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Hereditary chorioretinal disorders

Cheung, Gemmy.

Hereditary chorioretinal disorders

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Hereditary chorioretinal disorders/ edited by Gemmy Cheung.
其他作者:	Cheung, Gemmy.
出版者:	Singapore :Springer Singapore : : 2020.,
面頁冊數:	vii, 147 p. :ill., digital ; : 24 cm.;
提要註:	This volume of the retina atlas focuses on hereditary chorioretinal disorders. The topics covered include retinitis pigmentosa, Best disease, congenital X-linked retinoschisis, cone dystrophy, Stargardt's disease, pattern dystrophy, North Carolina macular dystrophy, choroideremia, Mallattia Leventinese, Bietti's crystalline dystrophy, and albinism. All clinical features are clearly illustrated with multimodal imaging techniques. The utility of some of the latest imaging tools such as OCT angiography, adaptive optics-scanning laser ophthalmoscopy, and microperimetery is discussed. Readers will gain valuable new insights into pathogenesis at the molecular level, which have been facilitated by recent genetic discoveries. The use of genetic testing and the latest advances in and challenges of gene therapy and cell-based therapy are also covered in detail. Hereditary Chorioretinal Disorders atlas is one of nine volumes in the series Retina Atlas. The series provides validated and comprehensive information on vitreoretinal diseases, covering imaging basics, retinal vascular diseases, macular disorders, ocular inflammatory and infectious disorders, retinal degeneration, the surgical retina, ocular oncology, pediatric retina and trauma.
Contained By:	Springer eBooks
標題:	Ophthalmology. -
電子資源:	https://doi.org/10.1007/978-981-15-0414-3
ISBN:	9789811504143

Hereditary chorioretinal disorders
Hereditary chorioretinal disorders[electronic resource] /edited by Gemmy Cheung. - Singapore :Springer Singapore :2020. - vii, 147 p. :ill., digital ;24 cm. - Retina Atlas,2662-5741. - Retina Atlas..

Retinits pigmentosa and allied disorders -- Best's disease -- Congenital X-linked retinoschisis -- Progressive cone dystrophy and cone-rod dystrophy -- Pattern dystrophy of the retinal pigment epithelium -- Stargardt's disease and fundus flavimaculatus -- North Carolina macular dystrophy -- Choroideremia -- Malattia Leventinese or Doyne honeycomb retinal dystrophy -- Bietti's crystalline dystrophy -- Albinism.

This volume of the retina atlas focuses on hereditary chorioretinal disorders. The topics covered include retinitis pigmentosa, Best disease, congenital X-linked retinoschisis, cone dystrophy, Stargardt's disease, pattern dystrophy, North Carolina macular dystrophy, choroideremia, Mallattia Leventinese, Bietti's crystalline dystrophy, and albinism. All clinical features are clearly illustrated with multimodal imaging techniques. The utility of some of the latest imaging tools such as OCT angiography, adaptive optics-scanning laser ophthalmoscopy, and microperimetery is discussed. Readers will gain valuable new insights into pathogenesis at the molecular level, which have been facilitated by recent genetic discoveries. The use of genetic testing and the latest advances in and challenges of gene therapy and cell-based therapy are also covered in detail. Hereditary Chorioretinal Disorders atlas is one of nine volumes in the series Retina Atlas. The series provides validated and comprehensive information on vitreoretinal diseases, covering imaging basics, retinal vascular diseases, macular disorders, ocular inflammatory and infectious disorders, retinal degeneration, the surgical retina, ocular oncology, pediatric retina and trauma.

ISBN: 9789811504143

Standard No.: 10.1007/978-981-15-0414-3doiSubjects--Topical Terms:

266457
Ophthalmology.

LC Class. No.: RE551 / .H474 2020

Dewey Class. No.: 617.735

Hereditary chorioretinal disorders
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520 $a This volume of the retina atlas focuses on hereditary chorioretinal disorders. The topics covered include retinitis pigmentosa, Best disease, congenital X-linked retinoschisis, cone dystrophy, Stargardt's disease, pattern dystrophy, North Carolina macular dystrophy, choroideremia, Mallattia Leventinese, Bietti's crystalline dystrophy, and albinism. All clinical features are clearly illustrated with multimodal imaging techniques. The utility of some of the latest imaging tools such as OCT angiography, adaptive optics-scanning laser ophthalmoscopy, and microperimetery is discussed. Readers will gain valuable new insights into pathogenesis at the molecular level, which have been facilitated by recent genetic discoveries. The use of genetic testing and the latest advances in and challenges of gene therapy and cell-based therapy are also covered in detail. Hereditary Chorioretinal Disorders atlas is one of nine volumes in the series Retina Atlas. The series provides validated and comprehensive information on vitreoretinal diseases, covering imaging basics, retinal vascular diseases, macular disorders, ocular inflammatory and infectious disorders, retinal degeneration, the surgical retina, ocular oncology, pediatric retina and trauma.
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