Literature DB >> 7398998

Two cases in infantile and familial porphyria cutanea tarda.

M J Cruces Prado, R Enriquez de Salamanca, M Verea Hernando, M L Peña Payero, T Catalán Beltran, A Robledo Aguilar.   

Abstract

In 2 children, both 7 years old, and with an obvious presence of clinical symptoms, the diagnosis of porphyria cutanea tarda was corroborated by the characteristic patterns of urinary and fecal prophyrin excretion. Familial studies allowed us to consider both cases as hereditary.

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Year:  1980        PMID: 7398998     DOI: 10.1159/000250359

Source DB:  PubMed          Journal:  Dermatologica        ISSN: 0011-9075


  3 in total

1.  Porphyria cutanea tarda and beta-thalassaemia minor with iron overload.

Authors:  R S Day; P B Disler; L Eales
Journal:  Br Med J       Date:  1980-09-20

2.  Uroporphyrinogen decarboxylase: complete human gene sequence and molecular study of three families with hepatoerythropoietic porphyria.

Authors:  M J Moran-Jimenez; C Ged; M Romana; R Enriquez De Salamanca; A Taïeb; G Topi; L D'Alessandro; H de Verneuil
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

3.  Hepatoerythropoietic porphyria precipitated by viral hepatitis.

Authors:  R J Hift; P N Meissner; G Todd
Journal:  Gut       Date:  1993-11       Impact factor: 23.059

  3 in total

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