Neurobiology, Diagnosis and Treatment in Autism - An Update
240 Pages
English

Neurobiology, Diagnosis and Treatment in Autism - An Update

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Description


This book provides an update on the progress made in the diagnosis, neurobiology and pharmacological treatment of autism and the rehabilitation of sufferers.  It looks set to have an influence on professional practices and thus modernise the approach to diagnosis and treatment.



Autism is a disease caused by an extremely complex neurological development abnormality which is expressed in a spectrum of phenotypes and is characterised by changes in normal social interactions and a restricted, stereotypical and repetitive range of interests and activities. Its etiopathogenesis remains poorly understood.



It has become evident that the genes responsible interact with environmental factors but the molecular and pathogenic factors resulting in expression of these mutations are still not clear. These genes involve several regions of the brain and not only cause neurotransmitter dysfunction but also affect other processes. These themes are explored in the first part of the book. The other chapters cover early intervention, discussing the most appropriate original rehabilitation methods and the results obtained with identical or similar protocols in Italian centres. Lastly, psychopharmacological options and the very common comorbidities are discussed.

Subjects

Informations

Published by
Published 02 September 2013
Reads 4
EAN13 9782742011858
License: All rights reserved
Language English

Legal information: rental price per page €. This information is given for information only in accordance with current legislation.

This book provides an update on the progress made in the diagnosis, neurobiology and pharmacological treatment of autism and the rehabilitation of sufferers.  It looks set to have an influence on professional practices and thus modernise the approach to diagnosis and treatment.
Autism is a disease caused by an extremely complex neurological development abnormality which is expressed in a spectrum of phenotypes and is characterised by changes in normal social interactions and a restricted, stereotypical and repetitive range of interests and activities. Its etiopathogenesis remains poorly understood.
It has become evident that the genes responsible interact with environmental factors but the molecular and pathogenic factors resulting in expression of these mutations are still not clear. These genes involve several regions of the brain and not only cause neurotransmitter dysfunction but also affect other processes. These themes are explored in the first part of the book. The other chapters cover early intervention, discussing the most appropriate original rehabilitation methods and the results obtained with identical or similar protocols in Italian centres. Lastly, psychopharmacological options and the very common comorbidities are discussed.
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