Identification of a Novel Mutation in the SLC39A4 Gene in a Case of Acrodermatitis Enteropathica

Acta Derm Venereol. 2016 Mar;96(3):424-5. doi: 10.2340/00015555-2240.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Acrodermatitis / diagnosis
  • Acrodermatitis / drug therapy
  • Acrodermatitis / genetics*
  • Cation Transport Proteins / genetics*
  • DNA Mutational Analysis
  • Dietary Supplements
  • Female
  • Genetic Predisposition to Disease
  • Heterozygote
  • Humans
  • Infant
  • Mutation*
  • Phenotype
  • Skin / drug effects
  • Skin / pathology*
  • Treatment Outcome
  • Zinc / deficiency*

Substances

  • Cation Transport Proteins
  • SLC39A4 protein, human
  • Zinc

Supplementary concepts

  • Acrodermatitis enteropathica