Zobrazeno 1 - 10
of 39
pro vyhledávání: '"H. Skiker"'
Autor:
Mina Laghmari, S. Ahid, R. Bezad, H. Skiker, K. Ouazzani Chahdi, B. Mansouri, Rajae Daoudi, B. Ouazzani Tnacheri, R. Lachkar, O. Cherkaoui, R. Abouqal, Y. Salhi, H. Alami, W. Ibrahimy, H. Handor
Publikováno v:
Journal Français d'Ophtalmologie. 37:313-319
Resume But de l’etude Evaluer la prevalence, la morphologie et la distribution des hemorragies retiniennes chez le nouveau-ne normal ainsi que leur relation avec les facteurs neonataux, maternels et obstetricaux, et determiner leur histoire naturel
Autor:
M, Laghmari, H, Skiker, H, Handor, B, Mansouri, K, Ouazzani Chahdi, R, Lachkar, Y, Salhi, O, Cherkaoui, B, Ouazzani Tnacheri, W, Ibrahimy, H, Alami, R, Bezad, S, Ahid, R, Abouqal, R, Daoudi
Publikováno v:
Journal francais d'ophtalmologie. 37(4)
To assess the prevalence, morphology and distribution of retinal hemorrhages in healthy newborns and their relationship to neonatal, maternal and obstetrical factors, and to determine their natural history.The present study prospectively included 2,0
Autor:
H, Skiker, W, Ibrahimy, N, Boutimzine, M, Laghmari, M, Benharbit, B, Tnacheri Ouazani, R, Daoudi
Publikováno v:
Bulletin de la Societe belge d'ophtalmologie. (308)
Connective tissues disorders are various and characterized by skin hyperelasticity, joint hypermobility and easy bruising. Ocular abnormalities predominate in type VI Ehlers-Danlos syndrome, Marfan disease, brittle cornea, Lobstein syndrome. We repor
Publikováno v:
Bulletin de la Societe belge d'ophtalmologie. (307)
Sarcoidosis is a multisystemic granulomatous disorder affecting young adults. It is very unfrequent in children. The authors report the case of an 11-year-old boy with a history of a pulmonary affection who was referred from the department of paediat
Publikováno v:
Journal francais d'ophtalmologie. 31(3)
Duane's syndrome is a congenital form of strabismus characterized by horizontal eye movement limitation and specifically by globe retraction with palpebral fissure narrowing in attempted adduction. It is usually associated with ocular and systemic pa
Publikováno v:
Bulletin de la Societe belge d'ophtalmologie. (306)
Wolfram syndrome, also known as DIDMOAD syndrome, is a rare disease characterized by the association of diabetes mellitus, diabetes insipidus, optic atrophy and deafness. The ophthalmologic findings are largely dominated by optic atrophy. Through fou
Publikováno v:
Bulletin de la Societe belge d'ophtalmologie. (306)
The open globe injuries in children are frequent and serious accidents. The purpose of this study is to investigate the epidemiologic and clinical characteristics and the visual outcomes of this accident. A retrospective study was conducted on 62 cas
Autor:
M, Lezrek, H, Skiker, S, Tachfouti, A, Karim, A, Karmane, Z, Bencherif, W, Cherkaoui, Z, Mohcine
Publikováno v:
Journal francais d'ophtalmologie. 28(9)
Primitive neuroectodermal tumor (PNET) of the orbit is rare. We present a case of a young patient with orbital PNET extending to the endo-crane and sinuses, which had been treated 10 years before with the diagnosis of rhabdomyosarcoma. The diagnosis
Publikováno v:
Annales d'Endocrinologie. 75:346
Introduction Les maladies osseuses constitutionnelles forment un groupe heterogene d’affections responsables d’insuffisances staturales associees ou non a des deformations, ou d’anomalies de la structure de l’os. Nous rapportons le cas d’un
Autor:
Mina Laghmari, H. Skiker, Rajae Daoudi, Y. Amrani, H. Mousaif, N. Handor, A. Karmane, F. El Maalam
Publikováno v:
Journal Français d'Ophtalmologie. 31:940-941