Acrodermatitis enteropathica and an overview of zinc metabolism

J Am Acad Dermatol. 2007 Jan;56(1):116-24. doi: 10.1016/j.jaad.2006.08.015. Epub 2006 Oct 30.

Abstract

Acrodermatitis enteropathica is a rare autosomal recessive disorder of zinc deficiency. The genetic defect has been mapped to 8q24 and the defective gene identified as SLC39A4, which encodes the zinc transporter Zip4. The diagnosis is made by way of clinical presentation together with histopathology and laboratory tests. Here we provide an overview of zinc metabolism and a description of inherited and acquired zinc deficiency.

Publication types

  • Review

MeSH terms

  • Acrodermatitis / diagnosis
  • Acrodermatitis / epidemiology
  • Acrodermatitis / genetics*
  • Acrodermatitis / metabolism
  • Adult
  • Animals
  • Cation Transport Proteins / chemistry
  • Cation Transport Proteins / deficiency*
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / physiology
  • Diet
  • Disease Models, Animal
  • Female
  • Gene Expression Regulation
  • Genes, Recessive
  • Humans
  • Infant
  • Intestinal Absorption
  • Intestinal Mucosa / metabolism
  • Jejunum / metabolism
  • Malabsorption Syndromes / diagnosis
  • Malabsorption Syndromes / epidemiology
  • Malabsorption Syndromes / genetics*
  • Malabsorption Syndromes / metabolism
  • Male
  • Mice
  • Mice, Mutant Strains
  • Milk / chemistry
  • Nutritional Requirements
  • Skin / pathology
  • Zinc / deficiency*
  • Zinc / metabolism
  • Zinc / pharmacokinetics
  • Zinc / physiology
  • Zinc / therapeutic use

Substances

  • Cation Transport Proteins
  • SLC39A4 protein, human
  • Zinc