与常染色体隐性遗传性最佳rophin病相关的闭角型青光眼。 - Suppr

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Angle-closure glaucoma associated with autosomal recessive bestrophinopathy.

作者信息

Raja Vidya, Manthravadi Shiva Krishna, Anjanamurthy Rupa

机构信息

Department of Glaucoma Services, Aravind Eye Hospital, Madurai, Tamil Nadu, India.

Department of Adult Strabismus and Pediatric Ophthalmology, Aravind Eye Hospital, Madurai, Tamil Nadu, India.

出版信息

Indian J Ophthalmol. 2022 Jul;70(7):2657-2658. doi: 10.4103/ijo.IJO_2411_21.

DOI:10.4103/ijo.IJO_2411_21

PMID:35791192

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9426077/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9570/9426077/319a5a2ab645/IJO-70-2657-g001.jpg

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Micropulse transscleral cyclophotocoagulation in the treatment of autosomal recessive bestrophinopathy combined with angle closure glaucoma: a case report.

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本文引用的文献

Autosomal recessive bestrophinopathy associated with angle-closure glaucoma.

Doc Ophthalmol. 2014 Aug;129(1):57-63. doi: 10.1007/s10633-014-9444-z. Epub 2014 May 24.

Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.

Ophthalmology. 2013 Apr;120(4):809-20. doi: 10.1016/j.ophtha.2012.09.057. Epub 2013 Jan 3.

Childhood-onset autosomal recessive bestrophinopathy.

Arch Ophthalmol. 2011 Aug;129(8):1088-93. doi: 10.1001/archophthalmol.2011.197.

Autosomal recessive vitelliform macular dystrophy in a large cohort of vitelliform macular dystrophy patients.

Retina. 2011 Mar;31(3):581-95. doi: 10.1097/IAE.0b013e318203ee60.

Bestrophins and retinopathies.

Pflugers Arch. 2010 Jul;460(2):559-69. doi: 10.1007/s00424-010-0821-5. Epub 2010 Mar 28.

Detailed analysis of retinal function and morphology in a patient with autosomal recessive bestrophinopathy (ARB).

Doc Ophthalmol. 2009 Jun;118(3):239-46. doi: 10.1007/s10633-008-9154-5. Epub 2008 Nov 5.

Biallelic mutation of BEST1 causes a distinct retinopathy in humans.

Am J Hum Genet. 2008 Jan;82(1):19-31. doi: 10.1016/j.ajhg.2007.08.004.

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