Zobrazeno 1 - 10
of 77
pro vyhledávání: '"dermatopathia pigmentosa reticularis"'
Autor:
Nidhin Varghese, J. P Prathibha
Publikováno v:
Pigment International, Vol 9, Iss 3, Pp 220-224 (2022)
Dermatopathia pigmentosa reticularis (DPR) is a rare ectodermal dysplasia with a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. We report a case of a 21-year-old man who had generalized reticulate pig
Externí odkaz:
https://doaj.org/article/e1da464209db4c47bfe456c5e5840877
Publikováno v:
Clinical Dermatology Review, Vol 6, Iss 1, Pp 54-54 (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. The mode of inheritance is
Externí odkaz:
https://doaj.org/article/0a6c2664cea845b4ae0af6343d914eff
Publikováno v:
Indian Journal of Dermatology, Vol 64, Iss 2, Pp 149-151 (2019)
Dermatopathia pigmentosa reticularis is a rare ectodermal dysplasia that presents with a triad of reticulate hyperpigmentation, nonscarring alopecia, and nail dystrophy. We report herein a case of a 23-year-old male presenting with the characteristic
Externí odkaz:
https://doaj.org/article/56923a99cb6442259afd09640d593d1b
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 19, Iss 1, Pp 77-79 (2018)
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
Externí odkaz:
https://doaj.org/article/89471dd4acd34d848a029b704616e9d4
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 6, Pp 403-406 (2015)
Naegeli-Franceschetti-Jadassohn Syndrome (NFJS) is a rare, autosomal dominant inherited form of ectodermal dysplasia, caused by mutation in the KRT14 gene. We report here a case of NFJS in a 27-year-old male who presented with reticulate hyperpigment
Externí odkaz:
https://doaj.org/article/77d0e51a291a4561aa3e10ca3eefad5d
Publikováno v:
JAAD Case Reports
Dermatopathia pigmentosa reticularis (DPR) is an extremely rare autosomal dominant ectodermal dysplasia that occurs because of mutations in KRT14. It mainly affects the skin, nails, and hair, with a characteristic diagnostic triad of widespread retic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a012c4c66370d6eb2566ee347583747
https://doi.org/10.1016/j.jdcr.2019.02.014
https://doi.org/10.1016/j.jdcr.2019.02.014
Autor:
Vikarn Vishwajeet, Uma Nahar Saikia, Rahul Mahajan, Dipankar De, Reena Das, Manu Jamwal, Vinod Scaria, Anuradha Bishnoi
Publikováno v:
American Journal of Medical Genetics Part A. 185:278-281
A 9-year-old boy presented for evaluation of variegated skin pigmentation. Palms and soles revealed honeycombed hyperpigmented hyperkeratosis. Irregular, firm, skin coloured nodules suggestive of cutaneous calcification were present on both elbows. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dd641bc53f44aadad0de91125495acd
https://doi.org/10.1002/ajmg.a.61943
https://doi.org/10.1002/ajmg.a.61943
Autor:
Vinay Shanker, Mudita Gupta
Publikováno v:
Indian Dermatology Online Journal, Vol 4, Iss 1, Pp 40-42 (2013)
Dermatopathia pigmentosa reticularis is a rare ectodermal dysplasia with a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. We report a case of a 21 year old woman who had generalized reticulate pigment
Externí odkaz:
https://doaj.org/article/6a380d67be9847b39170104d3e5e1cd9
Akademický článek
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Autor:
Fahad Al Saif
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 4, Pp 468-468 (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.
Externí odkaz:
https://doaj.org/article/840737f02fa94959a5a74d14777cb8f6