£122.99

Retinitis Pigmentosa: Causes, Diagnosis and Treatment Book

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Description

Gain a comprehensive understanding of Retinitis Pigmentosa (RP) with this specialized medical text. This book explores the group of progressive hereditary retinal diseases that lead to the degeneration of rod and cone photoreceptors. As one of the leading causes of hereditary blindness in the developed world, RP presents significant challenges for patients and medical professionals alike. This resource covers essential clinical symptoms such as nyctalopia, progressive visual field loss, and the deterioration of visual acuity during adolescence. It provides detailed information on how the condition affects one in 3000-5000 individuals and examines the role of mutations in more than 40 different genes. Whether you are studying nonsyndromic RP or its presence within neurological or systemic disorders like Usher's syndrome, this volume offers vital research developments in eye and vision science.

Key Features

Covers the primary causes of Retinitis Pigmentosa, including mutations found in more than 40 different genes.

Details clinical symptoms such as nyctalopia and the progressive loss of visual field and acuity.

Explores the distinction between nonsyndromic RP and cases linked to systemic disorders like Usher's syndrome.

Provides essential research developments regarding the degeneration of rod and cone photoreceptors.

Offers professional insights into a condition affecting up to one in 3000-5000 individuals.

Product Specifications

Format
paperback
Domain
Amazon UK
Release Date
01 July 2010
Listed Since
13 November 2009

Barcode

No barcode data available

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