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Wills Eye Handbook of Ocular Genetics, 1ed

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.

Key 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.

Contents

۱ Basic Genetics
۲ Inheritance Patterns
۳ Genetic Testing
۴ Ethical Issues
۵ Corneal Dystrophies
۶ Aniridia
۷ Peters Anomaly
۸ Axenfeld-Rieger Syndrome
۹ Primary Congenital Glaucoma and Juvenile Open Angle Glaucoma
۱۰ Childhood Cataract
۱۱ Microphthalmia
۱۲ Marfan Syndrome and Other Causes of Ectopia Lentis
۱۳ Familial Exudative Vitreoretinopathy
۱۴ Stickler Syndrome
۱۵ VCAN Vitreoretinopathies (Erosive Vitreoretinopathy and Wagner Syndrome)
۱۶ Incontinentia Pigmenti
۱۷ Retinitis Pigmentosa
۱۸ Usher Syndrome
۱۹ Bardet-Biedl Syndrome
۲۰ Cone-Rod Dystrophy
۲۱ Choroideremia
۲۲ Enhanced S-Cone Syndrome and Other NR2E3-Related Retinal Dystrophies
۲۳ Stargardt Disease and Other ABCA4 Retinopathies
۲۴ Best Vitelliform Macular Dystrophy (Best Disease)
۲۵ Leber Congenital Amaurosis
۲۶ Achromatopsia
۲۷ Congenital Stationary Night Blindness
۲۸ Juvenile X-Linked Retinoschisis
۲۹ Retinoblastoma
۳۰ Optic Nerve Hypoplasia
۳۱ Leber Hereditary Optic Neuropathy
۳۲ Complex Ocular Disorders
۳۳ Albinism

قیمت : 5000 تومان

لینک کوتاه : https://bookbaz.ir/?p=105472
نویسنده : Alex Levin , Mario Zanolli
ناشر : Thieme; 1 edition
سال انتشار : 2018
زبان کتاب : انگلیسی
نوع فایل : PDF
تعداد صفحات : 310
(ISBN) شابک : 9781626232938
قیمت کتاب درآمازون : $81.18
حجم فایل : 12 MB

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