Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Moulay Abderrahmane Afifi"'
Autor:
Kaoutar Moutaouakkil, Hicham Abdellaoui, Btissam Arhoune, Karima Atarraf, Samira El Fakir, Ghita Yahyaoui, Mustapha Mahmoud, Moulay Abderrahmane Afifi, Bouchra Oumokhtar
Publikováno v:
African Journal of Paediatric Surgery, Vol 19, Iss 2, Pp 78-82 (2022)
Objective: We aimed to estimate the prevalence of Staphylococcus aureus producing Panton–Valentine leucocidin (PVL) isolated from children diagnosed with osteoarticular infections (OAIs), and to examine risk factors and clinical features. Methods:
Externí odkaz:
https://doaj.org/article/fae45fe74f4541789b879082998d5b9a
Autor:
Mohammed Tazi Charki, Zineb Oudrhiri, Hicham Abdellaoui, karima Atarraf, Moulay Abderrahmane Afifi
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 88, Iss , Pp 102528- (2023)
We report in the case a rare localisation of aneurysmal bone cyst in the internal side of the clavicle in 10 years old girl treated by block-resection and two stage reconstruction of the bone defect by the technique of induced membrane of Masquelet.
Externí odkaz:
https://doaj.org/article/785a2b299e9b466f98ed50b972f059a8
Autor:
Mohamed Amine Oukhouya, Mohammed Tazi Charki, Hicham Abdellaoui, Karima Atarraf, Moulay Abderrahmane Afifi
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 88, Iss , Pp 102531- (2023)
Popliteal pterygium syndrome is very rare genetic disorder, it can occur in multiple parts of the body, especially the kness with. This current case report describes a 14-day-old newborn admitted to the department of pediatric orthopaedic surgery for
Externí odkaz:
https://doaj.org/article/a8feb61ac8b24bb0bfbca011f1926a2e
Autor:
Kaoutar Moutaouakkil, Bouchra Oumokhtar, Hicham Abdellaoui, Samira El Fakir, Btissam Arhoune, Mustapha Mahmoud, Karima Atarraf, Moulay Abderrahmane Afifi
Publikováno v:
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background The progress of diagnostic strategies and molecular methods improved the detection of Kingella kingae in bone and joint infections, and now, Kingella kingae is being increasingly recognized as the most frequent cause of bone and j
Externí odkaz:
https://doaj.org/article/9469cc3cc96a433cbeac40010f242d0f
Autor:
Hicham Ajdar, Tayeb Bentayeb, Mohamed Tazi Charki, Hicham Abdellaoui, Karima Atarraf, Moulay Abderrahmane Afifi
Publikováno v:
Foot & Ankle Surgery: Techniques, Reports & Cases, Vol 2, Iss 3, Pp 100207- (2022)
Osteochondroma of the navicular bone is a rare entity in the literature; it is often asymptomatic. A standard X-ray can make the diagnosis. The CT or rather MRI gives more details of this tumor and its relationship with the other elements of the ento
Externí odkaz:
https://doaj.org/article/27e017f2544f4db8b11018873093fee6
Publikováno v:
International Journal of Mycobacteriology, Vol 3, Iss 1, Pp 57-59 (2014)
Osteoarticular tuberculosis represents 1.7–2% of all tuberculosis (TB). The localization in the foot is rare and accounts for less than 10% of osteoarticular TB. The following report describes the case of a 7-year-old boy who presented with a gradu
Externí odkaz:
https://doaj.org/article/51e9a3b14caa4109af07b4471b980760
Publikováno v:
The Pan African Medical Journal, Vol 19, Iss 293 (2014)
Jeune fille âgée de 14 ans, présentant une déformation de la cuisse droite évoluant depuis l'âge de 2 ans et d'aggravation progressive. L'examen clinique a trouvé des sclérotiques bleus et une déformation de la cuisse droite avec une inégal
Externí odkaz:
https://doaj.org/article/8bbf3b6ea4c5414f8c4e52a31aaea921
Publikováno v:
The Pan African Medical Journal, Vol 18, Iss 319 (2014)
Le décollement épiphysaire post infectieux est une pathologie très rare, jamais décrite dans la littérature. Nous rapportons deux cas colligés au service : le 1er concerne un garçon âgé de 3 ans, admis pour impotence fonctionnelle du membre
Externí odkaz:
https://doaj.org/article/5c156288cbb340dbacb2a231c3c122be
Publikováno v:
The Pan African Medical Journal, Vol 12, Iss 22 (2012)
La dysplasie fibreuse est une maladie osseuse rare, elle représente environ 2,5% des maladies osseuses et 7% des tumeurs osseuses. Nous rapportons le cas d'un enfant âgé de 10 ans, admis pour prise en charge d'une tuméfaction sus claviculaire dro
Externí odkaz:
https://doaj.org/article/d79307c20f5b42ad937b60f8abe8ea70
Autor:
Mohamed Amine Oukhouya , Hicham Abdellaoui, Mohammed Tazi , Karima Atarraf and Moulay Abderrahmane Afifi
Background:Congenital short femur is characterized by a global femoral hypoplasia, classified in 5 types, type1 is a simple hypoplasia, revealed in our patient in the context of a fracture. Clinical case:The article presents a clinical observation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93a224855b83fbc37f46b1fbfcc2159e