Literature DB >> 22082465

Novel SLC39A4 mutation in acrodermatitis enteropathica.

Alexandra Coromilas1, Heather A Brandling-Bennett, Kimberly D Morel, Wendy K Chung.   

Abstract

Acrodermatitis enteropathica (AE) is a rare autosomal-recessive disorder characterized by dermatitis, alopecia, diarrhea, and retardation of growth and development. AE maps to 8q24.3 and is associated with mutations in the intestinal zinc transporter ZIP4 encoded by the gene SLC39A4. We describe a novel homozygous mutation, 1191insC, in SLC39A4 in a patient from Sierra Leone and suggest that AE should be considered within the differential diagnosis for acrodermatitis in children from Sierra Leone. Genetic testing for this founder mutation can be easily performed for this treatable disorder.
© 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 22082465     DOI: 10.1111/j.1525-1470.2011.01637.x

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


  2 in total

1.  Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature.

Authors:  G Ricci; S Ferrari; E Calamelli; L Ricci; I Neri; A Patrizi
Journal:  Int J Immunopathol Pharmacol       Date:  2015-12-18       Impact factor: 3.219

2.  Molecular Basis of Transient Neonatal Zinc Deficiency: NOVEL ZnT2 MUTATIONS DISRUPTING ZINC BINDING AND PERMEATION.

Authors:  Yarden Golan; Naoya Itsumura; Fabian Glaser; Bluma Berman; Taiho Kambe; Yehuda G Assaraf
Journal:  J Biol Chem       Date:  2016-05-02       Impact factor: 5.157

  2 in total

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