Loading…
Genetic studies in children with intellectual disability and autistic spectrum of disorders
Autism is one of the five disorders that falls under the umbrella of Pervasive Developmental Disorders (PDD) or Autism Spectrum Disorder (ASD), a category of neurological disorders characterized by "severe and pervasive impairment in several areas of development." ASD is characterized by v...
Saved in:
Published in: | Indian journal of human genetics 2009-09, Vol.15 (3), p.103-107 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c4435-9b4fd436060763b3ff4c798360742b79e08792904e5e6fed21c028a16a22ad533 |
---|---|
cites | |
container_end_page | 107 |
container_issue | 3 |
container_start_page | 103 |
container_title | Indian journal of human genetics |
container_volume | 15 |
creator | Balasubramanian, Bhanumathi V Bhatt, Chetna A Goyel, Neelam |
description | Autism is one of the five disorders that falls under the umbrella of Pervasive Developmental Disorders (PDD) or Autism Spectrum Disorder (ASD), a category of neurological disorders characterized by "severe and pervasive impairment in several areas of development." ASD is characterized by varying degrees of impairment in communication skills, social interaction and restricted, repetitive stereotyped patterns of behavior. The five disorders under PDD are autistic disorder, Asperger's disorder, childhood disintegrative disorder, Rett's disorder and PDD-not otherwise specified. ASD can often be reliably detected by the age of 3 years and, in some cases, as early as 18 months. The appearance of any warning signs of ASD is reason to have the child evaluated by a professional specializing in these disorders. |
doi_str_mv | 10.4103/0971-6866.60185 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2922625</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A221245614</galeid><sourcerecordid>A221245614</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4435-9b4fd436060763b3ff4c798360742b79e08792904e5e6fed21c028a16a22ad533</originalsourceid><addsrcrecordid>eNqFks9rFDEUx4Modq2evcngxdNs82vy4yKUYqtQ8KIgeAiZ5M1uykyyJjNK__tmu3VRKUgOgfc-38fLN1-EXhO85gSzM6wlaYUSYi0wUd0TtCJaq5YJ-u0pWh27J-hFKTcYU0a5fo5OKMFKScJX6PsVRJiDa8q8-AClCbFx2zD6DLH5FeZtLcwwjuDmxY6ND8X2YQzzbWOjb-wyh3Kv3lUgL1OThj2TsodcXqJngx0LvHq4T9HXyw9fLj6215-vPl2cX7eOc9a1uueD50xggaVgPRsG7qRWtSA57aUGrKSmGnPoQAzgKXGYKkuEpdT6jrFT9P4wd7f0E3gHcc52NLscJptvTbLB_N2JYWs26aehmlJBuzrg3cOAnH4sUGYzheLqq22EtBSjsOKdVET-l5RcECqpxJV8-w95k5Ycqw-GaC5EJXWF2gO0sSOYEIdU93Ob-iV1zRRhCLV8TimhvBOEV379CF-Phym4RwVnB4HLqZQMw9EVgs0-QWafEbPPiLlPUFW8-dPMI_87MuwOA6zAUw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>194667469</pqid></control><display><type>article</type><title>Genetic studies in children with intellectual disability and autistic spectrum of disorders</title><source>Publicly Available Content Database</source><source>Portico (Triggered Content) Open Access</source><source>PubMed Central</source><creator>Balasubramanian, Bhanumathi ; V Bhatt, Chetna ; A Goyel, Neelam</creator><creatorcontrib>Balasubramanian, Bhanumathi ; V Bhatt, Chetna ; A Goyel, Neelam</creatorcontrib><description>Autism is one of the five disorders that falls under the umbrella of Pervasive Developmental Disorders (PDD) or Autism Spectrum Disorder (ASD), a category of neurological disorders characterized by "severe and pervasive impairment in several areas of development." ASD is characterized by varying degrees of impairment in communication skills, social interaction and restricted, repetitive stereotyped patterns of behavior. The five disorders under PDD are autistic disorder, Asperger's disorder, childhood disintegrative disorder, Rett's disorder and PDD-not otherwise specified. ASD can often be reliably detected by the age of 3 years and, in some cases, as early as 18 months. The appearance of any warning signs of ASD is reason to have the child evaluated by a professional specializing in these disorders.</description><identifier>ISSN: 0971-6866</identifier><identifier>EISSN: 1998-362X</identifier><identifier>DOI: 10.4103/0971-6866.60185</identifier><identifier>PMID: 21088714</identifier><language>eng</language><publisher>India: Medknow Publications and Media Pvt. Ltd</publisher><subject>Autism ; Behavior ; Children & youth ; Disability ; Genes ; Genetic aspects ; Genetic counseling ; Genetic disorders ; Genetic susceptibility ; Neurological disorders ; Original ; Risk factors ; Social interaction ; Studies</subject><ispartof>Indian journal of human genetics, 2009-09, Vol.15 (3), p.103-107</ispartof><rights>COPYRIGHT 2009 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt. Ltd. 2009</rights><rights>Indian Journal of Human Genetics 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4435-9b4fd436060763b3ff4c798360742b79e08792904e5e6fed21c028a16a22ad533</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2922625/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/194667469?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21088714$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Balasubramanian, Bhanumathi</creatorcontrib><creatorcontrib>V Bhatt, Chetna</creatorcontrib><creatorcontrib>A Goyel, Neelam</creatorcontrib><title>Genetic studies in children with intellectual disability and autistic spectrum of disorders</title><title>Indian journal of human genetics</title><addtitle>Indian J Hum Genet</addtitle><description>Autism is one of the five disorders that falls under the umbrella of Pervasive Developmental Disorders (PDD) or Autism Spectrum Disorder (ASD), a category of neurological disorders characterized by "severe and pervasive impairment in several areas of development." ASD is characterized by varying degrees of impairment in communication skills, social interaction and restricted, repetitive stereotyped patterns of behavior. The five disorders under PDD are autistic disorder, Asperger's disorder, childhood disintegrative disorder, Rett's disorder and PDD-not otherwise specified. ASD can often be reliably detected by the age of 3 years and, in some cases, as early as 18 months. The appearance of any warning signs of ASD is reason to have the child evaluated by a professional specializing in these disorders.</description><subject>Autism</subject><subject>Behavior</subject><subject>Children & youth</subject><subject>Disability</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic counseling</subject><subject>Genetic disorders</subject><subject>Genetic susceptibility</subject><subject>Neurological disorders</subject><subject>Original</subject><subject>Risk factors</subject><subject>Social interaction</subject><subject>Studies</subject><issn>0971-6866</issn><issn>1998-362X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqFks9rFDEUx4Modq2evcngxdNs82vy4yKUYqtQ8KIgeAiZ5M1uykyyJjNK__tmu3VRKUgOgfc-38fLN1-EXhO85gSzM6wlaYUSYi0wUd0TtCJaq5YJ-u0pWh27J-hFKTcYU0a5fo5OKMFKScJX6PsVRJiDa8q8-AClCbFx2zD6DLH5FeZtLcwwjuDmxY6ND8X2YQzzbWOjb-wyh3Kv3lUgL1OThj2TsodcXqJngx0LvHq4T9HXyw9fLj6215-vPl2cX7eOc9a1uueD50xggaVgPRsG7qRWtSA57aUGrKSmGnPoQAzgKXGYKkuEpdT6jrFT9P4wd7f0E3gHcc52NLscJptvTbLB_N2JYWs26aehmlJBuzrg3cOAnH4sUGYzheLqq22EtBSjsOKdVET-l5RcECqpxJV8-w95k5Ycqw-GaC5EJXWF2gO0sSOYEIdU93Ob-iV1zRRhCLV8TimhvBOEV379CF-Phym4RwVnB4HLqZQMw9EVgs0-QWafEbPPiLlPUFW8-dPMI_87MuwOA6zAUw</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Balasubramanian, Bhanumathi</creator><creator>V Bhatt, Chetna</creator><creator>A Goyel, Neelam</creator><general>Medknow Publications and Media Pvt. Ltd</general><general>Medknow Publications & Media Pvt. Ltd</general><general>Medknow Publications</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PADUT</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090901</creationdate><title>Genetic studies in children with intellectual disability and autistic spectrum of disorders</title><author>Balasubramanian, Bhanumathi ; V Bhatt, Chetna ; A Goyel, Neelam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4435-9b4fd436060763b3ff4c798360742b79e08792904e5e6fed21c028a16a22ad533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Autism</topic><topic>Behavior</topic><topic>Children & youth</topic><topic>Disability</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic counseling</topic><topic>Genetic disorders</topic><topic>Genetic susceptibility</topic><topic>Neurological disorders</topic><topic>Original</topic><topic>Risk factors</topic><topic>Social interaction</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Balasubramanian, Bhanumathi</creatorcontrib><creatorcontrib>V Bhatt, Chetna</creatorcontrib><creatorcontrib>A Goyel, Neelam</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Research Library China</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Indian journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Balasubramanian, Bhanumathi</au><au>V Bhatt, Chetna</au><au>A Goyel, Neelam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic studies in children with intellectual disability and autistic spectrum of disorders</atitle><jtitle>Indian journal of human genetics</jtitle><addtitle>Indian J Hum Genet</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>15</volume><issue>3</issue><spage>103</spage><epage>107</epage><pages>103-107</pages><issn>0971-6866</issn><eissn>1998-362X</eissn><abstract>Autism is one of the five disorders that falls under the umbrella of Pervasive Developmental Disorders (PDD) or Autism Spectrum Disorder (ASD), a category of neurological disorders characterized by "severe and pervasive impairment in several areas of development." ASD is characterized by varying degrees of impairment in communication skills, social interaction and restricted, repetitive stereotyped patterns of behavior. The five disorders under PDD are autistic disorder, Asperger's disorder, childhood disintegrative disorder, Rett's disorder and PDD-not otherwise specified. ASD can often be reliably detected by the age of 3 years and, in some cases, as early as 18 months. The appearance of any warning signs of ASD is reason to have the child evaluated by a professional specializing in these disorders.</abstract><cop>India</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><pmid>21088714</pmid><doi>10.4103/0971-6866.60185</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0971-6866 |
ispartof | Indian journal of human genetics, 2009-09, Vol.15 (3), p.103-107 |
issn | 0971-6866 1998-362X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2922625 |
source | Publicly Available Content Database; Portico (Triggered Content) Open Access; PubMed Central |
subjects | Autism Behavior Children & youth Disability Genes Genetic aspects Genetic counseling Genetic disorders Genetic susceptibility Neurological disorders Original Risk factors Social interaction Studies |
title | Genetic studies in children with intellectual disability and autistic spectrum of disorders |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T12%3A26%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genetic%20studies%20in%20children%20with%20intellectual%20disability%20and%20autistic%20spectrum%20of%20disorders&rft.jtitle=Indian%20journal%20of%20human%20genetics&rft.au=Balasubramanian,%20Bhanumathi&rft.date=2009-09-01&rft.volume=15&rft.issue=3&rft.spage=103&rft.epage=107&rft.pages=103-107&rft.issn=0971-6866&rft.eissn=1998-362X&rft_id=info:doi/10.4103/0971-6866.60185&rft_dat=%3Cgale_pubme%3EA221245614%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4435-9b4fd436060763b3ff4c798360742b79e08792904e5e6fed21c028a16a22ad533%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=194667469&rft_id=info:pmid/21088714&rft_galeid=A221245614&rfr_iscdi=true |