Acquired erythropoietic uroporphyria secondary to myelodysplastic syndrome with chromosome 3 alterations: a case report-Reference-Cited by-同舟云学术

Acquired erythropoietic uroporphyria secondary to myelodysplastic syndrome with chromosome 3 alterations: a case report

Published:2018-03-02 Issue: Volume: Page:
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Podlipnik S.¹^ORCID,Guijarro F.²,Combalia A.¹^ORCID,To-Figueras J.³,Badenas C.³,Costa D.⁴,Rozman M.⁴,Jorge S.²,Aguilera P.¹,Gaya A.²

Affiliation:

1. Department of Dermatology; Hospital Clínic of Barcelona; University of Barcelona; Spain

2. Department of Haematology; Hospital Clínic of Barcelona; University of Barcelona; Spain

3. Department of Biochemistry and Molecular Genetics; Hospital Clínic of Barcelona; University of Barcelona; Spain

4. Department of Haematopathology; Hospital Clínic of Barcelona; University of Barcelona; Spain

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.15927/fullpdf

Reference13 articles.

1. Molecular genetics of congenital erythropoietic porphyria;Desnick;Semin Liver Dis,1998

2. Erwin A Balwani M Desnick R Porphyrias Consortium of the NIH-Sponsored Rare Diseases Clinical Research Network Congenital erythropoietic porphyria https://www.ncbi.nlm.nih.gov/books/NBK154652/

3. Congenital erythropoietic porphyria due to a mutation in GATA1: the first trans-acting mutation causative for a human porphyria;Phillips;Blood,2007

4. Congenital erythropoietic porphyria associated with myelodysplasia presenting in a 72-year-old man: report of a case and review of the literature;Kontos;Br J Dermatol,2003

5. Late onset erythropoietic porphyria;Horiguchi;Br J Dermatol,1989

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