
Prader-Willi Syndrome
Development and Manifestations
- Publisher's listprice GBP 125.00
-
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.
- Discount 20% (cc. 12 652 Ft off)
- Discounted price 50 610 Ft (48 200 Ft + 5% VAT)
Subcribe now and take benefit of a favourable price.
Subscribe
63 262 Ft
Availability
Estimated delivery time: In stock at the publisher, but not at Prospero's office. Delivery time approx. 3-5 weeks.
Not in stock at Prospero.
Why don't you give exact delivery time?
Delivery time is estimated on our previous experiences. We give estimations only, because we order from outside Hungary, and the delivery time mainly depends on how quickly the publisher supplies the book. Faster or slower deliveries both happen, but we do our best to supply as quickly as possible.
Product details:
- Publisher Cambridge University Press
- Date of Publication 22 April 2004
- ISBN 9780521840293
- Binding Hardback
- No. of pages232 pages
- Size 255x180x19 mm
- Weight 766 g
- Language English 0
Categories
Short description:
Based on a unique cohort study, this book identifies the complex care needs of people with Prader-Willi syndrome.
MoreLong description:
Prader-Willi syndrome (PWS) is associated with an assortment of physical, behavioural and cognitive abnormalities which create a broad range of care needs. Information about the syndrome is spread across a variety of disciplines. In this book the authors seek to identify and provide the latest findings about how best to manage the complex medical, nutritional, psychological, educational, social and therapeutic needs of people with PWS. Their approach is an integrated one, centred on the PWS phenotype. Both authors have been involved in the Cambridge PWS study, which is the largest and most rounded of the cohort studies of PWS anywhere in the world. The unique data it provides is the basis of this book.
Review of the hardback: 'It is a representative compilation of the knowledge of today ... can be recommended to all readers interested in genetics and their connections to different human functions. Even parents of children with PWS who want to know where the front line of research is will find this book valuable.' European Child & Adolescent Psychiatry
Table of Contents:
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.
More