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  • The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment

    The Chromosome 22q11.2 Deletion Syndrome by McDonald-McGinn, Donna M.;

    A Multidisciplinary Approach to Diagnosis and Treatment

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      • Publisher's listprice EUR 132.00
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        51 559 Ft (49 104 Ft + 5% VAT)
      • Discount 10% (cc. 5 156 Ft off)
      • Discounted price 46 403 Ft (44 194 Ft + 5% VAT)

    51 559 Ft

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    Product details:

    • Publisher Elsevier Science
    • Date of Publication 24 August 2022

    • ISBN 9780128160473
    • Binding Paperback
    • No. of pages524 pages
    • Size 234x190 mm
    • Weight 1040 g
    • Language English
    • 215

    Categories

    Long description:

    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.

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    Table of Contents:

    1. 22q11.2 deletion syndrome: Setting the stage
    2. Genetics, mechanism, and pathophysiology of 22q11.2 deletion syndrome
    3. Embryonic development in 22q11.2 deletion syndrome
    4. Congenital heart disease and cardiovascular abnormalities associated with 22q11.2 deletion syndrome
    5. The immune system in 22q11.2 deletion syndrome
    6. Craniofacial abnormalities in association with 22q11.2 deletion syndrome
    7. Otolaryngologic issues in association with 22q11.2 deletion syndrome
    8. Endocrine features of 22q11.2 deletion syndrome
    9. Gastroenterological manifestations associated with 22q11.2 deletion syndrome
    10. Genitourinary abnormalities in association with 22q11.2 deletion syndrome
    11. Hematologic and oncological manifestations of 22q11.2 deletion syndrome
    12. Skeletal anomalies associated with 22q11.2 deletion syndrome
    13. Ocular findings in 22q11.2 deletion syndrome
    14. Neurological features associated with 22q11.2 deletion syndrome
    15. Neurodevelopmental outcome, developmental trajectories, and management in 22q11.2 deletion syndrome
    16. Speech and language manifestations in 22q11.2 deletion syndrome
    17. Psychiatric profile in children and youth with 22q11.2 deletion syndrome
    18. Mental health in adults with 22q11.2 deletion syndrome
    19. Primary pediatric care for children and youth with 22q11.2 deletion syndrome
    20. Healthcare transitions for adolescents and adults with 22q11.2 deletion syndrome
    21. Reproduction, prenatal screening, and diagnosis in 22q11.2 deletion syndrome
    22. Quality of life: Educational, vocational, and life planning for individuals with 22q11.2 deletion syndrome
    23. 22q11.2 deletion syndrome: Future directions
    24. General management principles for 22q11.2 deletion syndrome
    25. Medical needs associated with 22q11.2 deletion syndrome

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