Zobrazeno 1 - 10
of 79
pro vyhledávání: '"adermatoglyphia"'
Publikováno v:
罕见病研究, Vol 2, Iss 2, Pp 178-185 (2023)
Objective To summarize the clinical features of a family with Basan syndrome and to analyze mutation of the SMARCAD1 gene. Methods The Basan family was diagnosed at Dermatology Hospital, Southern Medical University in 2022. Backgroud data was collect
Externí odkaz:
https://doaj.org/article/eb1fed77501a444b934d90bddf7c9c06
Autor:
Masnicová, Soňa, Krajníková, Magdaléna
Publikováno v:
Forenzní vědy, právo, kriminalistika / Forensic sciences, law, criminology. 8(2):300-314
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=1134035
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
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:
Liaquat National Journal of Primary Care, Vol 3, Iss 1, Pp 39-40 (2021)
This is a case of Adermatoglyphia or simply a loss of fingerprints in a young female patient in her 20s having a condition of hyperhidrosis and atopic dermatitis. At a young age, this condition can be very frustrating and give the patient a red flag
Externí odkaz:
https://doaj.org/article/3430b0b8cb914ae19c44e82b1570367b
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
Autor:
Tanuj Kanchan, Kewal Krishan
Publikováno v:
Egyptian Journal of Forensic Sciences, Vol 8, Iss 1, Pp 1-2 (2018)
Abstract Fingerprints have been successfully used for identification purposes for more than a century and remained one of the most commonly recovered evidence at the scene of crime. Due to their uniqueness and individualistic characteristics, the fin
Externí odkaz:
https://doaj.org/article/d45d13882c0f48e693712c7ad92d18ea
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 3, Pp 210-212 (2015)
Reticulate acropigmentation of Kitamura (RAK) is a rare, autosomal dominant disorder first described in Japan characterised by a reticulate pattern of slightly atrophic, angulated, hyperpigmented macules affecting the acral areas of the body. We here
Externí odkaz:
https://doaj.org/article/0ca19904f62d49439f595ca0491b9d9b
Akademický článek
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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