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Patched mutations and hairy skin patches: a new sign in Gorlin syndrome

  • Louise C. Wilson
  • , Ekundayo Ajayi-Obe
  • , Birgitta Bernhard
  • , Saskia M. Maas

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

We report on the occurrence of discrete patches of unusually long pigmented hair on the skin of three patients with Gorlin syndrome from two unrelated families with confirmed heterozygous mutations in the Patched (PTCH) gene. The PTCH protein is a negative regulator of Hedgehog signaling, and the Sonic Hedgehog (SHH)-PTCH pathway is known to play an important role in the formation and cycling of the hair follicle. We believe that the patches represent a genuine physical sign associated with Gorlin syndrome, and discuss molecular mechanisms by which they might arise
Original languageEnglish
Pages (from-to)2625-2630
JournalAmerican journal of medical genetics. Part A
Volume140A
Issue number23
DOIs
Publication statusPublished - 2006

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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