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[Diagnosis and differential diagnosis of acute hepatic prophyrias (author's transl)].
MMW Munch Med Wochenschr. 1979 Nov 16; 121(46):1531-5.MM

Abstract

Diagnosis of porphyria is a clinical and biochemical procedure. Acute hepatic porphyrias are molecular regulation diseases which are characterized by a relative enzyme deficiency of the ferro-chelatase chain and an induction of hepatic delta-aminoacid synthase. There are indistinct clinical and pathobiochemical transitions between the three acute hepatic types of porphyria: acute intermittent porphyria, hereditary coproporphyria and porphyria variegata. They develop a similar acute clinical syndrome. The differential diagnosis is made possible by a differentiation of porphyrins and porphyrin precursers in the urine and the porphyrines in the stool and by the determination of uroporphyrinogen synthase activity in the erythrocytes.

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Pub Type(s)

English Abstract
Journal Article
Review

Language

ger

PubMed ID

117341

Citation

Doss, M. "[Diagnosis and Differential Diagnosis of Acute Hepatic Prophyrias (author's Transl)]." MMW, Munchener Medizinische Wochenschrift, vol. 121, no. 46, 1979, pp. 1531-5.
Doss M. [Diagnosis and differential diagnosis of acute hepatic prophyrias (author's transl)]. MMW Munch Med Wochenschr. 1979;121(46):1531-5.
Doss, M. (1979). [Diagnosis and differential diagnosis of acute hepatic prophyrias (author's transl)]. MMW, Munchener Medizinische Wochenschrift, 121(46), 1531-5.
Doss M. [Diagnosis and Differential Diagnosis of Acute Hepatic Prophyrias (author's Transl)]. MMW Munch Med Wochenschr. 1979 Nov 16;121(46):1531-5. PubMed PMID: 117341.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Diagnosis and differential diagnosis of acute hepatic prophyrias (author's transl)]. A1 - Doss,M, PY - 1979/11/16/pubmed PY - 1979/11/16/medline PY - 1979/11/16/entrez SP - 1531 EP - 5 JF - MMW, Munchener medizinische Wochenschrift JO - MMW Munch Med Wochenschr VL - 121 IS - 46 N2 - Diagnosis of porphyria is a clinical and biochemical procedure. Acute hepatic porphyrias are molecular regulation diseases which are characterized by a relative enzyme deficiency of the ferro-chelatase chain and an induction of hepatic delta-aminoacid synthase. There are indistinct clinical and pathobiochemical transitions between the three acute hepatic types of porphyria: acute intermittent porphyria, hereditary coproporphyria and porphyria variegata. They develop a similar acute clinical syndrome. The differential diagnosis is made possible by a differentiation of porphyrins and porphyrin precursers in the urine and the porphyrines in the stool and by the determination of uroporphyrinogen synthase activity in the erythrocytes. SN - 0341-3098 UR - https://www.unboundmedicine.com/medline/citation/117341/[Diagnosis_and_differential_diagnosis_of_acute_hepatic_prophyrias__author's_transl_]_ L2 - https://medlineplus.gov/porphyria.html DB - PRIME DP - Unbound Medicine ER -