Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex

Br J Dermatol. 2011 May;164(5):1113-6. doi: 10.1111/j.1365-2133.2011.10229.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Chromosomes, Human, Pair 13 / genetics*
  • Consanguinity
  • Hair / pathology*
  • Hair Diseases / congenital
  • Hair Diseases / genetics
  • Hair Diseases / pathology
  • Humans
  • Hypotrichosis / genetics
  • Hypotrichosis / pathology
  • Ichthyosis / genetics*
  • Ichthyosis / pathology
  • Male
  • Phenotype
  • Skin / pathology*
  • Young Adult

Supplementary concepts

  • Hypotrichosis simplex
  • Woolly hair, congenital