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By Alex Levin, Mario Zanolli, and Jenina Capasso
Introduction: Inherited eye diseases are a leading cause of blindness worldwide. As a result, there is a growing need for ophthalmologists and other professionals to understand and manage genetic eye disorders effectively. The Wills Eye Handbook of Ocular Genetics provides a practical, reader-friendly guide on the diagnosis and management of ophthalmic genetic conditions.
Fundamentals: The handbook covers the basics of genetics, inheritance patterns, genetic testing, and ethical issues related to genetic counseling.
Anterior Segment Disorders: It includes comprehensive information on corneal dystrophies, aniridia, childhood cataract, and microphthalmia.
Vitreoretinopathies and Retinal Diseases: The book offers in-depth insights into incontinentia pigmenti, retinitis pigmentosa, Bardet-Biedl syndrome, choroideremia, Stargardt disease, achromatopsia, and juvenile X-linked retinoschisis.
The Wills Eye Handbook of Ocular Genetics is an essential resource for practitioners at all levels and in all subspecialties, including ophthalmology and genetics. It provides a comprehensive understanding of genetic eye diseases, enabling healthcare professionals to navigate the complexities of genetic eye disease and deliver optimal patient management and outcomes.
Product Details: Paperback: 296 pages, Publisher: Thieme, 1 edition (November 21, 2017), Language: English, ISBN-10: 1626232938, ISBN-13: 978-1626232938, Product Dimensions: 6.2 x 0.5 x 9.2 inches
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