The Wills Eye Handbook of Ocular Genetics

Alex V. Levin, Mario Zanolli, Jenina E. Capasso (Autoren)

Buch | Softcover

307 Seiten

2018
Thieme Medical Publishers (Verlag)
978-1-62623-293-8 (ISBN)

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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.

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.

1 Basic Genetics

2 Inheritance Patterns

3 Genetic Testing

4 Ethical Issues

5 Corneal Dystrophies

6 Aniridia

7 Peters Anomaly

8 Axenfeld–Rieger Syndrome

9 Primary Congenital Glaucoma and Juvenile Open Angle Glaucoma

10 Childhood Cataract

11 Microphthalmia

12 Marfan Syndrome and Other Causes of Ectopia Lentis

13 Familial Exudative Vitreoretinopathy

14 Stickler Syndrome

15 VCAN Vitreoretinopathies (Erosive Vitreoretinopathy and Wagner Syndrome)

16 Incontinentia Pigmenti

17 Retinitis Pigmentosa

18 Usher Syndrome

19 Bardet–Biedl Syndrome

20 Cone–Rod Dystrophy

21 Choroideremia

22 Enhanced S-Cone Syndrome and Other NR2E3-Related Retinal Dystrophies

23 Stargardt Disease and Other ABCA4 Retinopathies

24 Best Vitelliform Macular Dystrophy (Best Disease)

25 Leber Congenital Amaurosis

26 Achromatopsia

27 Congenital Stationary Night Blindness

28 Juvenile X-Linked Retinoschisis

29 Retinoblastoma

30 Optic Nerve Hypoplasia

31 Leber Hereditary Optic Neuropathy

32 Complex Ocular Disorders

33 Albinism

Erscheinungsdatum	24.01.2018
Zusatzinfo	64 Abb.
Verlagsort	New York
Sprache	englisch
Gewicht	1 g
Einbandart	kartoniert
Themenwelt	Medizin / Pharmazie ► Medizinische Fachgebiete ► Augenheilkunde
Schlagworte	Augenerkrankungen • Augenheilkunde • Erblindung • Genetics • Levin • Ocular • Ophthalmologie
ISBN-10	1-62623-293-8 / 1626232938
ISBN-13	978-1-62623-293-8 / 9781626232938
Zustand	Neuware