Acrodermatitis Enteropathica Report

Dhs. 118.00

Acrodermatitis Enteropathica

Acrodermatitis Enteropathica is a rare congenital form of zinc deficiency, which occurs in the first weeks of life, in bottle-fed children or at the time of weaning. Caused by mutations in genes responsible for zinc metabolism, AE manifests with ocular, skin and gastrointestinal symptoms, but is manageable with lifelong zinc supplements.

2 genes analyzed


It is recommended if:

This report is particularly suitable for infants who, in the first weeks of life, show gastrointestinal, skin and ocular symptoms compatible with Acrodermatitis enteropatica.


List of main conditions:

  • Zinc deficiency, transient neonatal
  • Acrodermatitis enteropathica
  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • Investigates SNP and Indel mutations up to 150 bp

Simple workflow

*To generate this report, a sequencing test is mandatory. If you have not yet acquired a sequencing test, kindly make the purchase at this link: Dante Genome Test now!

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