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alopecia universalis congenita Mari type
Epidemiology:
- common in the Mari population, a large aboriginal Finno-Ugric population in the Volga-Ural region of Russia
Genetics:
- autosomal recessive
- associated with defects in LIPH gene
Clinical manifestations:
- congenital hypotrichosis of scalp hairs
- any hair present being wiry & twisted
General
alopecia (hair loss, balding)
genetic disease of the hair
Database Correlations
OMIM 604379
References
OMIM :accession 604379