Format

Send to:

Choose Destination
See comment in PubMed Commons below
Cutis. 2009 Nov;84(5):269-71.

Pachyonychia congenita: a case report.

Author information

  • 1Kinser Medical Branch Clinic, Okinawa, Japan, nkohli@mednet.ucla.edu

Abstract

A 21-year-old man presented with hypertrophic nail dystrophy and subungual debris of all 20 nails, hyperkeratotic plaques on the heels of both feet, and oral leukokeratosis. He had an extensive family history of similar clinical findings. The patient's clinical presentation and history were consistent with pachyonychia congenita (PC), an autosomal dominant genodermatosis caused by mutations in the genes for keratin 6, K6a and K6b; keratin 16, K16; and keratin 17, K17.

PMID:
20099620
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Loading ...
    Write to the Help Desk