Dermatopathia Pigmentosa Reticularis
Authors:
- 1 September 2007
- journal article
- case report
- Published by Wiley in Pediatric Dermatology
- Vol. 24 (5) , 566-570
Abstract
Abstract: Dermatopathia pigmentosa reticularis is a rare inherited pigmentary disorder of the skin characterized by generalized reticulate hyperpigmentation, nonscarring alopecia and onychodystrophy. The reticulate pigmentation occurs at birth or during early childhood. We hereby report a 12‐year‐old Indian patient with this disorder.Keywords
This publication has 7 references indexed in Scilit:
- A Case of Dermatopathia Pigmentosa ReticularisThe Journal of Dermatology, 1997
- Dermatopathia pigmentosa reticularis: A report of a family demonstrating autosomal dominant inheritanceJournal of the American Academy of Dermatology, 1992
- Dermatopathia pigmentosa reticularisArchives of Dermatology, 1990
- Reticulate pigmentary disorders-a reviewClinical and Experimental Dermatology, 1984
- Dermatopathia pigmentosa reticularisClinical and Experimental Dermatology, 1977
- Hyperpigmentation and hypohidrosis. (THE NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME): REPORT OF A FAMILY AND REVIEW OF THE LITERATUREClinical and Experimental Dermatology, 1976
- Dermatopathia pigmentosa reticularis hyperkeratotica et mutilansDermatology, 1970