Results 1 to 10 of about 76 (46)

Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder

open access: yesIndian Dermatology Online Journal, 2013
Dermatopathia pigmentosa reticularis is a rare ectodermal dysplasia with a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
Vinay Shanker, Mudita Gupta
exaly   +5 more sources

Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review

open access: yesIndian Journal of Dermatology, 2016
Dermatopathia pigmentosa reticularis (DPR) is a very rare autosomal dominant ectodermal dysplasia caused by mutations in keratin 14 and characterized by the triad of generalized reticulate hyperpigmentation, nonscarring alopecia, and onychodystrophy.
Fahad Al Saif
exaly   +5 more sources

A Case of Dermatopathia Pigmentosa Reticularis [PDF]

open access: yesJournal of Dermatology, 1997
AbstractDermatopathia pigmentosa reticularis (DPR) is a very rare disorder with the diagnostic triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. Many other dermatologic findings have been associated with this triad, including adermatoglyphia, hypohidrosis or hyperhidrosis, palmoplantar hyperkeratosis, and ...
T S, Bu, Y K, Kim, K U, Whang
exaly   +23 more sources

Dermatopathia pigmentosa reticularis: a rare case

open access: yesPigment International, 2022
Dermatopathia pigmentosa reticularis (DPR) is a rare ectodermal dysplasia with a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
Nidhin Varghese, J. P Prathibha
doaj   +2 more sources

Dermatopathia pigmentosa reticularis: A rare case report and review of literature

open access: yesClinical Dermatology Review, 2022
Dermatopathia pigmentosa reticularis is a rare autosomal dominant disorder. It is an ectodermal dysplasia, characterized by a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
Aswath Rajan   +4 more
doaj   +2 more sources

Dermatopathia pigmentosa reticularis

open access: yesIndian Journal of Dermatology, 2019
Dermatopathia pigmentosa reticularis is a rare ectodermal dysplasia that presents with a triad of reticulate hyperpigmentation, nonscarring alopecia, and nail dystrophy.
Adrija Datta   +3 more
doaj   +3 more sources

Dermatopathia pigmentosa reticularis: through the eye of dermoscope

open access: yesPigment International, 2023
Dermatopathia pigmentosa reticularis is a rare ectodermal dysplasia characterized by a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. We report a case of a 22-year-old male with characteristic features of
Aditi Bansal   +3 more
doaj   +2 more sources

Dermatopathia Pigmentosa Reticularis with Addisonian Pigmentation

open access: yesIndian Dermatology Online Journal, 2022
Dermatopathia pigmentosa reticularis is a rare ectodermal dysplasia with mottled pigmentation. Here we report a case of 15-year-old boy with variable (reticulate as well as diffuse) pigmentary disorder and adermatoglyphia.
Taru Garg
exaly   +3 more sources

The Network of Mystery: Unraveling Atypical Dermatopathia Pigmentosa Reticularis

open access: yesClinical Dermatology Review
Dermatopathia pigmentosa reticularis (DPR) is a rare ectodermal dysplasia characterized by generalized reticulate hyperpigmentation, nonscarring alopecia, and onychodystrophy, caused by autosomal dominant mutations in KRT14. Fewer than 25 cases have been
Spandana Devarahalli Krishnamurthy   +3 more
doaj   +2 more sources

Dermatopathia pigmentosa reticularis: a rare case report

open access: yesPigment International
Dermatopathia pigmentosa reticularis (DPR) is a very rare ectodermal disorder with autosomal dominant mode of inheritance. It is associated with a mutation in the keratin 14 gene on chromosome 17. It is characterized by a diagnostic triad of generalized reticulate hyperpigmentation, non-cicatricial alopecia, and onychodystrophy. We hereby report a case
Suhail Khan   +2 more
exaly   +2 more sources

Home - About - Disclaimer - Privacy