A Marie Unna Congenital Hypotrichosis anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Marie Unna Congenital Hypotrichosis. You're not alone.
Hello I am hoping to find someone who may have MUH. My daughter is just two years old and we have been trying to diagnose her coarse hair and sparse eyebrows. We are waiting for results of some genetic testing but according to some hair samples they believe it is MUH...