一名年轻男性患黄斑营养不良，其姐妹中有患角膜营养不良者。 - Suppr

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超能文献

Macular dystrophy in a young male with corneal dystrophy among sisters.

作者信息

Zachariah George, Idiculla Thara, Keshav B R, Nasser Mahmood

机构信息

Department of Ophthalmology, Sur Hospital, Oman.

出版信息

Oman J Ophthalmol. 2011 May;4(2):95-6. doi: 10.4103/0974-620X.83664.

DOI:10.4103/0974-620X.83664

PMID:21897629

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3160080/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8377/3160080/f16db3451398/OJO-4-95-g001.jpg

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本文引用的文献

Stargardt's disease and retinitis pigmentosa: different phenotypic presentations in the same family.斯塔加特病和色素性视网膜炎：同一家族中的不同表型表现。

Eye (Lond). 2005 Nov;19(11):1222-5. doi: 10.1038/sj.eye.6701730.

Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa.三个表现出斯塔加特病与视锥视杆营养不良或色素性视网膜炎组合症状的家族。

Ophthalmology. 2004 Mar;111(3):546-53. doi: 10.1016/j.ophtha.2003.06.010.

Long-term follow-up of Stargardt's disease and fundus flavimaculatus.Stargardt病和黄斑黄素沉着症的长期随访

Ophthalmology. 1998 Mar;105(3):448-57; discussion 457-8. doi: 10.1016/S0161-6420(98)93026-3.

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.一种光感受器细胞特异性ATP结合转运蛋白基因（ABCR）在隐性Stargardt黄斑营养不良中发生突变。

Nat Genet. 1997 Mar;15(3):236-46. doi: 10.1038/ng0397-236.

Asymmetric fundus flavimaculatus/Stargardt's disease, associated with unilateral myopia.

Int Ophthalmol. 1995;19(4):253-5. doi: 10.1007/BF00132695.

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