Preventive Health Care for Children with Genetic Conditions: Providing a Primary Care Medical Home

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Edition: 2nd
Format: Paperback
Pub. Date: 2006-05-29
Publisher(s): Cambridge University Press
List Price: $153.00

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Summary

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.

Author Biography

Golder Wilson as clinical Professor of Pediatrics at Texas Tech university W. Carl Cooley is Adjunct Associate Professor of Pediatrics at Dartmouth Medical School and the Director of the Crotched Mountain Rehabilitation Center in New Hampshire

Table of Contents

Preface ix
Glossary of genetic and molecular terms xv
Part I Approach to the child with special needs
Approach to the child with genetic disease
3(18)
Providing a primary care medical home for the child with a developmental disability
21(12)
Approach to preventive management
33(28)
Part II The management of selected single congenital anomalies and associations
Congenital anomalies associated with developmental disability
61(29)
Single anomalies, sequences, and associations
90(26)
Teratogenic syndromes
116(35)
Part III Chromosomal syndromes
Autosomal aneuploidy syndromes
151(43)
Sex chromosome aneuploidy and X-linked mental retardation syndromes
194(36)
Chromosome microdeletion syndromes
230(35)
Part IV Syndromes remarkable for altered growth
Syndromes with proportionate growth failure as a primary manifestation
265(28)
Syndromes with disproportionate growth failure (dwarfism)
293(33)
Overgrowth syndromes
326(20)
Hamartosis syndromes
346(29)
Part V Management of craniofacial syndromes
Craniosynostosis syndromes
375(13)
Branchial arch and face/limb syndromes
388(25)
Part VI Management of connective tissue and integumentary syndromes
Connective tissue disorders
413(24)
Integumentary syndromes
437(20)
Part VII The management of neurologic and neurodegenerative syndromes
Neurologic syndromes including the arthrogryposes
457(20)
Part VIII Management of neurodegenerative metabolic disorders
Organellar and miscellaneous neurodegenerative disorders
477(29)
Metabolic dysplasias susceptible to dietary treatment
506(18)
References 524(25)
Index 549

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