| Literature DB >> 25780817 |
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.Entities:
Mesh:
Substances:
Year: 2015 PMID: 25780817 DOI: 10.1111/pde.12555
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588