ORPHA:444
Marie Unna hereditary hypotrichosis
Also called Hypotrichosis, Marie Unna type, MUHH, Marie Unna congenital hypotrichosis
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:444 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Alopecia
- Coarse hair
- Sparse scalp hair
- Aplasia/Hypoplasia of the eyebrow
- Sparse or absent eyelashes