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hypotrichosis simplex of scalp (Spanish type)
Genetics:
1) autosomal dominant
2) associated with defects in CDSN gene
Clinical manifestations:
- isoloated alopecia
- affected individuals have normal hair in early childhood
- progressive loss of scalp hair beginning in the middle of the 1st decade
- almost complete baldness by the 3rd decade of life
General
hypotrichosis
scalp disorder
Database Correlations
OMIM 146520
References
OMIM :accession 146520