Want to learn exciting updates on the Edelife Clinical Trial, a potential prenatal treatment for boys affected by x-linked hypohidrotic ectodermal dysplasia (XLHED)? Download our library resource to watch this 45 minute webinar.
Genetic Variants
An ectodermal dysplasia is caused by a change(s) in a gene, called a variant. The NFED advocates that affected individuals work with a geneticist or genetics counselor to get genetic testing. Genetics can be very complex and you should always discuss your specific test with your genetics professional and direct your questions to them. In…
WNT10A Gene Causes Three Types of Ectodermal Dysplasia
WNT10A is a member of the WNT proteins family that is essential for the formation of tissues that arise from the ectoderm, including skin, hair, nails, teeth, and sweat glands. WNT10A is particularly important for the formation and shaping of both baby (primary) teeth and adult (permanent) teeth. Changes in the DNA) in WNT10A can…