Literature DB >> 25780817

Acrodermatitis Enteropathica: A Novel SLC39A4 Gene Mutation in a Patient with Normal Zinc Levels.

Verónica Garza-Rodríguez1, Alberto de la Fuente-García1, Carmen Liy-Wong1, Sébastien Küry2, Sébastien Schmitt2, Ijaz S Jamall3, Jorge Ocampo-Candiani1.   

Abstract

Acrodermatitis enteropathica (AE) is a rare disease that results from a defective gene, SLC39A4, and is characterized by dermatitis, alopecia, and diarrhea. We report a case of AE presenting with only periorificial and acral dermatitis in which genetic testing revealed two novel compound heterozygous missense mutations for SLC39A4. This case demonstrates that not all AE mutations alter zinc transporters in the same manner and highlights the phenotypic variability of AE.
© 2015 Wiley Periodicals, Inc.

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Year:  2015        PMID: 25780817     DOI: 10.1111/pde.12555

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  1 in total

1.  Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East.

Authors:  Faisel Abu-Duhier; Vivetha Pooranachandran; Andrew J G McDonagh; Andrew G Messenger; Johnathan Cooper-Knock; Youssef Bakri; Paul R Heath; Rachid Tazi-Ahnini
Journal:  Dermatol Res Pract       Date:  2018-08-07
  1 in total

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