Ankündigung Erscheint vsl. November 2020 Abbildung von McDonald-McGinn | The Chromosome 22q11.2 Deletion Syndrome | 2020 | A Multidisciplinary Approach t...

McDonald-McGinn

The Chromosome 22q11.2 Deletion Syndrome

A Multidisciplinary Approach to Diagnosis and Treatment

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ca. 140,17 €

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2020. Buch. 424 S. Softcover

William Andrew Publishing. ISBN 978-0-12-816047-3

Format (B x L): 19,1 x 23,5 cm

In englischer Sprache

Produktbeschreibung

The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment serves as the first comprehensive, user-friendly resource on the diagnosis, treatment and patient aspects of this syndrome. Leading international contributors cover the background, genetics, testing methods and pathophysiology of 22q11.2DS, placing emphasis on a strong foundation for multidisciplinary treatment strategies. Written by specialists in cardiology, immunology, endocrinology, gastroenterology, hematology, ophthalmology and neurology, among other fields, this book presents an authoritative resource with full color figures, flow charts and tables that enhance concept illustration and aid in real-time decision-making.

As 22q11.2DS has become a model for understanding rare and frequent congenital anomalies, this book will help researchers, clinicians and advanced students gain a full understanding of how to diagnosis and treat rare genetic diseases.



- Provides a comprehensive description of 22q11.2DS syndrome for healthcare professionals, researchers and students
- Presents diagnostic and treatment strategies to help tackle this complex and often misdiagnosed and undertreated syndrome
- Covered in a user-friendly, practical format that emphasizes evidence-based evaluation and treatment derived from the latest research in the field
- Features leading international contributors in various sub-specialties, representing the many body systems affected by this syndrome
- Includes full color figures, flow charts and tables to guide real-time decision-making

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