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

Dermatopathia pigmentosa reticularis


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
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijpd.IJPD_79_16

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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.


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