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Author: Javier Publisher: ISBN: Category : Languages : en Pages : 0
Book Description
In the fascinating world of ophthalmology, understanding genetic inheritance patterns is crucial for unraveling the mysteries of vision. In this subchapter, we will delve into the intricate mechanisms that govern the transmission of genes related to eye diseases and traits. By comprehending these patterns, students like you can gain a deeper understanding of how genetics influences ophthalmic conditions, paving the way for future breakthroughs in this field. One of the fundamental concepts in genetic inheritance is the distinction between dominant and recessive traits. Dominant traits are those that are expressed even if an individual carries only one copy of the gene responsible for that trait. On the other hand, recessive traits require two copies of the gene to be present for the trait to manifest. Understanding this distinction helps us predict the likelihood of certain eye diseases and traits appearing in individuals and their offspring. Another critical aspect of genetic inheritance is the concept of genetic carriers. Carriers are individuals who possess a recessive gene for a particular trait but do not exhibit any symptoms themselves. This is particularly relevant in ophthalmology, as carriers can unknowingly pass on these genes to their children. By understanding carrier status and inheritance patterns, we can identify individuals who may carry a genetic predisposition to certain eye diseases. Inheritance patterns in ophthalmology can also be influenced by gender. For instance, X-linked inheritance is a pattern in which genes located on the X chromosome are primarily responsible for the development of certain eye conditions. Since males have one X and one Y chromosome, they are more susceptible to X-linked diseases. Females, on the other hand, have two X chromosomes, providing some level of protection against X-linked conditions. Furthermore, genetic inheritance patterns can be further complicated by the phenomenon of genetic mutations. Mutations can occur spontaneously or be inherited from parents and can alter the function of certain genes, leading to the development of eye diseases. By studying these mutations, scientists can gain insights into the underlying causes of these conditions and potentially develop targeted treatments.
Author: Gyan Prakash Publisher: Springer Nature ISBN: 9811591849 Category : Medical Languages : en Pages : 478
Book Description
This third volume, with three supporting editors, broadens its focus on genetic eye research from the Asian to the global scale. New efforts and a new awareness have sparked important discussions on genetic eye research, and new plans are being implemented to identify the genes responsible for numerous eye diseases. The book introduces the latest findings on genetics in eye diseases, gene therapy, and genome-wide association analysis, and the efforts of the Global Eye Genetic Consortium (GEGC). The book’s editors have been instrumental in developing strategies for discovering the new genes involved in many eye diseases. All chapters were written by leading researchers working on eye genetics from the fields of Human Genetics, Ophthalmology, Molecular Biology, Biochemistry, Sensory Sciences, and Clinical Research. Advances in Vision Research, Volume III is a major resource for all researchers, clinicians, clinical researchers, and allied eye health professionals with an interest in eye diseases around the globe.
Author: Gyan Prakash Publisher: Springer ISBN: 9811308845 Category : Medical Languages : en Pages : 464
Book Description
This second volume continues with a focus on the state of the art in genetic eye research in Asia and the Pacific. Though there has been an explosion of information on genetic eye research in western countries, more than sixty percent of the human genes involved in eye diseases in the Asian and Pacific population remain unknown. However, new efforts and a new awareness have sparked important discussions on the subject, and new plans are being implemented to discover the genes responsible for many eye diseases in the population. The book reviews the latest findings; its content ranges from genetic aspects of human migration to DNA sequence analysis, genome-wide association analysis, and disease phenotypes. The efforts of the Asian Eye Genetic Consortium (AEGC) are also discussed. The book’s editors have been instrumental in developing strategies for discovering the new Asian genes involved in many eye diseases. All chapters were written by leading researchers working on Asian eye genetics from the fields of Human Genetics, Ophthalmology, Molecular Biology, Biochemistry, Sensory Sciences, and Clinical Research. Advances in Vision Research, Volume II will prove to be a major resource for all researchers, clinicians, clinical researchers, and allied eye health professionals with an interest in eye diseases among the Asian population.
Author: Gyan Prakash Publisher: Springer ISBN: 4431565116 Category : Medical Languages : en Pages : 519
Book Description
This book presents the state of the art in genetic eye research in Asia and the Pacific. Though there has been an explosion of information on genetic eye research in western countries, more than sixty percent of the human genes involved in eye diseases in the Asian and Pacific population remain unknown. However, new efforts and a new awareness have sparked important discussions on the subject, and new plans are being implemented to discover the genes responsible for many eye diseases in the population. The book reviews the latest findings; its content ranges from genetic aspects of human migration to DNA sequence analysis, genome-wide association analysis, and disease phenotypes. The efforts of the Asian Eye Genetic Consortium (AEGC) are also discussed. The book’s editors have been instrumental in developing strategies for discovering the new Asian genes involved in many eye diseases. All chapters were written by leading researchers working on Asian eye genetics from the fields of Human Genetics, Ophthalmology, Molecular Biology, Biochemistry, Sensory Sciences, and Clinical Research. Advances in Vision Research, Volume I will prove to be a major resource for all researchers, clinicians, clinical researchers, and allied eye health professionals with an interest in eye diseases among the Asian population.
Author: National Academies of Sciences, Engineering, and Medicine Publisher: National Academies Press ISBN: 0309439981 Category : Medical Languages : en Pages : 587
Book Description
The ability to see deeply affects how human beings perceive and interpret the world around them. For most people, eyesight is part of everyday communication, social activities, educational and professional pursuits, the care of others, and the maintenance of personal health, independence, and mobility. Functioning eyes and vision system can reduce an adult's risk of chronic health conditions, death, falls and injuries, social isolation, depression, and other psychological problems. In children, properly maintained eye and vision health contributes to a child's social development, academic achievement, and better health across the lifespan. The public generally recognizes its reliance on sight and fears its loss, but emphasis on eye and vision health, in general, has not been integrated into daily life to the same extent as other health promotion activities, such as teeth brushing; hand washing; physical and mental exercise; and various injury prevention behaviors. A larger population health approach is needed to engage a wide range of stakeholders in coordinated efforts that can sustain the scope of behavior change. The shaping of socioeconomic environments can eventually lead to new social norms that promote eye and vision health. Making Eye Health a Population Health Imperative: Vision for Tomorrow proposes a new population-centered framework to guide action and coordination among various, and sometimes competing, stakeholders in pursuit of improved eye and vision health and health equity in the United States. Building on the momentum of previous public health efforts, this report also introduces a model for action that highlights different levels of prevention activities across a range of stakeholders and provides specific examples of how population health strategies can be translated into cohesive areas for action at federal, state, and local levels.
Author: B. Wissinger Publisher: Karger Medical and Scientific Publishers ISBN: 3805575785 Category : Medical Languages : en Pages : 230
Book Description
The objective of this publication is to enhance mutual understanding and communication between ophthalmologists, molecular geneticists, genetic counselors and biomedical researchers. In the introductory chapter, current genetic paradigms and experimental genetic approaches relevant to the nature of hereditary disorders are discussed. The following contribution on the epidemiology of hereditary ocular disorders provides an excellent reference to geneticists as well as clinicians. Myopia is presented as an example of a complex clinical phenotype where genes and environment interact. Further molecular ophthalmogenetic topics, such as corneal dystrophies, cataract, glaucoma, opticus neuropathy, non-syndromic and syndromic pigmentary retinopathies, defects of vitamin A metabolism and macular dystrophies including age-related macular degeneration, are investigated in depth. The volume concludes with a survey of color vision deficiencies, a discussion of animal models and gene therapy, and a useful description of technical devices supporting patients who are losing sight.
Author: Elias I. Traboulsi Publisher: OUP USA ISBN: 0195326148 Category : Medical Languages : en Pages : 940
Book Description
This book takes a clinical approach to the patient with a genetic disease that affects the eye. The chapters on particular types of diseases follow the same organizational format, covering history, pathogenesis and etiology, epidemiology, classification, clinical manifestations and diagnosis, and treatment. The recent progress achieved in the molecular genetics of eye disease is fully reflected throughout the book. It is written by leading experts in the field and provides clinical, molecular genetic and management information on common and rare diseases. The chapters are heavily illustrated and provide a good Atlas for the practicing ophthalmologist or geneticist.
Author: Karl R. Gegenfurtner
Author: Karl R. Gegenfurtner
Author: Javier
Author: Gyan Prakash
Author: Gyan Prakash
Author: Rajendranath Pepe Ramnath
Author: Gyan Prakash
Author: National Academies of Sciences, Engineering, and Medicine
Author: B. Wissinger
Author: John D. Hawkins
Author: Elias I. Traboulsi