Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Loubna, El Maaloum"'
Publikováno v:
The Pan African Medical Journal, Vol 32, Iss 177 (2019)
Les Molluscums contagiosum (MC) sont des lésions cutanées bénignes causées par Molluscipoxvirus, ils affectent principalement les enfants et les adultes jeunes et intéressent surtout la peau et rarement les muqueuses. Le diagnostic clinique est
Externí odkaz:
https://doaj.org/article/01ee01820ae942b7bd1116a27b046b9d
Publikováno v:
European Journal of Ophthalmology. 31:2796-2807
Primary congenital glaucoma (PCG) is a rare and severe form of glaucoma and is usually transmitted as an autosomal-recessive disease. However, PCG is more common in certain ethnic and geographic groups where consanguineous relationships are common. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::218200f322d45532b9bfcb7cb98826f2
https://doi.org/10.1177/11206721211016308
https://doi.org/10.1177/11206721211016308
Autor:
Fidélia Nihad, Da Silva, Lafia Xavier, Kora, Tania, Elongo, Asmaa, El Kebir, Loubna, El Maaloum, Nisrine, Bennani-Guebessi, Bouchra, Allali, Asmaa, El Kettani, Mehdi, Karkouri
Publikováno v:
Cureus.
Retinoblastoma (RB) is the most common intraocular primary malignancy for infants and young children. The tumor is bilateral in 40% of cases and unilateral in 60% of cases. The hereditary form is due to a germinal mutation in the RB1 tumor suppressor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0c90b48d8644d96450df87899617aff
https://doi.org/10.7759/cureus.25422
https://doi.org/10.7759/cureus.25422
Publikováno v:
International Journal of Surgery Case Reports
Introduction Ocular rosacea is a multifactorial disease. Its pathophysiology remains unclear. The ocular manifestations of rosacea are not specific and can range from simple blepharoconjunctivitis to sight-threatening such as corneal perforation. Cas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ecb37efeec2056cd5d81a9803439bec
https://pubmed.ncbi.nlm.nih.gov/34920319
https://pubmed.ncbi.nlm.nih.gov/34920319
Publikováno v:
European journal of ophthalmology. 31(6)
Primary congenital glaucoma (PCG) is a rare and severe form of glaucoma and is usually transmitted as an autosomal-recessive disease. However, PCG is more common in certain ethnic and geographic groups where consanguineous relationships are common. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd41f70d37f0fc7238f3270f4170c025
https://pubmed.ncbi.nlm.nih.gov/34020567
https://pubmed.ncbi.nlm.nih.gov/34020567
Autor:
Loubna El Maaloum, Soukaina Amrani, Bouchra Allali, Asmae El Kettani, Hind Hamdani, Ayoub Redouan
Publikováno v:
European Journal of Medical and Health Sciences. 2
Donnai-Barrow syndrome is an autosomal recessive disease due to mutations in the LRP2 gene described by Donnai and Barrow in 1993. We report through this clinical case the various ophthalmologic and extraocular manifestations of Donnai Barrow syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9119604565242e37d0ff5bec205ac1ad
https://doi.org/10.24018/ejmed.2020.2.6.605
https://doi.org/10.24018/ejmed.2020.2.6.605
Publikováno v:
International Journal of Surgery Case Reports. 92:106845
Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) is a rare autosomal dominant genetic disorder characterized by complex orbito-palpebral anomalies. We report a rare case of BPES associated with bilateral congenital cataract.This study repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dab902000babfc2a5e915daa3c3955cf
https://doi.org/10.1016/j.ijscr.2022.106845
https://doi.org/10.1016/j.ijscr.2022.106845
Publikováno v:
European Journal of Medical and Health Sciences. 2
X-linked retinoschisis (XLRS) is a rare, hereditary, and bilateral vitreoretinal degeneration, associating maculopathy and vitreoretinopathy. We report the case of X-linked retinoschisis diagnosed after congenital cataract surgery in a child.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e2f4a69b83e42ed4f381a7d4f82e87d
https://doi.org/10.24018/ejmed.2020.2.6.584
https://doi.org/10.24018/ejmed.2020.2.6.584
Autor:
Loubna El Maaloum, Bouchra Allali, Hind Hamdani, Ayoub Redouan, Mehdi El Kerkouri, Asmae El Kettani
Publikováno v:
European Journal of Medical and Health Sciences. 3:44-45
Tuberculosis is a frequent disease in Morocco, palpebral localization remains very rare, often poorly managed because of its polymorphism. We report the case of a 6-year-old patient, without any notable antecedents, who presented repeated chalazions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e28286becc4312934cd67d876a57d9d9
https://doi.org/10.24018/ejmed.2021.3.1.707
https://doi.org/10.24018/ejmed.2021.3.1.707
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