£124.97

Brand: Nova Biomedical Books Cystic Fibrosis: Etiology, Diagnosis and Treatments - Nova Books

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Description

Gain a comprehensive understanding of Cystic Fibrosis through this detailed research volume. Also known as CF, mucovoidosis, or mucoviscidosis, this hereditary disease affects the exocrine glands of the lungs, liver, pancreas, and intestines. This book examines how the condition leads to progressive disability through multisystem failure. Readers will learn about the biological impact of abnormally thick mucus and how it contributes to frequent lung infections. The text covers the physiological causes behind poor growth, greasy stools, and fat-soluble vitamin deficiencies resulting from diminished pancreatic enzyme secretion. It also addresses specific reproductive concerns, such as infertility in males due to congenital bilateral absence of the vas deferens. Designed for those studying genetics and medical research, this volume provides essential information on symptoms that often appear in infancy and childhood, including meconium ileus. This resource serves as a valuable guide for understanding the complex etiology and the current landscape of diagnosis and treatment for this multisystem disorder.

Key Features

Covers the fundamental etiology of Cystic Fibrosis and its impact on the exocrine glands in the lungs, liver, pancreas, and intestines.

Explains the physiological mechanisms behind thick mucus production and its role in causing frequent lung infections.

Details the relationship between diminished pancreatic enzyme secretion and symptoms like poor growth and vitamin deficiencies.

Provides information on reproductive health issues, including male infertility caused by the absence of the vas deferens.

Discusses the early onset of symptoms in infancy and childhood, such as meconium ileus.

Serves as a specialized resource for the Genetics-Research and Issues Series regarding multisystem failure.

Product Specifications

Format
hardcover
Domain
Amazon UK
Release Date
01 December 2009
Listed Since
08 May 2009

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