[Hereditary zinc deficiency]

Tidsskr Nor Laegeforen. 2015 Mar 10;135(5):440. doi: 10.4045/tidsskr.14.1548.
[Article in Norwegian]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Acrodermatitis* / genetics
  • Acrodermatitis* / pathology
  • Cation Transport Proteins / genetics
  • Humans
  • Infant
  • Male
  • Zinc / deficiency*

Substances

  • Cation Transport Proteins
  • SLC39A4 protein, human
  • Zinc

Supplementary concepts

  • Acrodermatitis enteropathica