
chloroquine : An aminoquinoline that is quinoline which is substituted at position 4 by a [5-(diethylamino)pentan-2-yl]amino group at at position 7 by chlorine. It is used for the treatment of malaria, hepatic amoebiasis, lupus erythematosus, light-sensitive skin eruptions, and rheumatoid arthritis.

Coproporphyria, Hereditary: An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, 5-AMINOLEVULINATE and COPROPORPHYRINS.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
DAVIS, MJ1
PLOEG, DE1

Other Studies

1 other study available for chloroquine and Coproporphyria, Hereditary

ArticleYear
Acute porphyria and coproporphyrinuria following chloroquine therapy; a report of two cases.
    A.M.A. archives of dermatology, 1957, Volume: 75, Issue:6

    Topics: Chloroquine; Coproporphyria, Hereditary; Humans; Porphyria, Acute Intermittent; Porphyrias; Porphyri

1957