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Oxford University Press Genetic Skin Disorders No.33 - Oxford Medical Genetics Monograph

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Description

Genetic Skin Disorders: No.33 is a comprehensive reference that documents 327 distinct inherited dermatologic conditions in exhaustive detail. Published by Oxford University Press, this scholarly monograph serves medical professionals, researchers, and dermatologists seeking authoritative clinical guidance. Each disease entry presents major and minor dermatologic features, associated clinical abnormalities, histopathology findings including light and electron microscopy analysis, biochemical and molecular data, treatment protocols, inheritance patterns with recurrence risk calculations, prenatal diagnosis options, differential diagnosis guidance, and annotated references. The appendix on Differential Diagnosis by Skin Sign provides rapid clinical lookup for systematic condition identification. This resource combines rigorous scientific documentation with practical diagnostic tools, making it essential for anyone managing patients with genetic skin conditions or conducting dermatologic research.

Key Features

Covers 327 distinct inherited dermatologic conditions with complete clinical descriptions and diagnostic criteria.

Genetic Skin Disorders entries include histopathology sections with both light microscopy and electron microscopy findings.

Oxford Monographs on Medical Genetics provides biochemical and molecular information alongside inheritance patterns and recurrence risks.

Features prenatal diagnosis options and differential diagnosis guidance to support clinical decision-making.

Appendix on Differential Diagnosis by Skin Sign enables rapid identification of conditions based on observable skin presentation.

Annotated references support further research and advanced clinical investigation of genetic dermatologic disorders.

Product Specifications

Format
hardcover
Domain
Amazon UK
Release Date
30 October 1997
Listed Since
14 December 2006

Barcode

No barcode data available

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