Maarten and Linus were the first two boys treated before they were born with an investigational medicine for X-linked hypohidrotic ectodermal dysplasia. The boys are now 7 years old. The long-term results are incredibly positive! Read how they and the four other boys who were treated are doing.| National Foundation for Ectodermal Dysplasias
People with certain types of ectodermal dysplasia are not able to sweat normally. Because of this inability to sweat, people with this symptom need to be| National Foundation for Ectodermal Dysplasias
Guatemalan Family Fights to Save Their Baby| National Foundation for Ectodermal Dysplasias
Synonyms Anhidrotic ectodermal dysplasia Christ-Siemens-Touraine syndrome Forms X-linked hypohidrotic ectodermal dysplasia (XLHED) Autosomal recessive| National Foundation for Ectodermal Dysplasias
The EspeRare Foundation and Pierre Fabre Medicament seek to develop the first treatment for x-linked hypohidrotic ectodermal dysplasia (XLHED). They are| National Foundation for Ectodermal Dysplasias
