Dermatopathia pigmentosa reticularis (DPR): A rare case of late onset disease
Dermatopathia pigmentosa reticularis (DPR) is a rare inherited disorder presenting with the clinical triad of reticulate pigmentation, nail dystrophy and diffuse alopecia. The usual presentation of DPR is at birth or very early childhood (<2 years). A few cases of late-onset disease have been reported.
Deepani Rathnayake +2 more
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Inherited Reticulate Pigmentary Disorders. [PDF]
Lin MH +5 more
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Haber's Syndrome: A Case Report. [PDF]
Aljoudi SB, Tallab M, Al Hawsawi K.
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Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment. [PDF]
Kaiser M +5 more
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Sporadic Dyschromatosis Universalis Hereditaria: A Second Case Report From Iran. [PDF]
Dogohar S +4 more
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Dermoscopic and Onychoscopic Features of Dyskeratosis Congenita. [PDF]
Vasani R, Baddireddy K.
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Reticulated Hyperpigmentation as a Sign of Lichen Planopilaris. [PDF]
Goldman C +4 more
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Idiopathic Hypereosinophilic Syndrome Presenting with Recalcitrant Oral and Genital Ulcers Responding Well to Thalidomide. [PDF]
Srinivas SM, Chebbi PG, Shivappa SK.
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Two Cases of Dyskeratosis Congenita with Clinically Distinct Presentations, Seen in National University Hospital, Singapore. [PDF]
Juay L, Chandran NS.
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