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alopecia universalis congenita

Epidemiology: rare Pathology: - hair loss characterized by hair follicles without hair Genetics: 1) autosomal recessive 2) associated with defects in hairless

Related

atrichia with papular lesions protein hairless; lysine-specific demethylase hairless (HR)

General

congenital anomaly (birth defect) genetic disease of the hair

References

  1. OMIM :accession 209500
  2. UniProt :accession O43593