Zobrazeno 1 - 10
of 472
pro vyhledávání: '"atrophoderma"'
Publikováno v:
Journal of Nepal Medical Association, Vol 62, Iss 275 (2024)
Linear Atrophoderma of Moulin is a rare skin condition that is characterized by the development of one or more atrophic patches or depressions in the skin. These patches are usually located on the trunk, but they can also occur on the arms, legs, and
Externí odkaz:
https://doaj.org/article/c0e525b0d58647829103a5ccb6822a99
Publikováno v:
Clinical, Cosmetic and Investigational Dermatology, Vol Volume 16, Pp 193-196 (2023)
Chenyu Tang,1 Ping Wang2 1Department of Dermatology, Hangzhou Third People’s Hospital, Zhejiang Chinese Medical University, Hangzhou, People’s Republic of China; 2Department of Dermatology, Hangzhou Third People’s Hospital; Affiliated Hangzhou
Externí odkaz:
https://doaj.org/article/1275ef7551b741199e8b3b06eef0d934
Publikováno v:
Dermatology Practical & Conceptual, Vol 12, Iss 2 (2022)
Externí odkaz:
https://doaj.org/article/822ded5667cd41b1a2d7d6eaf9cca8a7
Akademický článek
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Autor:
Tasleem Arif
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 20, Iss 1, Pp 60-63 (2019)
Idiopathic atrophoderma of Pasini and Pierini (IAPP) is a rare disease of unknown etiology characterized by well-defined atrophic plaques with a “cliff-drop” border that show no signs of inflammation, sclerosis, and induration. The trunk is most
Externí odkaz:
https://doaj.org/article/d9ec9258cd0247c4b6e2f3181bddbde3
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 20, Iss 3, Pp 261-266 (2019)
Linear atrophoderma of Moulin (LAM) is a rare clinical entity characterized by hyperpigmented, depressed band-like skin lesions following blaschko lines (BL). Since its first description by Moulin et al., several authors have presented cases with var
Externí odkaz:
https://doaj.org/article/ad98516428e74325aae66dfcc72077c0
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 78, Iss 6 (2021)
Background: Linear atrophoderma of Moulin (LAM) is a dermatosis that affects children and adolescents characterized by hyperpigmented and atrophic linear lesions following Blaschko lines. So far, less than 50 cases have been published. Therefore, it
Externí odkaz:
https://doaj.org/article/dddcfa2371df442c979db1aed750cd76
Autor:
Yanshan Liu, Siddharth Banka, Yingzhi Huang, Jonathan Hardman-Smart, Derek Pye, Antonio Torrelo, Glenda M. Beaman, Marcelo G. Kazanietz, Martin J. Baker, Carlo Ferrazzano, Chenfu Shi, Gisela Orozco, Stephen Eyre, Michel van Geel, Anette Bygum, Judith Fischer, Zosia Miedzybrodzka, Faris Abuzahra, Albert Rübben, Sara Cuvertino, Jamie M. Ellingford, Miriam J. Smith, D. Gareth Evans, Lizelotte J.M.T. Weppner-Parren, Maurice A.M. van Steensel, Iskander H. Chaudhary, D. Chas Mangham, John T. Lear, Ralf Paus, Jorge Frank, William G. Newman, Xue Zhang
Publikováno v:
British Journal of Dermatology, 187(6), 948-961. Wiley
Background Bazex–Dupré–Christol syndrome (BDCS; MIM301845) is a rare X-linked dominant genodermatosis characterized by follicular atrophoderma, congenital hypotrichosis and multiple basal cell carcinomas (BCCs). Previous studies have linked BDCS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce266f5315a5c98055d5aabca2e9efeb
https://doi.org/10.1111/bjd.21842
https://doi.org/10.1111/bjd.21842
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 0, Iss 4, Pp 66-73 (2017)
The article analyzes the literature on polymorbidity of immune dermatoses. They confirm the possibility of combining with each other immune diseases, due to the presence of immune and metabolic abnormalities that are characteristic for the majority o
Externí odkaz:
https://doaj.org/article/7c64db5a2f3f4a3a93af379c50f51dc5