by Alex Levin (Author),‎ Mario Zanolli (Author),‎ Jenina Capasso (Author)

The field of ocular genetics is rapidly advancing, with significant strides being made in gene identification and the understanding of the underlying mechanisms of hereditary eye disease. Inherited eye disorders are one of the leading causes of blindness worldwide, and there is a pressing need for a comprehensive textbook that can provide ophthalmologists and other professionals with a better understanding of these conditions.

The Wills Eye Handbook of Ocular Genetics, authored by Alex Levin, Mario Zanolli, and Jenina Capasso of Wills Eye Hospital, is a practical and reader-friendly guide on the diagnosis and management of ophthalmic genetic conditions. This textbook aims to facilitate optimal patient management and outcomes, equipping practitioners with the knowledge and skills necessary to effectively handle inherited eye diseases.

The book begins each chapter with an overview of a specific disease, followed by an exploration of the relevant modern genetic concepts. The authors outline the pathways to attaining a correct diagnosis and provide insights gained from years of hands-on expertise in the field. At the end of each chapter, readers are presented with questions and answers that allow them to test their knowledge in real-life scenarios they may encounter in their everyday practice.

One of the key features of this handbook is its focus on patient-centered genetic counseling issues. The authors discuss various aspects of genetic counseling, such as reproduction, dealing with emotional reactions, prognosis, and future options. This patient-centered approach ensures that practitioners are well-equipped to address the unique needs and concerns of their patients with genetic eye disorders.

The book covers a wide range of ocular genetic conditions, including anterior segment disorders like corneal dystrophies and aniridia, as well as vitreoretinopathies and retinal diseases such as incontinentia pigmenti, retinitis pigmentosa, Bardet-Biedl syndrome, Stargardt disease, achromatopsia, and juvenile X-linked retinoschisis. This comprehensive coverage allows practitioners in all subspecialties, including ophthalmology and genetics, to navigate the complexities of genetic eye diseases with confidence.

With 296 pages, this eBook digital edition of The Wills Eye Handbook of Ocular Genetics is a valuable resource for practitioners at all levels. It provides a thorough understanding of the fundamentals of ocular genetics, including basic genetics, inheritance patterns, genetic testing, and ethical issues. The language used in the book is easily understandable, making it accessible to a wide range of readers.

The book is published by Thieme, a renowned publisher known for its high-quality medical textbooks. The first edition of The Wills Eye Handbook of Ocular Genetics was released on November 21, 2017, ensuring that the information it contains is up-to-date and in line with the latest advancements in the field of ocular genetics.

What sets this book apart from others in the field is its practical and reader-friendly approach. The authors have taken complex concepts and distilled them into easily understandable information, making this handbook a valuable resource for both seasoned professionals and those new to the field of ocular genetics.

Reading The Wills Eye Handbook of Ocular Genetics will not only deepen your understanding of inherited eye diseases but also equip you with the knowledge and skills needed to effectively manage these conditions. By utilizing the information and insights presented in this handbook, you can ensure that your patients receive optimal care and achieve the best possible outcomes.

If you are an ophthalmologist, geneticist, or a professional who works with patients with genetic eye disorders, ordering a copy of The Wills Eye Handbook of Ocular Genetics is a must. Don’t miss the opportunity to enhance your knowledge and improve your ability to manage inherited eye diseases, ultimately making a positive impact on the lives of your patients.