Based on a unique cohort study, this book identifies the complex care needs of people with Prader-Willi syndrome.Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Introduction Part I. Background: PWS, Why, What, and How To Investigate: 1. Background and historical overview 2. Biological and regulatory mechanisms in PWS 3. The Cambridge PWS project Part II. PWS Prevalence, Phenotypic Functioning and Characteristics: 4. Prevalence, birth incidence and mortality 5. Relationship between genetic and clinical diagnosis 6. Phenotypic differences between the genetic subtypes 7. Cognitive function and attainments 8. The behavioural phenotype of PWS 9. Medical conditions affecting people with PWS 10. Psychiatric illness 11. Obsessions and compulsions Part III. Minor Findings, Some Conclusions and Future Directions: 12. Understanding PWS Index.
Introduction Part I. Background: PWS, Why, What, and How To Investigate: 1. Background and historical overview 2. Biological and regulatory mechanisms in PWS 3. The Cambridge PWS project Part II. PWS Prevalence, Phenotypic Functioning and Characteristics: 4. Prevalence, birth incidence and mortality 5. Relationship between genetic and clinical diagnosis 6. Phenotypic differences between the genetic subtypes 7. Cognitive function and attainments 8. The behavioural phenotype of PWS 9. Medical conditions affecting people with PWS 10. Psychiatric illness 11. Obsessions and compulsions Part III. Minor Findings, Some Conclusions and Future Directions: 12. Understanding PWS Index.
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