Nail dystrophy, an unusual presentation of incontinentia pigmenti

Br J Dermatol. 2003 Dec;149(6):1286-8. doi: 10.1111/j.1365-2133.2003.05694.x.

Abstract

We describe a 57-year-old woman with a history of nail dystrophy since the age of 11 years. Multiple nail clippings were negative and multiple empirical treatments for presumed onychomycosis were unsuccessful. The patient has a daughter with classical incontinentia pigmenti. Molecular genetic analysis was positive for the NEMO gene deletion on the X chromosome, confirming the diagnosis of incontinentia pigmenti. Nail dystrophy was the sole feature of the disease in our patient.

Publication types

  • Case Reports

MeSH terms

  • Chromosomes, Human, X
  • Female
  • Gene Deletion
  • Humans
  • I-kappa B Kinase
  • Incontinentia Pigmenti / complications*
  • Incontinentia Pigmenti / genetics
  • Middle Aged
  • Nails, Malformed / etiology*
  • Nails, Malformed / genetics
  • Protein Serine-Threonine Kinases / genetics

Substances

  • Protein Serine-Threonine Kinases
  • CHUK protein, human
  • I-kappa B Kinase
  • IKBKB protein, human
  • IKBKE protein, human