Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Salma Bajjouk"'
Autor:
Salma Bajjouk, Mounia Bouchaar, Soukaina Haddougui, Fouad Elasri, Karim Reda, Abdelbarre Oubaaz
Publikováno v:
Journal de la Société Marocaine d’Ophtalmologie, Vol 0, Iss 29, Pp 19-21 (2020)
La rougeole est une pathologie virale du sujet jeune liée à une infection par un paramyxovirus. La rougeole systémique passe par quatre phases : incubation, invasion, éruption et desquamation. C’est une maladie essentiellement bénigne du point
Externí odkaz:
https://doaj.org/article/108f971311d34caa8c86d99c2a232ac9
Autor:
Soukaina Haddougui, Houda Brarou, Salma Bajjouk , Mounia Bouchaar, Yassine Mouzari and Abdelbarre Oubaaz
Bests disease is an autosomal dominant hereditary macular dystrophy characterized by the presence of auto-fluorescent vitelline deposits. We report a case of a vitelliform stage of bests disease in a 23-year-old female patient.The diagnosis was made
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa15bed5db17ea15ff5723697444fab
Autor:
Soukaina Haddougui, Mounia Bouchaar, Salma Bajjouk, Yassine Mouzari, Karim Reda, Abdelbarre Oubaaz
Publikováno v:
European Journal of Medical and Health Sciences. 5:1-2
We report an observation of an uncommon form of extra-papillary myelin fibers of fortuitous discovery in a patient, 55 years old, who consulted for a change of correction. The clinical aspect of the fundus led to the diagnosis of retinal myelin fiber
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c754ea2e1df55e4666c39ed7e5b8114d
https://doi.org/10.24018/ejmed.2023.5.1.1579
https://doi.org/10.24018/ejmed.2023.5.1.1579
Autor:
Mehdi Khamaily, Salma Bajjouk, Mounia Bouchaar, Mounir Belmalih, Karim Reda, Abdelbarre Oubaaz
Publikováno v:
European Journal of Medical and Health Sciences. 2
Pigmentary retinopathy refers to a group of inherited degenerative diseases of the retina, which primarily affects the photoreceptor cells in the retina. The association with congenital hearing loss defines Usher syndrome. Usher syndrome is a rare pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1adc4be2a84626bf66cf8c64ca0eaa94
https://doi.org/10.24018/ejmed.2020.2.4.380
https://doi.org/10.24018/ejmed.2020.2.4.380