Zobrazeno 1 - 10
of 282
pro vyhledávání: '"Microspherophakia"'
Autor:
M Hemanandini, A Fathima Fahima
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 62, Iss 2, Pp 258-259 (2024)
Isolated sulphite oxidase deficiency is an autosomal recessive hereditary disorder. A 5-month-old male child with neonatal seizures and global developmental delay was referred by a paediatrician for ophthalmological evaluation. On examination, the ch
Externí odkaz:
https://doaj.org/article/2925ada880ac4b1585b3b34dff9bbb0b
Autor:
Rojananuangnit K, Rojnueangnit K
Publikováno v:
The Application of Clinical Genetics, Vol Volume 16, Pp 165-170 (2023)
Kulawan Rojananuangnit,1,* Kitiwan Rojnueangnit2,* 1Glaucoma Unit, Department of Ophthalmology, Mettapracharak (Wat Rai Khing) Hospital, Nakhon Pathom, Thailand; 2Division of Genetics, Department of Pediatrics, Faculty of Medicine, Thammasat
Externí odkaz:
https://doaj.org/article/ea04b68041814859943b5698b5a03383
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 13, Iss 4, Pp 479-488 (2023)
The crystalline lens is an important structure in the eye that starts to develop as early as the 22nd day of gestation, with further differentiation that continues after the induction. Congenital anomalies of the lens may involve the size, shape, and
Externí odkaz:
https://doaj.org/article/816d235759bc4eda82f6ba798e815d2b
Publikováno v:
International Journal of Ophthalmology, Vol 15, Iss 12, Pp 1944-1950 (2022)
AIM: To evaluate the safety and efficacy of scleral-fixated 3-looped haptics intraocular lens (IOL) implantation for surgical management of microspherophakia. METHODS: A retrospective case series include 10 microspherophakic patients (15 eyes) who un
Externí odkaz:
https://doaj.org/article/25f571c5470a482394bc68106d27e668
Abnormal lens thickening in a child with Weill–Marchesani syndrome 4: A 3-year follow-up case report
Autor:
Junting Huang, Kailai Nie, Xinpin Lv, Yuting Liu, Guiqi Yang, Junjiang Fu, Longqian Liu, Hongbin Lv
Publikováno v:
Frontiers in Medicine, Vol 9 (2023)
BackgroundWeill–Marchesani syndrome 4 (WMS4) is caused by ADAMTS17 gene variant and clinical abnormalities including lenticular myopia, ectopia lentis, glaucoma, microspherophakia, brachydactyly, and short stature. Due to free of heart defects and
Externí odkaz:
https://doaj.org/article/ebe150c6d8444be1a1839dae707669e6
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 11, Iss 12, Pp 7949-7952 (2022)
Microspherophakia refers to a spherophakic lens with a decreased equatorial diameter. Microspherophakia can be found in systemic or ocular conditions, such as Marfan's syndrome, Weill–Marchesani syndrome, iridocorneal endothelial syndrome, and Axen
Externí odkaz:
https://doaj.org/article/8b399fbb698b4d468946373316080976
Publikováno v:
Indian Journal of Ophthalmology, Vol 70, Iss 10, Pp 3677-3680 (2022)
We herein describe the kissing MVR technique in cases of microspherophakia for safe and effective endocapsular lens aspiration. Microspherophakia is associated with abnormally lax and broken zonules, which pose a great challenge to the operating surg
Externí odkaz:
https://doaj.org/article/79ac19baec094677ad24554f4b7a74ab
Publikováno v:
Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2262-2271 (2022)
Microspherophakia is a rare developmental abnormality of the crystalline lens with a myriad of ocular and systemic associations. Glaucoma is a serious complication associated with this disorder. Early identification of the disease, timely visual reha
Externí odkaz:
https://doaj.org/article/2fc5be68d3844c5eba6ea68012cf6f57
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 28, Iss , Pp 101746- (2022)
Purpose: The purpose of this report is to describe a case of a patient with microspherophakia (MSP) who had a scleral rupture during a retinal detachment (RD) repair with primary scleral buckle and cryoretinopexy. Observations: A 48-year-old woman wi
Externí odkaz:
https://doaj.org/article/aec6269025cf452d8800156a876025b7
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 28, Iss , Pp 101723- (2022)
Purpose: To report a case of congenital ciliary body cysts causing microspherophakia, ectopia lentis, and secondary angle closure glaucoma in an infant. Observations: A 16-month-old male was found to have bilateral ciliary body cysts associated with
Externí odkaz:
https://doaj.org/article/5e0b6f2782914286bc1d0bd75f3c31a5