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Angelman Syndrome

ISBN: 978-1-898683-55-1
256 pages
July 2008
Angelman Syndrome (1898683557) cover image

Description

Clinics in Developmental Medicine No. 177

This book provides a comprehensive review of clinical and genetic issues, natural history, possible pathophysiological pathways, specific clinical problems (motor impairment, behaviour, learning difficulties, communication, sleep, epilepsy), clinical neurophysiology, neuropathology, rehabilitation and basic research in the field of Angelman syndrome. This condition is a neurogenetic disorder characterised by developmental delay, absence of speech, motor impairment, epilepsy and a peculiar behavioural phenotype. It is caused by the lack of expression of the UBE3A gene associated with various abnormalities of chromosome 15q11-13.

Angelman syndrome appears to be distributed equally worldwide. Precise diagnosis carries clinical and genetic counselling implications. However, many clinicians still seem unfamiliar with this condition despite the severity and typical aspects of presentation. Beyond individual situations, Angelman syndrome can serve as a disease model opening broad questioning of genetic and epigenetic influences in neurology, as well as of several concepts such as psychomotor development, cerebral palsy, behavioural phenotypes and epileptic syndromes.

Recent advances in molecular biology and animal models of the syndrome have provided new data which can improve our understanding of Angelman syndrome and open the way to more specific management.

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Table of Contents

1. Doctor Angelman’s syndrome;.

2. Natural history.

3. A personal account.

4. Medical genetics;.

5. Molecular biology;.

6. Differential diagnosis;.

7. Behaviour;.

8. Perception and cognition;.

9. Communication;.

10. Movement and postural control;.

11. Epilepsy;.

12. Sleep;.

13. Clinical neurophysiology;.

14. Neuroimaging and neuropathology;.

15. Animal models;.

16. Perspectives;.

17. Resources. References

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The Wiley Advantage

● A comprehensive review of clinical and genetic issues, natural history, possible pathophysiological pathways, specific clinical problems, clinical neurophysiology, neuropathology, rehabilitation and basic research in the field of Angelman syndrome
● A neurogenetic disorder characterised by developmental delay, absence of speech, motor impairment, epilepsy and a distinctive behavioural phenotype
● Angelman syndrome is caused by the lack of expression of the UBE3A gene associated with various abnormalities of chromosome 15q11-13
● Features a wide range of photographic and graphic illustrations
● Includes chapter cross-referencing to ensure easy direction to development of topical issues
● Concludes each chapter with a critical summary featuring rehabilitation and research agenda
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-and- Fetal Behaviour: A Neurodevelopmental Approach (US $109.95)

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