Abstract |
Pachyonychia congenita is a distinct hereditary disorder of keratinization, in which dystrophy of all nails is associated with palmoplantar keratoderma and other hyperkeratoses. Recently a late-onset type has been reported. We report a second family with late-onset pachyonychia congenita, showing a remarkable clinical heterogeneity. Furthermore, one patient demonstrated a number of associated hyperkeratoses not previously recognized. Acitretin proved useful in the treatment of this late-onset form of pachyonychia congenita.
|
Authors | G P Lucker, P M Steijlen |
Journal | Clinical and experimental dermatology
(Clin Exp Dermatol)
Vol. 20
Issue 3
Pg. 226-9
(May 1995)
ISSN: 0307-6938 [Print] England |
PMID | 7671418
(Publication Type: Case Reports, Journal Article)
|
Topics |
- Family
- Humans
- Keratoderma, Palmoplantar
(pathology)
- Male
- Middle Aged
- Nail Diseases
(pathology)
- Syndrome
|