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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FAQs
How will my data be used?
Your data is yours. Which is why we have developed proprietary software linked to a dedicated platform, the Genome Manager, to provide you with unique access to your data whenever you want, wherever you are.
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You will be provided with a digital version of the raw data and reports. Thanks to these in-depth tools, you will be able to share your preferred information with your geneticist and/or doctor to indicate and plan the healthiest course for you.
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*Raw data will be available free of charge for the first 30 days after release.
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