Indian Journal of Paediatric Dermatology

CASE REPORT
Year
: 2018  |  Volume : 19  |  Issue : 1  |  Page : 77--79

Dermatopathia pigmentosa reticularis


Gauri Vats, Rohit Kataria, Durgesh Sonare, Vinod Jain 
 Department of Skin and VD, Dr. S.N. Medical College, Jodhpur, Rajasthan, India

Correspondence Address:
Durgesh Sonare
Room No. 94, PG Hostel, MDM Hospital Campus, Jodhpur, Rajasthan
India

Dermatopathia pigmentosa reticularis (DPR) is a rare disorder with characteristic triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. A 12-year-old Indian boy presented with classical features of the triad along with adermatoglyphia, hyperhidrosis, punctate hyperkeratosis of palm, and sole along with keratosis pilaris. Histopathology suggested a diagnosis of DPR with a differential of Naegeli–Franceschetti–Jadassohn syndrome and dyskeratosis congenita.


How to cite this article:
Vats G, Kataria R, Sonare D, Jain V. Dermatopathia pigmentosa reticularis.Indian J Paediatr Dermatol 2018;19:77-79


How to cite this URL:
Vats G, Kataria R, Sonare D, Jain V. Dermatopathia pigmentosa reticularis. Indian J Paediatr Dermatol [serial online] 2018 [cited 2019 Sep 20 ];19:77-79
Available from: http://www.ijpd.in/article.asp?issn=2319-7250;year=2018;volume=19;issue=1;spage=77;epage=79;aulast=Vats;type=0