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
Sprache
Verlagsort
Verlagsgruppe
Elsevier Science & Techn.
Dateigröße
ISBN-13
978-0-12-816048-0 (9780128160480)
Schweitzer Klassifikation
1. 22q11.2 deletion syndrome: Setting the stage2. Genetics, mechanism, and pathophysiology of 22q11.2 deletion syndrome3. Embryonic development in 22q11.2 deletion syndrome4. Congenital heart disease and cardiovascular abnormalities associated with 22q11.2 deletion syndrome 5. The immune system in 22q11.2 deletion syndrome6. Craniofacial abnormalities in association with 22q11.2 deletion syndrome7. Otolaryngologic issues in association with 22q11.2 deletion syndrome8. Endocrine features of 22q11.2 deletion syndrome9. Gastroenterological manifestations associated with 22q11.2 deletion syndrome10. Genitourinary abnormalities in association with 22q11.2 deletion syndrome11. Hematologic and oncological manifestations of 22q11.2 deletion syndrome12. Skeletal anomalies associated with 22q11.2 deletion syndrome13. Ocular findings in 22q11.2 deletion syndrome14. Neurological features associated with 22q11.2 deletion syndrome15. Neurodevelopmental outcome, developmental trajectories, and management in 22q11.2 deletion syndrome16. Speech and language manifestations in 22q11.2 deletion syndrome17. Psychiatric profile in children and youth with 22q11.2 deletion syndrome 18. Mental health in adults with 22q11.2 deletion syndrome19. Primary pediatric care for children and youth with 22q11.2 deletion syndrome20. Healthcare transitions for adolescents and adults with 22q11.2 deletion syndrome21. Reproduction, prenatal screening, and diagnosis in 22q11.2 deletion syndrome22. Quality of life: Educational, vocational, and life planning for individuals with 22q11.2 deletion syndrome23. 22q11.2 deletion syndrome: Future directions 24. General management principles for 22q11.2 deletion syndrome 25. Medical needs associated with 22q11.2 deletion syndrome
