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Titlebook: Genetics of Ocular Diseases; H. V. Nema,Nitin Nema Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive license to S

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發(fā)表于 2025-3-21 17:01:27 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Genetics of Ocular Diseases
編輯H. V. Nema,Nitin Nema
視頻videohttp://file.papertrans.cn/383/382741/382741.mp4
概述Includes a separate chapter on genetic counselling in eye diseases with the help of examples.Discusses recent trends in gene therapy of eye diseases.Written by well-known ophthalmologists and genetici
圖書(shū)封面Titlebook: Genetics of Ocular Diseases; H. V. Nema,Nitin Nema Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive license to S
描述.The book focuses on describing the importance of genetics?in eye diseases in a comprehensive and concise manner. Mutations in different set of genes have been detected and incriminated in complex mechanisms of causing leading eye diseases such as cataract and glaucoma. This book written by well-established ophthalmologists and geneticists presents a complicated subject in simple and easy to understand manner. Chapters cover the concept of gene therapy which is an emerging subject with high potential. The book includes a separate chapter on genetic counseling, which has become an integral component of ophthalmology. The book will assist the practicing ophthalmologists in early diagnosis of genetic eye diseases as well as help the geneticists in understaning the basic concepts. It will also be useful for students who are preparing for MD, MS, DNB and FRCS examinations..
出版日期Book 2022
關(guān)鍵詞Genetics of cataract; Genetics of glaucoma; Genetics of retinoblastoma; Genetics of strabismus; Sex-link
版次1
doihttps://doi.org/10.1007/978-981-16-4247-0
isbn_softcover978-981-16-4249-4
isbn_ebook978-981-16-4247-0
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Singapor
The information of publication is updating

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Die Pathologie des Herzstoffwechsels,l scarring. It commonly occurs as an isolated disease but is known to be associated with other ocular and systemic disorders. Genetic component in the etiology of keratoconus is well recognized with contribution from environmental and more recently, inflammatory factors. Multiple approaches have bee
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https://doi.org/10.1007/978-3-531-91867-9Disease (DED). Therefore, the environmental and genetic risk factors for developing DED are multiple and diverse..The spectrum of DED includes both evaporative and aqueous deficient forms, with a combined form predominating in most cases.
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,Die Stabilit?t der Befehlsketten,different routes of administration of gene therapy. Embryology of the lens starts with the neuroectoderm stimulating the thickened surface ectoderm with transcription factors including PAX 6, Sox2, and Six3 gene to form the lens placode. The invagination later leads to the formation of the lens pit
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https://doi.org/10.1007/978-3-658-07758-7e in one’s life. Glaucoma, characterized by progressive damage to retinal ganglion cells (RGCs) and concomitant visual field loss is the leading cause of irreversible blindness globally. People from all the age groups can be affected by the varying glaucoma subtypes with either Mendelian or complex
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