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The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment serves as the first comprehensive, user-friendly resource on the etiology,… Read more
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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.
Pediatric and adult healthcare providers who deliver treatment for individuals affected by chromosome 22q11.2 deletion syndrome including primary care providers, geneticists and genetic counselors, cardiologists, dentists, developmental pediatricians, endocrinologists, ENTs, gastroenterologists, general surgeons, hematologists, immunologists, neurologists, ophthalmologists, orthopedists, plastic surgeons, psychiatrists, urologists, educators, undergraduate and graduate students, psychologists and social workers, and therapists of all types including occupational, physical, speech, and behavioral therapists, as well as interested family members.
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