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[The porphyria cutanea tarda group: their role among the enzyme defects of heme biosynthesis].
Sem Hop 1984; 60(16):1148-52SH

Abstract

Porphyria cutanea tarda (PCT) is the most common porphyria. In contrast to the other porphyrias, which are undisputably hereditary, PCT was long considered to be acquired. However, the recent demonstration of a defect in uroporphyrinogen decarboxylase suggests that PCT is supported by a genetic factor. Though the hereditary or acquired nature of the enzymatic defect is still under debate, it seems that the disease has a polygenic origin involving an impairment of iron metabolism and a specific genetic background.

Authors

No affiliation info availableNo affiliation info available

Pub Type(s)

English Abstract
Journal Article

Language

fre

PubMed ID

6326308

Citation

Adrien, A, and G Guillet. "[The Porphyria Cutanea Tarda Group: Their Role Among the Enzyme Defects of Heme Biosynthesis]." La Semaine Des Hopitaux : Organe Fonde Par l'Association D'enseignement Medical Des Hopitaux De Paris, vol. 60, no. 16, 1984, pp. 1148-52.
Adrien A, Guillet G. [The porphyria cutanea tarda group: their role among the enzyme defects of heme biosynthesis]. Sem Hop. 1984;60(16):1148-52.
Adrien, A., & Guillet, G. (1984). [The porphyria cutanea tarda group: their role among the enzyme defects of heme biosynthesis]. La Semaine Des Hopitaux : Organe Fonde Par l'Association D'enseignement Medical Des Hopitaux De Paris, 60(16), pp. 1148-52.
Adrien A, Guillet G. [The Porphyria Cutanea Tarda Group: Their Role Among the Enzyme Defects of Heme Biosynthesis]. Sem Hop. 1984 Apr 12;60(16):1148-52. PubMed PMID: 6326308.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [The porphyria cutanea tarda group: their role among the enzyme defects of heme biosynthesis]. AU - Adrien,A, AU - Guillet,G, PY - 1984/4/12/pubmed PY - 1984/4/12/medline PY - 1984/4/12/entrez SP - 1148 EP - 52 JF - La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris JO - Sem Hop VL - 60 IS - 16 N2 - Porphyria cutanea tarda (PCT) is the most common porphyria. In contrast to the other porphyrias, which are undisputably hereditary, PCT was long considered to be acquired. However, the recent demonstration of a defect in uroporphyrinogen decarboxylase suggests that PCT is supported by a genetic factor. Though the hereditary or acquired nature of the enzymatic defect is still under debate, it seems that the disease has a polygenic origin involving an impairment of iron metabolism and a specific genetic background. UR - https://www.unboundmedicine.com/medline/citation/6326308/[The_porphyria_cutanea_tarda_group:_their_role_among_the_enzyme_defects_of_heme_biosynthesis]_ L2 - http://www.diseaseinfosearch.org/result/5879 DB - PRIME DP - Unbound Medicine ER -