Marie Unna hereditary hypotrichosis

MONDO:0018631

A 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 trials

Sub-types

Broader categories

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.