Literature DB >> 24131146

X-linked dominant protoporphyria: a new porphyria.

M J Seager1, S D Whatley, A V Anstey, T P Millard.   

Abstract

X-linked dominant protoporphyria (XLDPP) was first reported in the genetics literature in 2008. It has a phenotype very similar to erythropoietic protoporphyria (EPP), but is distinguished from EPP by higher concentrations of erythrocyte protoporphyrin (of which a high proportion is zinc-chelated), its apparently higher incidence of liver disease, and an X-linked dominant pattern of inheritance. Dermatologists should understand how XLDPP differs from EPP, in order to advise newly diagnosed patients correctly about the genetic implications and the long-term management strategy. We present a case series of XLDPP to introduce this condition to the dermatology literature.
© 2013 British Association of Dermatologists.

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Year:  2013        PMID: 24131146     DOI: 10.1111/ced.12202

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN: 0307-6938            Impact factor:   3.470


  2 in total

1.  X-chromosomal inactivation directly influences the phenotypic manifestation of X-linked protoporphyria.

Authors:  V Brancaleoni; M Balwani; F Granata; G Graziadei; P Missineo; V Fiorentino; S Fustinoni; M D Cappellini; H Naik; R J Desnick; E Di Pierro
Journal:  Clin Genet       Date:  2015-02-17       Impact factor: 4.438

2.  Educational Case: Rickets.

Authors:  Jonathan Light; Michele Retrouvey; Laurie L Wellman; Richard M Conran
Journal:  Acad Pathol       Date:  2022-09-23
  2 in total

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