Zobrazeno 1 - 10
of 46
pro vyhledávání: '"A. Asermouh"'
Autor:
Chaimae Ait Khabba, MD, Marwa Asermouh, MD, Mariame Meziane, MD, Laila. Benzekri, MD, Karima Senouci, MD
Publikováno v:
JAAD Case Reports, Vol 39, Iss , Pp 37-39 (2023)
Externí odkaz:
https://doaj.org/article/293bf9b1b75d4c7e98fb6021d0957554
Publikováno v:
Nasza Dermatologia Online, Vol 14, Iss e, Pp e45-e45 (2023)
Externí odkaz:
https://doaj.org/article/04eb57aa842c403c86f43cc412233bd1
Publikováno v:
Asian Journal of Pediatric Research. 12:32-35
Aims: Pachyonychia congenita is a rare genodermatosis related to mutations in the genes encoding keratins. Illustrations of such a typical case of this uncommon condition have rarely been seen in the literature, hence the interest of our case report.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a78f3f7ece702a29b867c1b29981572a
https://doi.org/10.9734/ajpr/2023/v12i1232
https://doi.org/10.9734/ajpr/2023/v12i1232
Autor:
Marwa Asermouh, Safae Maouni, Chaimae Ait Khabba, Kaoutar Znati, Karima Senouci, Mariame Meziane
Publikováno v:
Asian Journal of Pediatric Research. 12:28-31
Aims: Solitary nodular calcinosis of Winer is a rare and benign form of localized idiopathic cutaneous calcinosis. Its dermoscopic features may be useful for early diagnosis, but have never been described in the literature to our knowledge. Case Repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8187923d770575999bbfdb513152ceec
https://doi.org/10.9734/ajpr/2023/v12i1231
https://doi.org/10.9734/ajpr/2023/v12i1231
Publikováno v:
Asian Journal of Pediatric Research. 11:11-15
Aims: Pityriasis lichenoides chronic is a rare inflammatory dermatosis, unusually hypochromic in dark phototypes. The evolution of the disease is usually benign, but a malignant transformation in mycosis fungoides is reported. You have to know how to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ebe883ce25b9a5bb7f4067e30467936
https://doi.org/10.9734/ajpr/2023/v11i4226
https://doi.org/10.9734/ajpr/2023/v11i4226
Publikováno v:
Asian Journal of Pediatric Research. 11:1-5
Aim: Onychomycosis is a rare pathology in infants which constitutes 15.5% of onychodystrophies in children, especially those with Down syndrome and the immunocompromised. Dermosocpy is an innocuous examination allowing to guide the clinical diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b44cb64cb554dcdafbe424fdf7cf31ac
https://doi.org/10.9734/ajpr/2023/v11i4224
https://doi.org/10.9734/ajpr/2023/v11i4224
Autor:
Ait Khabba Chaimae, Mehsas Zoubida, Asermouh Marwa, Meziane Meriem, Ismaili Nadia, Benzekri Laila, Senouci Karima
Publikováno v:
International Journal of Research in Dermatology. 9:142-144
Vesiculo-bullous lesions as well as the late onset are extremely rare features of Darier disease (DD) making positive diagnosis more difficult. Its association with polycythemia vera prompts to look for signs suggestive of malignant hematological tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eae6cd3e80d50c1a897d1d71e1e54e11
https://doi.org/10.18203/issn.2455-4529.intjresdermatol20231171
https://doi.org/10.18203/issn.2455-4529.intjresdermatol20231171
Publikováno v:
In JAAD Case Reports September 2023 39:37-39
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 2:A249-A250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98d90a52d86b5b9ca10ce0bd8f440244
https://doi.org/10.1016/j.fander.2022.10.074
https://doi.org/10.1016/j.fander.2022.10.074
Publikováno v:
Asian Journal of Pediatric Research. :33-36
Rat-bite fever (RBF) is a systemic infectious disease. It is due to Streptobacillus moniliformis, a commensal bacterium of the nasopharyngeal mucosa of small rodents, in particular rats. This anthropozoonosis is rare in urban areas. The first clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a54d68d5d3813b86d62e1728b69f728d
https://doi.org/10.9734/ajpr/2020/v3i230126
https://doi.org/10.9734/ajpr/2020/v3i230126