Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Caroline Atef Tawfik"'
Publikováno v:
BMC Ophthalmology, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Inherited retinal diseases form a rare, highly heterogeneous group of genetic disorders characterized by retinal degeneration. It is considered one of the leading causes of debilitating visual loss and blindness in children and yo
Externí odkaz:
https://doaj.org/article/78419ca248084861bc1b6079b1e93e31
Publikováno v:
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-11 (2022)
Abstract Background Oguchi disease is a rare type of congenital stationary night blindness associated with an abnormal fundus appearance. It is inherited in an autosomal recessive manner where two types exist according to the gene affected; type 1 as
Externí odkaz:
https://doaj.org/article/bd4e86fecd8e402a9d4e6bfbaa2a37c3
Publikováno v:
Ophthalmic Genetics. 44:226-233
Publikováno v:
Journal of VitreoRetinal Diseases. 6:312-315
Purpose: To report a case of autosomal recessive bestrophinopathy (ARB) that presented with macular hole retinal detachment (MHRD). Methods: A case report. Results: A 31-year-old male patient presented with rapid deterioration of vision in the left e
Publikováno v:
Ophthalmology and Therapy
Introduction Exfoliation syndrome is an age-related disease leading to ocular and systemic complications. We aimed to evaluate the prevalence of exfoliation syndrome (XFS) in Egypt and its association with cataract as one of its comorbidities. Method