Results 61 to 70 of about 2,635 (188)

Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation family.

, 2003
AIMS: To report the detailed clinical findings in a three generation pedigree with autosomal dominant cataract, microcornea, and coloboma resulting from mutation of the lens development gene, MAF. METHODS: Five members of a three generation pedigree with
Jamieson, R.V., Farrar, N., Perveen, R., Balmer, A., Munier, F., Black, G.C.   +5 more
core   +1 more source

Unilateral acute hydrops in a child with bilateral microcornea and iridofundal coloboma

Indian Journal of Ophthalmology, 2019
A 15-year-old female child with history of bilateral poor vision since childhood presented with sudden onset pain, photophobia, and diminution of vision OD for 10 days. Visual acuity was hand motion OD and 1/60 OS.
Rinky Agarwal, Grisilda Nongrem, Prafulla K Maharana, Namrata Sharma   +3 more
doaj   +1 more source

Incidence and risk factors of rhegmatogenous retinal detachment following paediatric cataract surgery: A systematic review and meta‐analysis

Acta Ophthalmologica, Volume 103, Issue 7, Page 764-775, November 2025.
Abstract To determine the incidence and identify risk factors of rhegmatogenous retinal detachment (RRD) following paediatric cataract surgery. This systematic review and meta‐analysis adhered to PRISMA guidelines and was registered in PROSPERO (CRD42024538383). A comprehensive search was conducted across multiple databases, including Cochrane CENTRAL,
Hashem Abu Serhan, Saad Ashraf, Ayesha Shaukat, Ajeet Singh, Hasnaa Abdelrhem, Hamza Irfan, Fariha Arif, Abdullah Ahmed   +7 more
wiley   +1 more source

COL4A1‐Related Leukoencephalopathy and Microangiopathy: A Case Series of Two Palestinian Siblings

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT We report two Palestinian siblings with a pathogenic COL4A1 mutation, presenting with congenital cataracts, seizures, developmental delay, and antenatal intracerebral hemorrhages. Despite sharing the same genetic variant, they exhibited striking phenotypic variability.
Thkra Meshal, Amal M. Shawabka, Kareem lbraheem, Rosol Iwaiwi, Nissreen E. Thafer, Jinan H. Afana, Ahmad G. Hammouri, Osama Atawneh   +7 more
wiley   +1 more source

Coexistence of MRCS syndrome, extremely long axis and exfoliation syndrome: a case report and literature review

BMC Ophthalmology, 2023
Background The coexistence of MRCS (microcornea, retinal dystrophy, cataract, and posterior staphyloma) syndrome and extremely long axis is rare since microcornea frequently accompanies with diminution of entire anterior segment and occasionally the ...
Xinglin Wang, Xiaodan Jiang, Ziyuan Liu, Changguan Wang, Xuemin Li   +4 more
doaj   +1 more source

Pediatric Anesthetic Management of a Patient With Warburg Micro Syndrome, a Rare Autosomal Recessive Genetic Disorder

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Warburg micro syndrome is an extremely rare autosomal recessive genetic disorder with only 100 families documented worldwide. We present a safe and successful anesthetic management of a pediatric patient with Warburg micro syndrome utilizing total intravenous anesthesia (TIVA) and incisional Exparel.
Esha Thakkar, Michael McNally, Adrienne Hutton, Michael Holdeman, David G. Jackson   +4 more
wiley   +1 more source

Biometric characteristics of eyes with microcornea and congenital cataract

Delta Journal of Ophthalmology
Purpose The aim of this study was to report on the biometric characteristics of the eyes with congenital cataract (CC) and microcornea (suggesting a novel index to characterize the anterior segment of children eyes with CC) and to compare it to the ...
Nihal El Shakankiry, Nader Bayoumi, Nshokano S. Gloria   +2 more
doaj   +1 more source

Scleral Fixated Intraocular Lens in Aphakic Patient with Bilateral Microcornea and Microphthalmia

International Medical Case Reports Journal, 2021
Nada N Alwohaibi, Mohanna Y Aljindan, Fatimah N AlRashidi Ophthalmology Department, King Fahad Hospital of the University, Khobar, Eastern Province, Kingdom of Saudi ArabiaCorrespondence: Nada N AlwohaibiOphthalmology Department, King Fahad Hospital of ...
Alwohaibi NN, Aljindan MY, AlRashidi FN
doaj  

Anterior transposition of inferior oblique for inferior rectus muscle aplasia

Taiwan Journal of Ophthalmology, 2019
Congenital absence of extraocular muscle is rare. The most common extraocular muscle found to be congenitally absent is superior oblique followed by inferior rectus.
Anupam Singh, Ajai Agrawal, Sanjeev Kumar Mittal, Barun Kumar, Kartik Maheshbhai Rana, Rupal Verma   +5 more
doaj   +1 more source

Incidence of postoperative retinal detachment and bacterial endophthalmitis in the Swedish national paediatric cataract register and associated risk factors

Acta Ophthalmologica, Volume 103, Issue 5, Page 561-570, August 2025.
Abstract Purpose To investigate the incidence and risk factors of retinal detachment (RD) and bacterial endophthalmitis in a cohort of children who underwent cataract surgery before the age of eight. Methods Data was retrieved from the Swedish national paediatric cataract register.
Arzu Seyhan Karatepe Hashas, Anna Linnarsson Wiklund, Jenny Gyllén, Birgitte Haargaard, Gunilla Magnusson, Alf Nyström, Kristina Tornqvist, Eric Trocmé, Ulrika Kjellström   +8 more
wiley   +1 more source