Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Zoubida Mehsas"'
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:
Zoubida Mehsas, Soukaina Sektaoui, Meriem Meziane, Nadia Ismaili, Leila Benzekri, Karima Senouci
Publikováno v:
Our Dermatology Online. 13:148-151
Background: Patients with pemphigus receiving immunosuppressive therapy are considered at risk of developing severe forms of COVID-19. We aimed to analyze the clinical and evolutionary characteristics of COVID-19 infection in patients with pemphigus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5b4a20bf08798a95a0c9a7435b2805d
https://doi.org/10.7241/ourd.20222.6
https://doi.org/10.7241/ourd.20222.6
Publikováno v:
Scholars Journal of Medical Case Reports. 11:144-145
Carcinoma en cuirasse is a rare form metastatic cutaneous that characterized by a diffuse sclerodermoid induration of the mammary area, the chest and the abdomen. It is preferentially associated with a local recurrence of breast cancer after mastecto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a44617a951ad1727b62abc41546e7e8d
https://doi.org/10.36347/sjmcr.2023.v11i02.012
https://doi.org/10.36347/sjmcr.2023.v11i02.012