| Autor: |
Gauri Vats, Rohit Kataria, Durgesh Sonare, Vinod Jain |
| Jazyk: |
angličtina |
| Rok vydání: |
2018 |
| Předmět: |
|
| Zdroj: |
Indian Journal of Paediatric Dermatology, Vol 19, Iss 1, Pp 77-79 (2018) |
| Druh dokumentu: |
article |
| ISSN: |
2319-7250 |
| DOI: |
10.4103/ijpd.IJPD_79_16 |
| Popis: |
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. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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