The Chromosome 22q11 2 Deletion Syndrome

  • Publisher : Academic Press
  • File Size : 50,9 Mb
  • Release : 19 August 2022
  • ISBN : 9780128160480
  • Page : 526 pages
  • Rating : 4/5 (21 users)

Summary: The Chromosome 22q11 2 Deletion Syndrome PDF is a Fantastic Medical book by Donna M. McDonald-McGinn. It was published by Academic Press on 19 August 2022. This Book has 526 pages and Available to download in PDF, EPUB and Kindle Format. Read detail book and summary below and click download button to get book file and read directly from your devices.

The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment serves as the first comprehensive, user-friendly resource on the etiology, prognosis, and recurrence risk associated with the chromosome 22q11.2 deletion 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 every applicable subspecialty, such as, cardiology, immunology, endocrinology, gastroenterology, hematology, ophthalmology, neurology, and psychiatry, among other fields. This book presents an authoritative resource with full color images that enhance concept illustration and aid in real-time decision-making. As 22q11.2 deletion syndrome has become a model for understanding rare and frequent anomalies, numerous medical issues, cognitive and behavioral phenotypes, and later onset conditions, this text will become the go to resource for clinicians, researchers, trainees, and motivated family members, in gaining a full understanding of this complex chromosomal disorder. Provides a complete description of 22q11.2 deletion syndrome for healthcare professionals, researchers, trainees, and families affected by this common condition Presents diagnostic and treatment strategies to help tackle this complex and often undiagnosed and therefore undertreated condition Covered in a user-friendly, practical format that emphasizes evidence-based evaluation and treatment derived from the latest clinical experience and research in the field Features leading international contributors in numerous sub-specialties, representing the multisystem nature of this condition Includes full color figures, flow charts, tables, and patient images to guide real-time decision-making

The Chromosome 22q11 2 Deletion Syndrome

The Chromosome 22q11 2 Deletion Syndrome
Author: Donna M. McDonald-McGinn
File Size : 40,9 Mb
Category: Medical

The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment serves as the first comprehensive, user-friendly resource on the etiology, prognosis, and recurrence risk associated with the chromosome 22

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DiGeorge Syndrome New Insights for the Healthcare Professional 2011 Edition

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Category: Medical

DiGeorge Syndrome: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about DiGeorge Syndrome in a compact format. The editors have

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DiGeorge Syndrome New Insights for the Healthcare Professional 2012 Edition

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File Size : 45,9 Mb
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The Development of Cognitive Control and Its Neural Correlates in Children with Chromosome 22q11 2 Deletion Syndrome

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Author: Heather Mehle Shapiro
File Size : 49,9 Mb
Category: Medical

Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is a neurogenetic disorder that is associated with cognitive dysfunction and significantly elevated risk for developing schizophrenia. A better understanding of specific neurocognitive impairments

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File Size : 49,6 Mb
Category: Medical

The 22q11.2 deletion syndrome, also known as velo-cardio-facial syndrome and DiGeorge syndrome, is relatively new. The genetic test to determine if a child has it has only been available since 1994.

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File Size : 53,7 Mb
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File Size : 49,8 Mb
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"22q11.2 deletion syndrome (22q11.2DS) is the most common contiguous gene syndrome and is characterized by a 3 Mb de novo deletion of the chromosome 22q11.2 region in 90% of individuals. Patients

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