Ectodermal Dysplasias Report
Ectodermal dysplasias
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.
24 genes analyzed
It is recommended if:
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.
List of main conditions:
- Ectodermal dysplasia 1, hypohidrotic, X-linked
- Ectodermal dysplasia 10A/10B
- Ectodermal dysplasia 11A/11B
- Congenital heart defects and ectodermal dysplasia
Simple workflow
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*Raw data will be available free of charge for the first 30 days after release.
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