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Wills Eye Handbook of Ocular Genetics

Wills Eye Handbook of Ocular Genetics

by Alex V. LevinMario Zanolli and Jenina Capasso
Paperback
Publication Date: 07/02/2018

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Many serious, potentially blinding eye disorders have a genetic basis. Currently, there are relatively few ocular geneticists in the world, yet inherited eye disease is one of the leading causes of blindness worldwide.

Significant strides have been made in gene identification and acquisition of knowledge on the underlying mechanisms of hereditary eye disease. The field of ocular genetics is becoming an increasingly relevant part of ophthalmologists' purview. This has resulted in a dire need for a comprehensive textbook ophthalmologists and other professionals who work with patients with genetic disorders can utilize to gain a better understanding of inherited eye disorders.

The Wills Eye Handbook of Ocular Genetics, by Alex Levin, Mario Zanolli, and Jenina Capasso of Wills Eye Hospital, is a practical, reader-friendly guide on the diagnosis and management of ophthalmic genetic conditions. Every chapter begins with a disease overview, followed by relevant modern genetic concepts, pathways to attaining the correct diagnosis, and pitfalls and pearls gleaned from years of hands-on expertise. At the end of each chapter, questions and answers enable readers to test their knowledge in real-life scenarios they might face in everyday practice. The ultimate goal of this clinically robust handbook is to facilitate optimal patient management and outcomes.

Book Features

  • Fundamentals, including basic genetics, inheritance patterns, genetic testing, and ethical issues
  • Patient-centered genetic counseling issues such as reproduction, dealing with emotional reactions, prognosis, and future options
  • Anterior segment disorders - from corneal dystrophies and aniridia - to childhood cataract and microphthalmia
  • A broad spectrum of vitreoretinopathies and retinal diseases including incontinentia pigmenti, retinitis pigmentosa, Bardet-Biedl syndrome, choroideremia, Stargardt disease, achromatopsia, and juvenile X-linked retinoschisis

This textbook is essential reading for practitioners at all levels and in all subspecialties including ophthalmology and genetics. They will find it an excellent resource for navigating the complexities of genetic eye disease.

ISBN:
9781626232938
9781626232938
Category:
Ophthalmology
Format:
Paperback
Publication Date:
07-02-2018
Language:
English
Publisher:
Thieme Medical Publishers, Incorporated
Country of origin:
United States
Pages:
308
Dimensions (mm):
152x229x17mm
Alex V. Levin

Dr. Alex V. Levin, MD, MHSc, FAAP, FAAO, FRCSC, is the Chief of Pediatric Ophthalmology and Ocular Genetics at Wills Eye Institute and is the Robison D. Harley, MD, Endowed Chair in Pediatric Ophthalmology and Ocular Genetics.

He was the co-founder and co-director of the Ocular Genetics Program at the Toronto Hospital for Sick Children. In 2008, he relocated back to Wills, where he is also Professor of Ophthalmology and Pediatrics at the Sidney Kimmel Medical College of Thomas Jefferson University.

Mario Zanolli

Dr. Mario Zanolli is on staff at Clínica Alemana de Santiago and Hospital de Niños Roberto del Río in Chile. Dr. Zanolli graduated from medical school at Pontificia Universidad Católica de Chile and completed an ophthalmic pediatric residency at Fundación Oftalmológica Los Andes.

He completed an ocular genetics fellowship program at Wills Eye Hospital. Dr. Zanolli is interested in genetic eye disorders and pediatric disorders such as premature retinopathy, retinoblastoma, cataract, glaucoma, and uveítis.

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