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Titlebook: Retinal Dystrophy Gene Atlas; Sarwar Zahid,Kari Branham,Thiran Jayasundera Book 2018 Springer International Publishing AG, part of Springe

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发表于 2025-3-21 18:34:56 | 显示全部楼层 |阅读模式
书目名称Retinal Dystrophy Gene Atlas
编辑Sarwar Zahid,Kari Branham,Thiran Jayasundera
视频video
概述Describes a gene and all its possible clinical phenotypes and patient characteristics, along with retinal photos depicting each possible phenotype.Written by prominent retinal dystrophy specialists fr
图书封面Titlebook: Retinal Dystrophy Gene Atlas;  Sarwar Zahid,Kari Branham,Thiran Jayasundera Book 2018 Springer International Publishing AG, part of Springe
描述Classically, photo atlases of retinal dystrophies have been divided into sections that describe and depict a particular retinal finding or disease, after which a differential diagnosis of potential diseases or mutated genes is provided. However, given the rapid improvement in molecular diagnostics, and the exponential increase in our understanding of the phenotypes caused by each mutated gene, the paradigm has changed. Physicians are now more interested in the variable expressivity associated with mutations in each individual gene. Therefore, .Retinal Dystrophy Gene .Atlas .catalogs the different phenotypes that have been reported with each mutated gene. Each section describes a gene and its known clinical phenotypes and features of disease, along with retinal photos of affected patients. Written by prominent retinal dystrophy specialists from the largest dystrophy centers worldwide, .Retinal Dystrophy .Gene Atlas .contains more than 80 chapters, each of which describes the clinical and photographic manifestations of a specific gene. The chapters include stunning clinical color photographs of the retina, autofluorescence imaging, electrophysiologic findings, and cross-sectional ima
出版日期Book 2018
关键词Autosomal Dominant Inheritance; Autosomal Recessive Inheritance; Linked Inheritance; Retinal Dystrophy;
版次1
doihttps://doi.org/10.1007/978-3-319-10867-4
isbn_softcover978-3-030-13234-7
isbn_ebook978-3-319-10867-4
copyrightSpringer International Publishing AG, part of Springer Nature 2018
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发表于 2025-3-21 22:45:16 | 显示全部楼层
,,eveloping and adult photoreceptor layer. It has also been shown to affect photoreceptor function as well as signal transduction through its mediation of cone PDE6 and RetGC1, respectively [1]. Mutations in . cause recessive Leber congenital amaurosis (LCA) and juvenile-onset rod-cone dystrophy, dominant cone-rod dystrophy has also been reported.
发表于 2025-3-22 01:41:30 | 显示全部楼层
,,ponsible for rod-cone (86.9%) and cone-rod (13.1%) dystrophies [2] and for syndromic features associated with Bardet-Biedl syndrome (BBS). . mutations may also cause isolated retinitis pigmentosa (RP) [3, 4].
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,,kely function in membrane trafficking to the primary cilium [1, 2]. Mutations are responsible for rod-cone (86.9%) and cone-rod (13.1%) dystrophies [3] and for syndromic features associated with Bardet-Biedl Syndrome.
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发表于 2025-3-23 05:00:45 | 显示全部楼层
https://doi.org/10.1007/978-3-319-10867-4Autosomal Dominant Inheritance; Autosomal Recessive Inheritance; Linked Inheritance; Retinal Dystrophy;
发表于 2025-3-23 07:22:09 | 显示全部楼层
978-3-030-13234-7Springer International Publishing AG, part of Springer Nature 2018
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