Zobrazeno 1 - 10
of 883
pro vyhledávání: '"Angiofibromas"'
Publikováno v:
The Egyptian Journal of Otolaryngology, Vol 39, Iss 1, Pp 1-4 (2023)
Abstract Background Angiofibroma is a rare, histologically benign but locally aggressive vascular tumour that typically arises within the nasopharynx. Angiofibroma in sites other than the nasopharynx is extremely uncommon. Despite the histological si
Externí odkaz:
https://doaj.org/article/377cd0b5643a40baa995382cb392884b
Akademický článek
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Publikováno v:
Galicia Clínica, Vol 84, Iss 3, Pp 24-24 (2023)
ABSTRACT La esclerosis tuberosa es un síndrome genético infrecuente caracterizado por la mutación patogénica de los genes TSC1 o TSC2, que condiciona la activación descontrolada de la vía mTOR y la aparición subsecuente de hamartomas. Presenta
Externí odkaz:
https://doaj.org/article/1777ae70775042199a041b3249370035
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Tuberous Sclerosis Complex (TSC) is a genetic condition which leads to a loss of inhibition of cellular growth. Facial angiofibromas (FAs) are hamartomatous growths associated with TSC that appear as multiple small, erythematous papules on the skin o
Externí odkaz:
https://doaj.org/article/2f36978b782d400fa0cfc749864b06c7
Publikováno v:
Chinese Journal of Plastic and Reconstructive Surgery, Vol 3, Iss 1, Pp 41-45 (2021)
ABSTRACT: Tuberous sclerosis complex is a type of genetic multisystem disease that causes hamartomas in various organs. Facial angiofibromas commonly occur in 80% of patients and are prominently distributed over the cheek, chin, and nasolabial folds
Externí odkaz:
https://doaj.org/article/10068a0a8eaa4c278fbc7550429013fc
Publikováno v:
Galicia Clínica, Vol 82, Iss 1, Pp 26-29 (2021)
La Esclerosis Tuberosa (ET) ó Complejo Esclerosis Tuberosa es un trastor- no genético autosómico dominante que afecta a niños y adultos. Se debe a la ausencia parcial o total de la expresión de los genes TSC1 (hamartina) o TSC2 (tuberina), lo qu
Externí odkaz:
https://doaj.org/article/1de019c7404346828a73c5dbd6b5d10e
Autor:
Mari Wataya-Kaneda, Hiroshi Nagai, Yuuki Ohno, Hiroo Yokozeki, Yasuyuki Fujita, Hironori Niizeki, Kazue Yoshida, Masaaki Ogai, Yuichi Yoshida, Akihiko Asahina, Kazuyoshi Fukai, Chiharu Tateishi, Izumi Hamada, Tatsuro Takahata, Kenji Shimizu, Shigeki Shimasaki, Hiroyuki Murota
Publikováno v:
Dermatology and Therapy, Vol 10, Iss 4, Pp 635-650 (2020)
Abstract Introduction Our previous clinical studies have demonstrated the short-term efficacy and safety of the sirolimus gel for patients with tuberous sclerosis complex (TSC). However, long-term clinical evidence is lacking. Our objective was to as
Externí odkaz:
https://doaj.org/article/71187a866eb04dbdad37e301feef95c2
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 32, Iss 3, Pp 303-307 (2020)
Encephalotrigeminal Angiomatosis, also known as Sturge Weber Syndrome (SWS), Dimitri disease, Sturge Kalischer Weber Syndrome is specifically non familial, congenital rare disorder consisting of hamartomatous malformations that may affect eye, skin,
Externí odkaz:
https://doaj.org/article/e0ddcf7552144f479e3d075b5187ca19
Autor:
Livia-Cristiana Băicoianu-Nițescu, Ana-Maria Gheorghe, Mara Carsote, Mihai Cristian Dumitrascu, Florica Sandru
Publikováno v:
Diagnostics, Vol 12, Iss 11, p 2768 (2022)
Non-endocrine findings in patients with MEN1 (multiple endocrine neoplasia) syndrome also include skin lesions, especially tumor-type lesions. This is a narrative review of the English-language medical literature including original studies concerning
Externí odkaz:
https://doaj.org/article/59f5a4aa93ae4e49bdda354036ecf3ed
Autor:
Guillaume Le Guyader, Bernard Do, Ivo B. Rietveld, Pascale Coric, Serge Bouaziz, Jean-Michel Guigner, Philippe-Henri Secretan, Karine Andrieux, Muriel Paul
Publikováno v:
Pharmaceutics, Vol 14, Iss 3, p 569 (2022)
Facial angiofibromas (FA) are one of the most obvious cutaneous manifestations of tuberous sclerosis complex. Topical rapamycin for angiofibromas has been reported as a promising treatment. Several types of vehicles have been used hitherto, but polym
Externí odkaz:
https://doaj.org/article/51227dd701c843f8b047dc46ce9e5319