Nicht aus der Schweiz? Besuchen Sie lehmanns.de
Preventive Health Care for Children with Genetic Conditions - Golder N. Wilson, W. Carl Cooley

Preventive Health Care for Children with Genetic Conditions

Providing a Primary Care Medical Home
Buch | Softcover
582 Seiten
2006 | 2nd Revised edition
Cambridge University Press (Verlag)
978-0-521-61734-5 (ISBN)
CHF 214,70 inkl. MwSt
This updated new edition provides health professionals with an invaluable, structured approach to the preventive care of children with congenital disorders. Over 150 conditions ranging from cerebral palsy to Down syndrome are discussed.
Originally published as Preventative Management of Children with Congenital Anomalies and Syndromes, this new edition provides health professionals with an invaluable, structured approach to the preventive care of children with congenital disorders. Over 150 conditions ranging from cerebral palsy to Down syndrome are discussed. The large number of conditions covered and the added perspective of a developmental pediatrician (Dr Cooley) provides a valuable resource for carers and parents. For each disorder there is an introductory summary of key information, followed by more detailed listing of general pediatric and speciality concerns, all structured to provide an integrated approach to patient care. For 32 common disorders or disease categories, preventive management checklists are provided: these checklists provide an ongoing record for the child's medical complications and progress and they are designed to be copied and placed in the medical record. The text provides details of medical complications and preventive recommendations supported by key literature and web resources for parents and professionals.

Preface; Part I. Approach to the Child with Special Needs: 1. Approach to the child with genetic disease; 2. Providing a primary care medical home for the child with developmental disability; 3. Approach to preventive management; Part II. The Management of Selected Single Congenital Anomalies and Associations: 4. Congenital anomalies associated with developmental disability; 5. Single anomalies, sequences and associations; 6. Teratogenic syndromes; Part III. Chromosomal Syndromes: 7. Autosomal aneuploidy syndromes; 8. Sex chromosome aneuploidy and X-linked mental retardation; 9. Chromosome microdeletion syndromes; Part IV. Syndromes Remarkable for Altered Growth: 10. Syndromes with proportionate growth failure as a primary manifestation; 11. Syndromes with disproportionate growth failure; 12. Overgrowth syndromes; 13. Hamartosis syndrome; Part V. Management of Craniofacial Syndromes: 14. Craniosynostosis syndromes; 15. Branchial arch and face/limb syndrome; Part VI. Management of Connective Tissue and Integumentary Syndromes: 16. Connective tissue disorders; 17. Integumentary syndromes; Part VII. Management of Neurologic and Neurodegenerative Syndromes: 18. Neurologic syndromes including the arthrogryposes; Part VIII. Management of Neurodegenerative Metabolic Disorders; 19. Organellar and miscellaneous neurodegenerative disorders; 20. Metabolic dysplasias susceptible to dietary treatment; References; Index.

Erscheint lt. Verlag 11.5.2006
Zusatzinfo 30 Tables, unspecified; 3 Line drawings, unspecified
Verlagsort Cambridge
Sprache englisch
Maße 174 x 247 mm
Gewicht 1160 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pädiatrie
ISBN-10 0-521-61734-0 / 0521617340
ISBN-13 978-0-521-61734-5 / 9780521617345
Zustand Neuware
Haben Sie eine Frage zum Produkt?
Mehr entdecken
aus dem Bereich
Inklusive Neonatologie/ Intensivmedizin

von Dietmar Wigger; Markus Stange

Buch | Softcover (2020)
Urban & Fischer in Elsevier (Verlag)
CHF 38,00
Grundlagen, Klinik und Praxis

von Ertan Mayatepek

Buch | Hardcover (2023)
Urban & Fischer in Elsevier (Verlag)
CHF 179,95