Zobrazeno 1 - 10
of 44
pro vyhledávání: '"I. Damoune"'
Publikováno v:
The Egyptian Journal of Otolaryngology, Vol 38, Iss 1, Pp 1-4 (2022)
Abstract Background Thyroid abscess is a rare entity and occurs in patients in a particular situation either in an immunocompromised patient or on tuberculosis infection since the African countries are still tuberculosis endemic countries Case presen
Externí odkaz:
https://doaj.org/article/348c0dc740884c1e80b1a052c6387f51
Non-classical congenital adrenal hyperplasia by 21 hydroxylase deficiency is an autosomal recessive disease whose usual presentation is a late virilization. In some African countries like Morocco, there are cultural barriers to gynecological examinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a22a51d9aca0dcf97b102f43e63ef0c
Publikováno v:
Annales d'Endocrinologie. 84:159
Publikováno v:
Annales d'Endocrinologie. 84:165
Obesity is considered a sign of beauty in some regions, especially in southern Morocco and some sub-Saharan countries,the use of glucocorticoids to gain weight is a common practice among women in these regions. We report the case of a female patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81307cec23f512b235d520f525a6346e
Publikováno v:
Annales d'Endocrinologie. 82:423
Publikováno v:
Annales d'Endocrinologie. 82:398
Publikováno v:
Annales d'Endocrinologie. 82:399
Publikováno v:
Annales d'Endocrinologie. 82:445
Introduction La polyendocrinopathie auto-immune de type 1 (APECED) est une dysregulation auto-immune des lymphocytes T auto-reactifs. Elle associe classiquement candidose cutaneomuqueuse, hypoparathyroidie et insuffisance surrenalienne. L’objectif
Publikováno v:
Annales d'Endocrinologie. 82:454
Introduction Le Syndrome de Turner est une affection genetique rare liee a l’absence totale ou partielle d’un chromosome X. Le tableau clinique est tres heterogene et la dysmorphie est souvent moderee, voire absente. L’objectif de ce travail es