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Wills Eye Handbook of Ocular Genetics

Af: Mario Zanolli, Alex V. Levin, Jenina Capasso Engelsk Paperback

Wills Eye Handbook of Ocular Genetics

Af: Mario Zanolli, Alex V. Levin, Jenina Capasso Engelsk Paperback
Tjek vores konkurrenters priser

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.

Tjek vores konkurrenters priser
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Tjek vores konkurrenters priser

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.

Se mere i:
Produktdetaljer
Sprog: Engelsk
Sider: 308
ISBN-13: 9781626232938
Indbinding: Paperback
Udgave:
ISBN-10: 1626232938
Kategori: Oftalmologi
Udg. Dato: 24 jan 2018
Længde: 17mm
Bredde: 230mm
Højde: 153mm
Forlag: Thieme Medical Publishers Inc
Oplagsdato: 24 jan 2018
Forfatter(e) Mario Zanolli, Alex V. Levin, Jenina Capasso


Kategori Oftalmologi


ISBN-13 9781626232938


Sprog Engelsk


Indbinding Paperback


Sider 308


Udgave


Længde 17mm


Bredde 230mm


Højde 153mm


Udg. Dato 24 jan 2018


Oplagsdato 24 jan 2018


Forlag Thieme Medical Publishers Inc