Zobrazeno 1 - 10
of 37
pro vyhledávání: '"A. Ennejjar"'
Autor:
Ennejjar, Amine1, Moutamani, Salma1, Boutaj, Taha boutajtaha@gmail.com, Touil, Wiame2, Amazouzi, Abdellah1, Cherkaoui, Ouafa1
Publikováno v:
Pan African Medical Journal. Jan-Apr2022, Vol. 41, p1-6. 6p.
Publikováno v:
Journal Français d'Ophtalmologie. 45:977-979
Autor:
Salma Moutamani, Taha Boutaj, Amine Ennejjar, Wiame Touil, Abdellah Amazouzi, Ouafa Cherkaoui
Publikováno v:
Pan African Medical Journal; Vol. 41 No. 1 (2022)
Central retinal artery occlusion (CRAO) is a rare condition. It is a diagnostic and therapeutic emergency. CRAO is analogous to an acute stroke of the eye. The disease usually affects patients after 60 years of age, and rarely young persons. The risk
Publikováno v:
Journal francais d'ophtalmologie. 45(8)
Ocular coloboma is a rare malformation which occurs as an isolated defect in healthy individuals or be part of a complex malformation syndrome of known or unknown etiology. Patients with coloboma of iris and choroid complicated with cataract should h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::716daf186454c04610de63026e6ba6a7
Autor:
Ennejjar Amine, Taha Boutaj
Valsava maculopathy is one of many causes of premacular hemorrhage. This case report highlights the interest of multimodal imaging in the diagnosis of retinal emergencies which can engage the visual prognosis, especially in a young patient as in our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e7621501bfcdd3e0500c1c003a2246d
Autor:
Amine Ennejjar, Taha Boutaj
Publikováno v:
Pan African Medical Journal; Vol. 41 No. 1 (2022)
Il s´agit d´un patient de 36 ans, issus d'un mariage consanguin, ayant comme antécédent la maladie de Wilson dans ses trois formes cliniques, hépatique, neurologique et psychiatrique. L´examen ophtalmologique retrouve une acuité visuelle (AV)
Autor:
Amine, Ennejjar, Taha, Boutaj
Publikováno v:
The Pan African medical journal. 41
Autor:
Amine Ennejjar, Taha Boutaj
Publikováno v:
PAMJ Clinical Medicine. 8
Autor:
Amine Ennejjar, Salma Moutamani, Taha Boutaj, Wiame Touil, Abdellah Amazouzi, Ouafa Cherkaoui
Publikováno v:
Pan African Medical Journal; Vol. 41 No. 1 (2022)
Kearns-Sayre syndrome is a rare mitochondrial disorder. It had a triad of features, including progressive external ophthalmoplegia, pigmentary retinopathy, and an alteration of cardiac conduction. The ocular manifestations include bilateral ptosis, p