Zobrazeno 1 - 10
of 81
pro vyhledávání: '"reticulate pigmentation"'
Publikováno v:
Dermatology Reports (2024)
Reticulate pigmentary disorders can be classified into inherited or acquired and cutaneous drug- induced reticulate hyperpigmentation belongs to this last group. The list of the drugs involved is constantly increasing and chemotherapy agents are freq
Externí odkaz:
https://doaj.org/article/71fcd068c15e43efb70c99fad421053a
Publikováno v:
Pigment International, Vol 10, Iss 3, Pp 172-178 (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 feature
Externí odkaz:
https://doaj.org/article/5a65304efa31461faf6e352ffea9d8e3
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:
JAAD Case Reports, Vol 6, Iss 5, Pp 457-461 (2020)
Externí odkaz:
https://doaj.org/article/7d5cd55177194991a133b4d6e65a4601
Publikováno v:
Indian Journal of Dermatology, Vol 64, Iss 3, Pp 235-238 (2019)
Naegeli–Franceschetti–Jadassohn syndrome is a rare autosomal dominant form of ectodermal dysplasia affecting sweat glands, nails, teeth, and skin. We report a case of 16-year-old female who had generalized reticulate pigmentation, dental changes,
Externí odkaz:
https://doaj.org/article/08e99aa94e8e4972b7b97fd05e6e11e8
Akademický článek
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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:
Clinical Dermatology Review, Vol 6, Iss 2, Pp 153-153 (2022)
Reticulate acropigmentation of Dohi is a rare genodermatosis inherited as an autosomal dominant trait. It is a localized form of dyschromatosis universalis hereditarian, characterized by the presence of hyperpigmented and hypopigmented macules with s
Externí odkaz:
https://doaj.org/article/3c9ea03b77a04eb2b607c90220a46151
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 Dermatology Online Journal, Vol 6, Iss 2, Pp 105-109 (2015)
Dyschromatosis universalis hereditaria (DUH) is a rare, autosomal dominant genodermatosis with a peculiar reticulate pigmentary change, consisting of hyperpigmented macules mingled with hypopigmented lesions to give an overall impression of mottling.
Externí odkaz:
https://doaj.org/article/066892bffcb9413bab0c24f021bf2c4c