Wills Eye Handbook of Ocular Genetics
eBook - PDF

Wills Eye Handbook of Ocular Genetics

  1. 307 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Wills Eye Handbook of Ocular Genetics

Book details
Table of contents
Citations

About This Book

Highly Commended by the BMA Medical Book Awards for Surgical Specialties!

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.

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Yes, you can access Wills Eye Handbook of Ocular Genetics by Alex V. Levin, Mario Zanolli, Jenina Capasso in PDF and/or ePUB format, as well as other popular books in Medicine & Opthalmology & Optometry. We have over one million books available in our catalogue for you to explore.

Information

Publisher
Thieme
Year
2016
ISBN
9781626232945

Table of contents

  1. The Wills Eye Handbook of Ocular Genetics
  2. Title Page
  3. Copyright
  4. Dedication
  5. Contents
  6. Preface
  7. Contributors
  8. 1 Basic Genetics
  9. 2 Inheritance Patterns
  10. 3 Genetic Testing
  11. 4 Ethical Issues
  12. 5 Corneal Dystrophies
  13. 6 Aniridia
  14. 7 Peters Anomaly
  15. 8 Axenfeld–Rieger Syndrome
  16. 9 Primary Congenital Glaucoma and Juvenile Open Angle Glaucoma
  17. 10 Childhood Cataract
  18. 11 Microphthalmia
  19. 12 Marfan Syndrome and Other Causes of Ectopia Lentis
  20. 13 Familial Exudative Vitreoretinopathy
  21. 14 Stickler Syndrome
  22. 15 VCAN Vitreoretinopathies (Erosive Vitreoretinopathy and Wagner Syndrome)
  23. 16 Incontinentia Pigmenti
  24. 17 Retinitis Pigmentosa
  25. 18 Usher Syndrome
  26. 19 Bardet–Biedl Syndrome
  27. 20 Cone–Rod Dystrophy
  28. 21 Choroideremia
  29. 22 Enhanced S-Cone Syndrome and Other NR2E3-Related Retinal Dystrophies
  30. 23 Stargardt Disease and Other ABCA4 Retinopathies
  31. 24 Best Vitelliform Macular Dystrophy (Best Disease)
  32. 25 Leber Congenital Amaurosis
  33. 26 Achromatopsia
  34. 27 Congenital Stationary Night Blindness
  35. 28 Juvenile X-Linked Retinoschisis
  36. 29 Retinoblastoma
  37. 30 Optic Nerve Hypoplasia
  38. 31 Leber Hereditary Optic Neuropathy
  39. 32 Complex Ocular Disorders
  40. 33 Albinism
  41. Index