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    1. Medicin
    2. Klinisk medicin och internmedicin
    3. Oftalmologi

    Wills Eye Handbook of Ocular Genetics

    AvAlex V. Levin,Mario Zanolli

    Häftad, Engelska, 2018

    1 205 kr

    Beställningsvara. Skickas inom 5-8 vardagar. Fri frakt över 249 kr.

    Beskrivning

    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 issuesPatient-centered genetic counseling issues such as reproduction, dealing with emotional reactions, prognosis, and future optionsAnterior segment disorders - from corneal dystrophies and aniridia - to childhood cataract and microphthalmiaA broad spectrum of vitreoretinopathies and retinal diseases including incontinentia pigmenti, retinitis pigmentosa, Bardet-Biedl syndrome, choroideremia, Stargardt disease, achromatopsia, and juvenile X-linked retinoschisisThis 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.

    Produktinformation

    • Utgivningsdatum:2018-01-24
    • Mått:152 x 229 x 17 mm
    • Vikt:544 g
    • Format:Häftad
    • Språk:Engelska
    • Antal sidor:308
    • Förlag:Thieme Medical Publishers Inc
    • ISBN:9781626232938

    Utforska kategorier

    • Oftalmologi inom Medicin

    Innehållsförteckning

    • 1 Basic Genetics2 Inheritance Patterns3 Genetic Testing4 Ethical Issues5 Corneal Dystrophies6 Aniridia7 Peters Anomaly8 Axenfeld–Rieger Syndrome9 Primary Congenital Glaucoma and Juvenile Open Angle Glaucoma10 Childhood Cataract11 Microphthalmia12 Marfan Syndrome and Other Causes of Ectopia Lentis13 Familial Exudative Vitreoretinopathy14 Stickler Syndrome15 VCAN Vitreoretinopathies (Erosive Vitreoretinopathy and Wagner Syndrome)16 Incontinentia Pigmenti17 Retinitis Pigmentosa18 Usher Syndrome19 Bardet–Biedl Syndrome20 Cone–Rod Dystrophy21 Choroideremia22 Enhanced S-Cone Syndrome and Other NR2E3-Related Retinal Dystrophies23 Stargardt Disease and Other ABCA4 Retinopathies24 Best Vitelliform Macular Dystrophy (Best Disease)25 Leber Congenital Amaurosis26 Achromatopsia27 Congenital Stationary Night Blindness28 Juvenile X-Linked Retinoschisis29 Retinoblastoma30 Optic Nerve Hypoplasia31 Leber Hereditary Optic Neuropathy32 Complex Ocular Disorders33 Albinism