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眼皮肤白化病中的黄斑无血管区。

Foveal avascular zone in oculocutaneous albinism.

作者信息

Mansour Hana A, Uwaydat Sami, Yunis Muhamad H, Mansour Ahmad M

机构信息

Ophthalmology, American University of Beirut Faculty of Medicine, Beirut, Lebanon.

Department of Ophthalmology, University of Arkansas for Medical Sciences College of Medicine, Little Rock, Arkansas, USA.

出版信息

BMJ Case Rep. 2021 May 4;14(5):e240208. doi: 10.1136/bcr-2020-240208.

Abstract

Optical coherence tomography angiography imaging in two patients with oculocutaneous albinism, one with severe nystagmus, showed persistence of both the superficial and the deep retinal capillary plexus adding another vascular feature to the foveal hypoplasia.

摘要

两名患有眼皮肤白化病的患者(其中一名患有严重眼球震颤)的光学相干断层扫描血管造影成像显示,视网膜浅层和深层毛细血管丛持续存在,这为黄斑发育不全增加了另一个血管特征。

相似文献

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Foveal avascular zone in oculocutaneous albinism.眼皮肤白化病中的黄斑无血管区。
BMJ Case Rep. 2021 May 4;14(5):e240208. doi: 10.1136/bcr-2020-240208.
2
Optical coherence tomography angiography of foveal hypoplasia.黄斑发育不全的光学相干断层扫描血管造影
Br J Ophthalmol. 2017 Jul;101(7):985-988. doi: 10.1136/bjophthalmol-2016-309200. Epub 2016 Nov 29.
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Nystagmus and Foveal Hypoplasia in a Carrier of Oculocutaneous Albinism.眼球震颤和黄斑发育不良患者为眼皮肤白化病的携带者。
Ophthalmic Surg Lasers Imaging Retina. 2024 Jun;55(6):349-353. doi: 10.3928/23258160-20240207-03. Epub 2024 Jun 1.

本文引用的文献

1
Foveal hypoplasia and optical coherence tomographic imaging.黄斑发育不全与光学相干断层扫描成像
Taiwan J Ophthalmol. 2018 Oct-Dec;8(4):181-188. doi: 10.4103/tjo.tjo_101_18.
2
Multimodal imaging in a patient with Prader-Willi syndrome.普拉德-威利综合征患者的多模态成像
Int J Retina Vitreous. 2018 Nov 30;4:45. doi: 10.1186/s40942-018-0147-6. eCollection 2018.
7
Optical coherence tomography angiography of foveal hypoplasia.黄斑发育不全的光学相干断层扫描血管造影
Br J Ophthalmol. 2017 Jul;101(7):985-988. doi: 10.1136/bjophthalmol-2016-309200. Epub 2016 Nov 29.
8
Clinical Insights Into Foveal Morphology in Albinism.白化病中黄斑形态的临床见解
J Pediatr Ophthalmol Strabismus. 2015 May-Jun;52(3):167-72. doi: 10.3928/01913913-20150427-06.
9
Oculocutaneous albinism.眼皮肤白化病
Orphanet J Rare Dis. 2007 Nov 2;2:43. doi: 10.1186/1750-1172-2-43.

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