Ectodermal Dysplasias Panel

This product is only meant for customers who already purchased a Dante Genome Test

Ectodermal dysplasias (ED) are a group of rare disorders in which abnormalities occur in the skin, hair, teeth, nails and sweat glands. There are several types and the clinical picture is variable, also depending on the gene involved. Hypohidrotic ectodermal dysplasia (HED) is the most common type. Currently, there is no cure for HED, however, treatment is based on symptom management and care of affected people.
This test is indicated for those who have a personal or family history of ectodermal dysplasia, or present with symptoms such as abnormalities of the fingernails and toenails, dental abnormalities, reduced sweating and lack of scalp or body hair.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • 24 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Ectodermal dysplasia 1, hypohidrotic, X-linked
  • Ectodermal dysplasia 10A/10B
  • Ectodermal dysplasia 11A/11B
  • Congenital heart defects and ectodermal dysplasia

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