Mental retardation and developmental delay genetic and epigenetic factors

Recent advances in neuroscience and genetics have greatly expanded our understanding of the brain and of the etiological factors involved in developmental delay and mental retardation. At the same time, the human genome project has yielded a wealth of information on DNA sequencing, regulation of gen...

Full description

Saved in:
Bibliographic Details
Main Author: Smith, Moyra (Author)
Other Authors: Arfin, Stuart M, Lott, Ira T
Format: Book
Language:English
Published: Oxford Oxford University Press 2006
Subjects:
Online Access:Click Here to View Status and Holdings.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000nam a2200000#i 4501
001 wils-343198
005 20213193444
008 210401s2006 ENK a #001 deng D
020 # # |a 9780195174328  |q hardback 
020 # # |a 0195174321  |q hardback 
040 # # |a DNLM  |d UiTM  |e rda 
041 0 # |a English 
060 0 0 |a WS 107.5.B4 
090 0 0 |a WS107.5.B4  |b S655m 2006 
100 1 # |a Smith, Moyra  |e author 
245 1 0 |a Mental retardation and developmental delay  |b genetic and epigenetic factors  |c Moyra Smith 
264 # 1 |a Oxford  |b Oxford University Press  |c 2006 
300 # # |a xix, 317 pages  |b illustrations  |c 25 cm 
336 # # |a text  |b txt  |2 rdacontent 
337 # # |a unmediated  |b n  |2 rdamedia 
338 # # |a volume  |b nc  |2 rdacarrier 
504 # # |a Includes bibliographical references (p. 247-300) and index 
520 # # |a Recent advances in neuroscience and genetics have greatly expanded our understanding of the brain and of the etiological factors involved in developmental delay and mental retardation. At the same time, the human genome project has yielded a wealth of information on DNA sequencing, regulation of gene expression, epigenetics, and functional aspects of the genome, which newly propels investigation into the pathogenesis of mental retardation. This book makes readily available current knowledge on the subject and applies it to clinical medicine, providing information essential to neurologists, geneticists, physicians and pediatricians as they search for the causes of mental handicap in their patients. Introductory chapters cover normal and abnormal brain structure, neurogenesis, neuronal proliferation, and signal transduction. Latter chapters delve into discussions of both the environmental factors that may lead to neurocognitive deficits and the cytogenetic, biochemical and molecular defects specifically associated with mental retardation. One chapter reviews gene involvement in non-syndromic mental retardation, autism, and language deficits, as well as multifactorial and genetically complex inheritance. The text concludes with a clinically practical discussion of carrier detection, presymptomatic diagnosis, and treatment of various genetic diseases through enzyme therapy, substrate deprivation, and the use of hemapoietic stem cells 
650 1 2 |a Child 
650 2 2 |a Developmental Disabilities  |x etiology 
650 2 2 |a Developmental Disabilities  |x genetics 
650 2 2 |a Infant 
650 2 2 |a Intellectual Disability  |x etiology 
700 1 # |a Arfin, Stuart M 
700 # # |a Lott, Ira T 
856 4 0 |z Click Here to View Status and Holdings.  |u https://opac.uitm.edu.my/opac/detailsPage/detailsHome.jsp?tid=343198 
964 # # |c BOK  |d 01 
998 # # |a 00264#1a002.8.2||00264#1b002.8.4||00300##a003.4.1||00300##b003.6.1||00300##c003.5.1||00520##a007.2||00520##b007.2||01700##a0011.2.2||