Marie Unna hereditary hypotrichosis
MONDO:0018631A rare autosomal dominant hair loss disorder characterized by the absence or scarcity of scalp hair, eyebrows, and eyelashes at birth; coarse and wiry hair during childhood; and progressive hair loss beginning around puberty.
Also known as: HR hypotrichosis, MUHH, Marie Unna congenital hypotrichosis, hypotrichosis caused by mutation in HR, hypotrichosis, Marie Unna type
0 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.