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1048 lines
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<!--
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||
UID=453059
|
||
ConceptID=C1535926
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Neurodevelopmental disorder</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>453059</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1535926</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Child Mental Disorder; Child Mental Disorders; Disorder, Child Mental; Disorder, Neurodevelopmental; Mental Disorder, Child; Mental Disorders Diagnosed in Childhood; Mental Disorders Usually Diagnosed in Infancy, Childhood or Adolescence; Mental Disorders, Child; Neurodevelopmental Disorder; Neurodevelopmental Disorders; Neurodevelopmental Disorders Usually Diagnosed in Infancy, Childhood or Adolescence</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Neurodevelopmental disorder (700364009)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0700092" target="_blank">MONDO:0700092</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln">Neurodevelopmental disorder is a behavioral and cognitive disorder with onset during the developmental period that involves impaired or aberrant development of intellectual, motor, or social functions. [from <a title="US Edition of SNOMED CT" href="http://www.nlm.nih.gov/research/umls/Snomed/us_edition.html" class="defSource" target="_blank">SNOMEDCT_US</a>]</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1535926[DISCUI]&test_type=Clinical&redirect=true" ref="ncbi_uid=453059">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=453059" ref="ncbi_uid=453059">V</a></span></span><span class="TLline">Neurodevelopmental disorder</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="matched_ds">Neurodevelopmental disorder</span><ul><li><span class="TLline"><a href="/medgen/3367" ref="tree=MeSH" title="MedGen record for Developmental disorder">Developmental disorder</a></span><ul><li><span class="matched_ds">Neurodevelopmental disorder</span><ul><li><span class="TLline"><a href="/medgen/3367" ref="tree=MeSH" title="MedGen record for Developmental disorder">Developmental disorder</a></span><ul><li><span class="matched_ds">Neurodevelopmental disorder</span><ul><li><span class="TLline"><a href="/medgen/3367" ref="tree=MeSH" title="MedGen record for Developmental disorder">Developmental disorder</a></span><ul><li><span class="matched_ds">Neurodevelopmental disorder</span><ul><li><span class="TLline"><a href="/medgen/68635" ref="tree=MeSH" title="MedGen record for Attention Deficit and Disruptive Behavior Disorders">Attention Deficit and Disruptive Behavior Disorders</a></span><ul><li><span class="TLline"><a href="/medgen/220387" ref="tree=MeSH" title="MedGen record for Attention deficit hyperactivity disorder">Attention deficit hyperactivity disorder</a></span><ul><li><span class="TLline"><a href="/medgen/473060" ref="tree=MeSH" title="MedGen record for Attention deficit hyperactivity disorder, inattentive type">Attention deficit hyperactivity disorder, inattentive type</a></span></li><li><span class="TLline"><a href="/medgen/1004009" ref="tree=MeSH" title="MedGen record for Hereditary attention deficit-hyperactivity disorder">Hereditary attention deficit-hyperactivity disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/56196" ref="tree=MeSH" title="MedGen record for conduct disorder">conduct disorder</a></span></li><li><span class="TLline"><a href="/medgen/1789130" ref="tree=MeSH" title="MedGen record for Sluggish Cognitive Tempo">Sluggish Cognitive Tempo</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/474392" ref="tree=MeSH" title="MedGen record for Brain Development Abnormality">Brain Development Abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/324748" ref="tree=MeSH" title="MedGen record for Abnormality of neuronal migration">Abnormality of neuronal migration</a></span><ul><li><span class="TLline"><a href="/medgen/408200" ref="tree=MeSH" title="MedGen record for Classical Lissencephalies and Subcortical Band Heterotopias">Classical Lissencephalies and Subcortical Band Heterotopias</a></span></li><li><span class="TLline"><a href="/medgen/96562" ref="tree=MeSH" title="MedGen record for Cobblestone lissencephaly">Cobblestone lissencephaly</a></span></li><li><span class="TLline"><a href="/medgen/452349" ref="tree=MeSH" title="MedGen record for Gray matter heterotopia">Gray matter heterotopia</a></span></li><li><span class="TLline"><a href="/medgen/78604" ref="tree=MeSH" title="MedGen record for Lissencephaly">Lissencephaly</a></span></li><li><span class="TLline"><a href="/medgen/358387" ref="tree=MeSH" title="MedGen record for Periventricular nodular heterotopia">Periventricular nodular heterotopia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/6937" ref="tree=MeSH" title="MedGen record for Hydranencephaly">Hydranencephaly</a></span></li><li><span class="TLline"><a href="/medgen/44422" ref="tree=MeSH" title="MedGen record for Isolated congenital microcephaly">Isolated congenital microcephaly</a></span><ul><li><span class="TLline"><a href="/medgen/66319" ref="tree=MeSH" title="MedGen record for Autosomal dominant primary microcephaly">Autosomal dominant primary microcephaly</a></span></li><li><span class="TLline"><a href="/medgen/777995" ref="tree=MeSH" title="MedGen record for Autosomal recessive primary microcephaly">Autosomal recessive primary microcephaly</a></span></li><li><span class="TLline"><a href="/medgen/901502" ref="tree=MeSH" title="MedGen record for Porencephaly">Porencephaly</a></span></li><li><span class="TLline"><a href="/medgen/383046" ref="tree=MeSH" title="MedGen record for Primary microcephaly">Primary microcephaly</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/386642" ref="tree=MeSH" title="MedGen record for microgyria">microgyria</a></span></li><li><span class="TLline"><a href="/medgen/420956" ref="tree=MeSH" title="MedGen record for Pontocerebellar hypoplasia type 2">Pontocerebellar hypoplasia type 2</a></span><ul><li><span class="TLline"><a href="/medgen/376379" ref="tree=MeSH" title="MedGen record for Pontocerebellar hypoplasia type 2A">Pontocerebellar hypoplasia type 2A</a></span></li><li><span class="TLline"><a href="/medgen/393505" ref="tree=MeSH" title="MedGen record for Pontocerebellar hypoplasia type 2B">Pontocerebellar hypoplasia type 2B</a></span></li><li><span class="TLline"><a href="/medgen/382856" ref="tree=MeSH" title="MedGen record for Pontocerebellar hypoplasia type 2C">Pontocerebellar hypoplasia type 2C</a></span></li><li><span class="TLline"><a href="/medgen/462490" ref="tree=MeSH" title="MedGen record for Pontocerebellar hypoplasia type 2D">Pontocerebellar hypoplasia type 2D</a></span></li><li><span class="TLline"><a href="/medgen/862925" ref="tree=MeSH" title="MedGen record for Pontocerebellar hypoplasia type 2E">Pontocerebellar hypoplasia type 2E</a></span></li><li><span class="TLline"><a href="/medgen/934724" ref="tree=MeSH" title="MedGen record for Pontocerebellar hypoplasia, type 2F">Pontocerebellar hypoplasia, type 2F</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/336288" ref="tree=MeSH" title="MedGen record for Subcortical band heterotopia">Subcortical band heterotopia</a></span><ul><li><span class="TLline"><a href="/medgen/1703799" ref="tree=MeSH" title="MedGen record for Anterior predominant subcortical band heterotopia">Anterior predominant subcortical band heterotopia</a></span></li><li><span class="TLline"><a href="/medgen/1689721" ref="tree=MeSH" title="MedGen record for Diffuse subcortical band heterotopia">Diffuse subcortical band heterotopia</a></span></li><li><span class="TLline"><a href="/medgen/1691332" ref="tree=MeSH" title="MedGen record for Posterior predominant subcortical band heterotopia">Posterior predominant subcortical band heterotopia</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/2998" ref="tree=MeSH" title="MedGen record for Child Behavior Disorders">Child Behavior Disorders</a></span></li><li><span class="TLline"><a href="/medgen/887" ref="tree=MeSH" title="MedGen record for Child Development Disorders, Pervasive">Child Development Disorders, Pervasive</a></span><ul><li><span class="TLline"><a href="/medgen/307153" ref="tree=MeSH" title="MedGen record for Autism spectrum disorder">Autism spectrum disorder</a></span><ul><li><span class="TLline"><a href="/medgen/68633" ref="tree=MeSH" title="MedGen record for Asperger syndrome">Asperger syndrome</a></span></li><li><span class="TLline"><a href="/medgen/13966" ref="tree=MeSH" title="MedGen record for Autism">Autism</a></span></li><li><span class="TLline"><a href="/medgen/369890" ref="tree=MeSH" title="MedGen record for Autism, susceptibility to, 1">Autism, susceptibility to, 1</a></span></li><li><span class="TLline"><a href="/medgen/334211" ref="tree=MeSH" title="MedGen record for Autism, susceptibility to, 3">Autism, susceptibility to, 3</a></span></li><li><span class="TLline"><a href="/medgen/340048" ref="tree=MeSH" title="MedGen record for Autism, susceptibility to, 5">Autism, susceptibility to, 5</a></span></li><li><span class="TLline"><a href="/medgen/324472" ref="tree=MeSH" title="MedGen record for Autism, susceptibility to, 6">Autism, susceptibility to, 6</a></span></li><li><span class="TLline"><a href="/medgen/410155" ref="tree=MeSH" title="MedGen record for Autism, susceptibility to, 7">Autism, susceptibility to, 7</a></span></li><li><span class="TLline"><a href="/medgen/409897" ref="tree=MeSH" title="MedGen record for Autism, susceptibility to, 8">Autism, susceptibility to, 8</a></span></li><li><span class="TLline"><a href="/medgen/336964" ref="tree=MeSH" title="MedGen record for Autism, susceptibility to, X-linked 2">Autism, susceptibility to, X-linked 2</a></span></li><li><span class="TLline"><a href="/medgen/335161" ref="tree=MeSH" title="MedGen record for Autism, susceptibility to, X-linked 3">Autism, susceptibility to, X-linked 3</a></span></li><li><span class="TLline"><a href="/medgen/985929" ref="tree=MeSH" title="MedGen record for Autism, susceptiblity to">Autism, susceptiblity to</a></span></li><li><span class="TLline"><a href="/medgen/472967" ref="tree=MeSH" title="MedGen record for Childhood disintegrative disorder">Childhood disintegrative disorder</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/48576" ref="tree=MeSH" title="MedGen record for Childhood-onset schizophrenia">Childhood-onset schizophrenia</a></span></li><li><span class="TLline"><a href="/medgen/3549" ref="tree=MeSH" title="MedGen record for communication disorder">communication disorder</a></span><ul><li><span class="TLline"><a href="/medgen/754254" ref="tree=MeSH" title="MedGen record for Childhood onset fluency disorder">Childhood onset fluency disorder</a></span></li><li><span class="TLline"><a href="/medgen/57707" ref="tree=MeSH" title="MedGen record for Impaired social interactions">Impaired social interactions</a></span></li><li><span class="TLline"><a href="/medgen/44069" ref="tree=MeSH" title="MedGen record for Language disorder">Language disorder</a></span><ul><li><span class="TLline"><a href="/medgen/1790" ref="tree=MeSH" title="MedGen record for Agraphia">Agraphia</a></span></li><li><span class="TLline"><a href="/medgen/312" ref="tree=MeSH" title="MedGen record for Anomic aphasia">Anomic aphasia</a></span></li><li><span class="TLline"><a href="/medgen/870509" ref="tree=MeSH" title="MedGen record for Deficit in grammar">Deficit in grammar</a></span></li><li><span class="TLline"><a href="/medgen/6010" ref="tree=MeSH" title="MedGen record for Developmental language disorder">Developmental language disorder</a></span></li><li><span class="TLline"><a href="/medgen/96906" ref="tree=MeSH" title="MedGen record for Dyslexia">Dyslexia</a></span></li><li><span class="TLline"><a href="/medgen/452300" ref="tree=MeSH" title="MedGen record for expressive language disorder">expressive language disorder</a></span></li><li><span class="TLline"><a href="/medgen/452301" ref="tree=MeSH" title="MedGen record for mixed receptive-expressive language disorder">mixed receptive-expressive language disorder</a></span></li><li><span class="TLline"><a href="/medgen/881467" ref="tree=MeSH" title="MedGen record for Phonological disorder">Phonological disorder</a></span></li><li><span class="TLline"><a href="/medgen/400736" ref="tree=MeSH" title="MedGen record for Speech articulation difficulties">Speech articulation difficulties</a></span></li><li><span class="TLline"><a href="/medgen/11531" ref="tree=MeSH" title="MedGen record for Speech disorder">Speech disorder</a></span></li><li><span class="TLline"><a href="/medgen/892986" ref="tree=MeSH" title="MedGen record for Spoken word recognition deficit">Spoken word recognition deficit</a></span></li><li><span class="TLline"><a href="/medgen/20981" ref="tree=MeSH" title="MedGen record for Stuttering">Stuttering</a></span></li><li><span class="TLline"><a href="/medgen/535439" ref="tree=MeSH" title="MedGen record for Word salad">Word salad</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/199623" ref="tree=MeSH" title="MedGen record for Learning disability">Learning disability</a></span><ul><li><span class="TLline"><a href="/medgen/1790513" ref="tree=MeSH" title="MedGen record for Acalculia">Acalculia</a></span></li><li><span class="TLline"><a href="/medgen/875797" ref="tree=MeSH" title="MedGen record for Learning Disorder, Specific">Learning Disorder, Specific</a></span></li><li><span class="TLline"><a href="/medgen/627772" ref="tree=MeSH" title="MedGen record for Specific language impairment">Specific language impairment</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/866372" ref="tree=MeSH" title="MedGen record for Speech-sound disorder">Speech-sound disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/488957" ref="tree=MeSH" title="MedGen record for Congenital meningocele">Congenital meningocele</a></span><ul><li><span class="TLline"><a href="/medgen/507591" ref="tree=MeSH" title="MedGen record for Congenital cerebral meningocele">Congenital cerebral meningocele</a></span></li><li><span class="TLline"><a href="/medgen/507597" ref="tree=MeSH" title="MedGen record for Congenital spinal meningocele">Congenital spinal meningocele</a></span><ul><li><span class="TLline"><a href="/medgen/768674" ref="tree=MeSH" title="MedGen record for Cervical Meningocele">Cervical Meningocele</a></span></li><li><span class="TLline"><a href="/medgen/768675" ref="tree=MeSH" title="MedGen record for Lumbar Meningocele">Lumbar Meningocele</a></span></li><li><span class="TLline"><a href="/medgen/101069" ref="tree=MeSH" title="MedGen record for Sacral meningocele">Sacral meningocele</a></span></li><li><span class="TLline"><a href="/medgen/768676" ref="tree=MeSH" title="MedGen record for Thoracic Meningocele">Thoracic Meningocele</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/3367" ref="tree=MeSH" title="MedGen record for Developmental disorder">Developmental disorder</a></span><ul><li><span class="TLline"><a href="/medgen/41511" ref="tree=MeSH" title="MedGen record for Developmental coordination disorder">Developmental coordination disorder</a></span></li><li><span class="TLline"><a href="/medgen/98410" ref="tree=MeSH" title="MedGen record for Developmental delay">Developmental delay</a></span><ul><li><span class="TLline"><a href="/medgen/381392" ref="tree=MeSH" title="MedGen record for Motor delay">Motor delay</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/324613" ref="tree=MeSH" title="MedGen record for Developmental regression">Developmental regression</a></span><ul><li><span class="TLline"><a href="/medgen/815091" ref="tree=MeSH" title="MedGen record for Cognitive regression">Cognitive regression</a></span></li><li><span class="TLline"><a href="/medgen/478627" ref="tree=MeSH" title="MedGen record for Motor regression">Motor regression</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/7544" ref="tree=MeSH" title="MedGen record for Mental Retardation">Mental Retardation</a></span><ul><li><span class="TLline"><a href="/medgen/862975" ref="tree=MeSH" title="MedGen record for ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder">ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder</a></span></li><li><span class="TLline"><a href="/medgen/337145" ref="tree=MeSH" title="MedGen record for Alpha thalassemia-X-linked intellectual disability syndrome">Alpha thalassemia-X-linked intellectual disability syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78557" ref="tree=MeSH" title="MedGen record for Borjeson-Forssman-Lehmann syndrome">Borjeson-Forssman-Lehmann syndrome</a></span></li><li><span class="TLline"><a href="/medgen/394455" ref="tree=MeSH" title="MedGen record for Christianson syndrome">Christianson syndrome</a></span></li><li><span class="TLline"><a href="/medgen/409857" ref="tree=MeSH" title="MedGen record for Intellectual disability, autosomal dominant 1">Intellectual disability, autosomal dominant 1</a></span></li><li><span class="TLline"><a href="/medgen/382611" ref="tree=MeSH" title="MedGen record for Intellectual disability, autosomal dominant 5">Intellectual disability, autosomal dominant 5</a></span></li><li><span class="TLline"><a href="/medgen/909304" ref="tree=MeSH" title="MedGen record for Intellectual disability, autosomal dominant 39">Intellectual disability, autosomal dominant 39</a></span></li><li><span class="TLline"><a href="/medgen/482674" ref="tree=MeSH" title="MedGen record for Intellectual disability, autosomal recessive 34">Intellectual disability, autosomal recessive 34</a></span></li><li><span class="TLline"><a href="/medgen/444070" ref="tree=MeSH" title="MedGen record for Intellectual disability, X-linked 1">Intellectual disability, X-linked 1</a></span></li><li><span class="TLline"><a href="/medgen/894460" ref="tree=MeSH" title="MedGen record for Mental Retardation, Autosomal Dominant 40">Mental Retardation, Autosomal Dominant 40</a></span></li><li><span class="TLline"><a href="/medgen/897961" ref="tree=MeSH" title="MedGen record for Mental Retardation, X-linked 102">Mental Retardation, X-linked 102</a></span></li><li><span class="TLline"><a href="/medgen/1790595" ref="tree=MeSH" title="MedGen record for Mental Retardation, X-linked 21/34">Mental Retardation, X-linked 21/34</a></span></li><li><span class="TLline"><a href="/medgen/208670" ref="tree=MeSH" title="MedGen record for Renpenning syndrome">Renpenning syndrome</a></span></li><li><span class="TLline"><a href="/medgen/767363" ref="tree=MeSH" title="MedGen record for Severe intellectual disability-progressive spastic diplegia syndrome">Severe intellectual disability-progressive spastic diplegia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/337496" ref="tree=MeSH" title="MedGen record for Syndromic X-linked intellectual disability Lubs type">Syndromic X-linked intellectual disability Lubs type</a></span></li><li><span class="TLline"><a href="/medgen/337334" ref="tree=MeSH" title="MedGen record for X-linked intellectual disability Cabezas type">X-linked intellectual disability Cabezas type</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1769271" ref="tree=MeSH" title="MedGen record for Naevus Lipomatosus Superficialis">Naevus Lipomatosus Superficialis</a></span></li><li><span class="TLline"><a href="/medgen/508088" ref="tree=MeSH" title="MedGen record for Reactive Attachment Disorder of Infancy or Early Childhood">Reactive Attachment Disorder of Infancy or Early Childhood</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/769787" ref="tree=MeSH" title="MedGen record for Fetal Neurodevelopmental Disorder">Fetal Neurodevelopmental Disorder</a></span></li><li><span class="TLline"><a href="/medgen/1375401" ref="tree=MeSH" title="MedGen record for Gabriele de Vries syndrome">Gabriele de Vries syndrome</a></span></li><li><span class="TLline"><a href="/medgen/811461" ref="tree=MeSH" title="MedGen record for Intellectual disability">Intellectual disability</a></span><ul><li><span class="TLline"><a href="/medgen/64512" ref="tree=MeSH" title="MedGen record for 11p partial monosomy syndrome">11p partial monosomy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/41345" ref="tree=MeSH" title="MedGen record for 5p partial monosomy syndrome">5p partial monosomy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/78752" ref="tree=MeSH" title="MedGen record for De Lange syndrome">De Lange syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/315658" ref="tree=MeSH" title="MedGen record for Congenital muscular hypertrophy-cerebral syndrome">Congenital muscular hypertrophy-cerebral syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1645760" ref="tree=MeSH" title="MedGen record for Cornelia de Lange syndrome 1">Cornelia de Lange syndrome 1</a></span></li><li><span class="TLline"><a href="/medgen/339902" ref="tree=MeSH" title="MedGen record for Cornelia de Lange syndrome 3">Cornelia de Lange syndrome 3</a></span></li><li><span class="TLline"><a href="/medgen/766431" ref="tree=MeSH" title="MedGen record for Cornelia de Lange syndrome 4">Cornelia de Lange syndrome 4</a></span></li><li><span class="TLline"><a href="/medgen/763817" ref="tree=MeSH" title="MedGen record for Cornelia de Lange syndrome 5">Cornelia de Lange syndrome 5</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/4385" ref="tree=MeSH" title="MedGen record for Down syndrome">Down syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/693553" ref="tree=MeSH" title="MedGen record for Translocation Down syndrome">Translocation Down syndrome</a></span></li><li><span class="TLline"><a href="/medgen/760825" ref="tree=MeSH" title="MedGen record for Trisomy 21">Trisomy 21</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/507499" ref="tree=MeSH" title="MedGen record for Intellectual disability, borderline">Intellectual disability, borderline</a></span></li><li><span class="TLline"><a href="/medgen/10044" ref="tree=MeSH" title="MedGen record for Intellectual disability, mild">Intellectual disability, mild</a></span></li><li><span class="TLline"><a href="/medgen/7680" ref="tree=MeSH" title="MedGen record for Intellectual disability, moderate">Intellectual disability, moderate</a></span></li><li><span class="TLline"><a href="/medgen/892508" ref="tree=MeSH" title="MedGen record for Intellectual disability, profound">Intellectual disability, profound</a></span></li><li><span class="TLline"><a href="/medgen/337397" ref="tree=MeSH" title="MedGen record for Intellectual disability, progressive">Intellectual disability, progressive</a></span></li><li><span class="TLline"><a href="/medgen/48638" ref="tree=MeSH" title="MedGen record for Intellectual disability, severe">Intellectual disability, severe</a></span></li><li><span class="TLline"><a href="/medgen/46057" ref="tree=MeSH" title="MedGen record for Prader-Willi syndrome">Prader-Willi syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/1826086" ref="tree=MeSH" title="MedGen record for Prader-Willi syndrome due to imprinting mutation">Prader-Willi syndrome due to imprinting mutation</a></span></li><li><span class="TLline"><a href="/medgen/1826079" ref="tree=MeSH" title="MedGen record for Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15">Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15</a></span></li><li><span class="TLline"><a href="/medgen/1826129" ref="tree=MeSH" title="MedGen record for Prader-Willi syndrome due to paternal 15q11q13 deletion">Prader-Willi syndrome due to paternal 15q11q13 deletion</a></span></li><li><span class="TLline"><a href="/medgen/1826085" ref="tree=MeSH" title="MedGen record for Prader-Willi syndrome due to translocation">Prader-Willi syndrome due to translocation</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/48517" ref="tree=MeSH" title="MedGen record for Rubinstein-Taybi syndrome">Rubinstein-Taybi syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/350477" ref="tree=MeSH" title="MedGen record for Rubinstein-Taybi syndrome due to 16p13.3 microdeletion">Rubinstein-Taybi syndrome due to 16p13.3 microdeletion</a></span></li><li><span class="TLline"><a href="/medgen/1639327" ref="tree=MeSH" title="MedGen record for Rubinstein-Taybi syndrome due to CREBBP mutations">Rubinstein-Taybi syndrome due to CREBBP mutations</a></span></li><li><span class="TLline"><a href="/medgen/462291" ref="tree=MeSH" title="MedGen record for Rubinstein-Taybi syndrome due to EP300 haploinsufficiency">Rubinstein-Taybi syndrome due to EP300 haploinsufficiency</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1379406" ref="tree=MeSH" title="MedGen record for Trisomy 13 Syndromes">Trisomy 13 Syndromes</a></span></li><li><span class="TLline"><a href="/medgen/59799" ref="tree=MeSH" title="MedGen record for Williams syndrome">Williams syndrome</a></span></li><li><span class="TLline"><a href="/medgen/211749" ref="tree=MeSH" title="MedGen record for X-linked intellectual disability">X-linked intellectual disability</a></span><ul><li><span class="TLline"><a href="/medgen/57667" ref="tree=MeSH" title="MedGen record for Adrenoleukodystrophy">Adrenoleukodystrophy</a></span></li><li><span class="TLline"><a href="/medgen/75556" ref="tree=MeSH" title="MedGen record for Coffin-Lowry syndrome">Coffin-Lowry syndrome</a></span></li><li><span class="TLline"><a href="/medgen/209235" ref="tree=MeSH" title="MedGen record for Danon disease">Danon disease</a></span></li><li><span class="TLline"><a href="/medgen/8912" ref="tree=MeSH" title="MedGen record for Fragile X syndrome">Fragile X syndrome</a></span></li><li><span class="TLline"><a href="/medgen/9721" ref="tree=MeSH" title="MedGen record for Lesch-Nyhan syndrome">Lesch-Nyhan syndrome</a></span></li><li><span class="TLline"><a href="/medgen/44030" ref="tree=MeSH" title="MedGen record for Menkes kinky-hair syndrome">Menkes kinky-hair syndrome</a></span></li><li><span class="TLline"><a href="/medgen/7734" ref="tree=MeSH" title="MedGen record for Mucopolysaccharidosis, MPS-II">Mucopolysaccharidosis, MPS-II</a></span></li><li><span class="TLline"><a href="/medgen/19610" ref="tree=MeSH" title="MedGen record for Pyruvate dehydrogenase complex deficiency">Pyruvate dehydrogenase complex deficiency</a></span></li><li><span class="TLline"><a href="/medgen/48441" ref="tree=MeSH" title="MedGen record for Rett syndrome">Rett syndrome</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/10107" ref="tree=MeSH" title="MedGen record for Motor skill disorder">Motor skill disorder</a></span></li><li><span class="TLline"><a href="/medgen/6476" ref="tree=MeSH" title="MedGen record for Mutism">Mutism</a></span><ul><li><span class="TLline"><a href="/medgen/116023" ref="tree=MeSH" title="MedGen record for Selective mutism">Selective mutism</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/39678" ref="tree=MeSH" title="MedGen record for Myelocele">Myelocele</a></span><ul><li><span class="TLline"><a href="/medgen/473138" ref="tree=MeSH" title="MedGen record for Cervical myelocele">Cervical myelocele</a></span></li><li><span class="TLline"><a href="/medgen/473136" ref="tree=MeSH" title="MedGen record for Lumbar myelocele">Lumbar myelocele</a></span></li><li><span class="TLline"><a href="/medgen/476119" ref="tree=MeSH" title="MedGen record for Sacral Myelocele">Sacral Myelocele</a></span></li><li><span class="TLline"><a href="/medgen/473137" ref="tree=MeSH" title="MedGen record for Thoracic myelocele">Thoracic myelocele</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/141906" ref="tree=MeSH" title="MedGen record for reactive attachment disorder">reactive attachment disorder</a></span></li><li><span class="TLline"><a href="/medgen/1999" ref="tree=MeSH" title="MedGen record for Separation anxiety disorder">Separation anxiety disorder</a></span></li><li><span class="TLline"><a href="/medgen/21320" ref="tree=MeSH" title="MedGen record for Stereotypic movement disorder">Stereotypic movement disorder</a></span></li><li><span class="TLline"><a href="/medgen/21556" ref="tree=MeSH" title="MedGen record for Tic">Tic</a></span><ul><li><span class="TLline"><a href="/medgen/21219" ref="tree=MeSH" title="MedGen record for Tourette syndrome">Tourette syndrome</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</div>
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<div class="portlet mgSection" id="ID_105">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
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<div class="nl"><a target="_blank" href="/pubmed/36354027">Tourette syndrome: clinical features, pathophysiology, and treatment.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Johnson KA,
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Worbe Y,
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Foote KD,
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Butson CR,
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Gunduz A,
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Okun MS</span><br />
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<span class="medgenPMjournal">Lancet Neurol</span>
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2023 Feb;22(2):147-158.
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Epub 2022 Oct 28
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doi: 10.1016/S1474-4422(22)00303-9.
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<span class="bold">PMID: </span><a href="/pubmed/36354027" target="_blank">36354027</a><a href="/pmc/articles/PMC10958485" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34174276">Evidence-based pharmacological treatment options for ADHD in children and adolescents.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mechler K,
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Banaschewski T,
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Hohmann S,
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Häge A</span><br />
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<span class="medgenPMjournal">Pharmacol Ther</span>
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2022 Feb;230:107940.
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Epub 2021 Jun 23
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doi: 10.1016/j.pharmthera.2021.107940.
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<span class="bold">PMID: </span><a href="/pubmed/34174276" target="_blank">34174276</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/31843864">Identification, Evaluation, and Management of Children With Autism Spectrum Disorder.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Hyman SL,
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Levy SE,
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Myers SM;
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COUNCIL ON CHILDREN WITH DISABILITIES, SECTION ON DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS</span><br />
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<span class="medgenPMjournal">Pediatrics</span>
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2020 Jan;145(1)
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Epub 2019 Dec 16
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doi: 10.1542/peds.2019-3447.
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<span class="bold">PMID: </span><a href="/pubmed/31843864" target="_blank">31843864</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22neurodevelopmental%20disorder%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (285)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36982559">Neuroinflammation and Oxidative Stress in the Pathogenesis of Autism Spectrum Disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Usui N,
|
||
Kobayashi H,
|
||
Shimada S</span><br />
|
||
<span class="medgenPMjournal">Int J Mol Sci</span>
|
||
2023 Mar 13;24(6)
|
||
doi: 10.3390/ijms24065487.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36982559" target="_blank">36982559</a><a href="/pmc/articles/PMC10049423" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36494048">Innate immune dysfunction and neuroinflammation in autism spectrum disorder (ASD).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hughes HK,
|
||
R J Moreno,
|
||
Ashwood P</span><br />
|
||
<span class="medgenPMjournal">Brain Behav Immun</span>
|
||
2023 Feb;108:245-254.
|
||
Epub 2022 Dec 6
|
||
doi: 10.1016/j.bbi.2022.12.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36494048" target="_blank">36494048</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32662125">Cerebral palsy: Aetiology, pathophysiology and therapeutic interventions.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Upadhyay J,
|
||
Tiwari N,
|
||
Ansari MN</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Pharmacol Physiol</span>
|
||
2020 Dec;47(12):1891-1901.
|
||
Epub 2020 Aug 19
|
||
doi: 10.1111/1440-1681.13379.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32662125" target="_blank">32662125</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31785789">Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Turner TN,
|
||
Wilfert AB,
|
||
Bakken TE,
|
||
Bernier RA,
|
||
Pepper MR,
|
||
Zhang Z,
|
||
Torene RI,
|
||
Retterer K,
|
||
Eichler EE</span><br />
|
||
<span class="medgenPMjournal">Am J Hum Genet</span>
|
||
2019 Dec 5;105(6):1274-1285.
|
||
Epub 2019 Nov 27
|
||
doi: 10.1016/j.ajhg.2019.11.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31785789" target="_blank">31785789</a><a href="/pmc/articles/PMC6904808" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22513218">Developmental dyslexia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Peterson RL,
|
||
Pennington BF</span><br />
|
||
<span class="medgenPMjournal">Lancet</span>
|
||
2012 May 26;379(9830):1997-2007.
|
||
Epub 2012 Apr 17
|
||
doi: 10.1016/S0140-6736(12)60198-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22513218" target="_blank">22513218</a><a href="/pmc/articles/PMC3465717" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neurodevelopmental%20disorder%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (2096)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32977886">Developmental coordination disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Biotteau M,
|
||
Albaret JM,
|
||
Chaix Y</span><br />
|
||
<span class="medgenPMjournal">Handb Clin Neurol</span>
|
||
2020;174:3-20.
|
||
doi: 10.1016/B978-0-444-64148-9.00001-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32977886" target="_blank">32977886</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32699506">Neurodevelopmental disorders-the history and future of a diagnostic concept
.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Morris-Rosendahl DJ,
|
||
Crocq MA</span><br />
|
||
<span class="medgenPMjournal">Dialogues Clin Neurosci</span>
|
||
2020 Mar;22(1):65-72.
|
||
doi: 10.31887/DCNS.2020.22.1/macrocq.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32699506" target="_blank">32699506</a><a href="/pmc/articles/PMC7365295" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32662125">Cerebral palsy: Aetiology, pathophysiology and therapeutic interventions.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Upadhyay J,
|
||
Tiwari N,
|
||
Ansari MN</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Pharmacol Physiol</span>
|
||
2020 Dec;47(12):1891-1901.
|
||
Epub 2020 Aug 19
|
||
doi: 10.1111/1440-1681.13379.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32662125" target="_blank">32662125</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30903299">Autism Spectrum Disorders and ADHD: Overlapping Phenomenology, Diagnostic Issues, and Treatment Considerations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Antshel KM,
|
||
Russo N</span><br />
|
||
<span class="medgenPMjournal">Curr Psychiatry Rep</span>
|
||
2019 Mar 22;21(5):34.
|
||
doi: 10.1007/s11920-019-1020-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30903299" target="_blank">30903299</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29152685">Cerebral Palsy: An Overview.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gulati S,
|
||
Sondhi V</span><br />
|
||
<span class="medgenPMjournal">Indian J Pediatr</span>
|
||
2018 Nov;85(11):1006-1016.
|
||
Epub 2017 Nov 20
|
||
doi: 10.1007/s12098-017-2475-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29152685" target="_blank">29152685</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neurodevelopmental%20disorder%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (2232)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37291210">Trofinetide for the treatment of Rett syndrome: a randomized phase 3 study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Neul JL,
|
||
Percy AK,
|
||
Benke TA,
|
||
Berry-Kravis EM,
|
||
Glaze DG,
|
||
Marsh ED,
|
||
Lin T,
|
||
Stankovic S,
|
||
Bishop KM,
|
||
Youakim JM</span><br />
|
||
<span class="medgenPMjournal">Nat Med</span>
|
||
2023 Jun;29(6):1468-1475.
|
||
Epub 2023 Jun 8
|
||
doi: 10.1038/s41591-023-02398-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37291210" target="_blank">37291210</a><a href="/pmc/articles/PMC10287558" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34174276">Evidence-based pharmacological treatment options for ADHD in children and adolescents.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mechler K,
|
||
Banaschewski T,
|
||
Hohmann S,
|
||
Häge A</span><br />
|
||
<span class="medgenPMjournal">Pharmacol Ther</span>
|
||
2022 Feb;230:107940.
|
||
Epub 2021 Jun 23
|
||
doi: 10.1016/j.pharmthera.2021.107940.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34174276" target="_blank">34174276</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32184147">Iron deficiency in pregnancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Georgieff MK</span><br />
|
||
<span class="medgenPMjournal">Am J Obstet Gynecol</span>
|
||
2020 Oct;223(4):516-524.
|
||
Epub 2020 Mar 14
|
||
doi: 10.1016/j.ajog.2020.03.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32184147" target="_blank">32184147</a><a href="/pmc/articles/PMC7492370" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31876938">Nutritional interventions for autism spectrum disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Karhu E,
|
||
Zukerman R,
|
||
Eshraghi RS,
|
||
Mittal J,
|
||
Deth RC,
|
||
Castejon AM,
|
||
Trivedi M,
|
||
Mittal R,
|
||
Eshraghi AA</span><br />
|
||
<span class="medgenPMjournal">Nutr Rev</span>
|
||
2020 Jul 1;78(7):515-531.
|
||
doi: 10.1093/nutrit/nuz092.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31876938" target="_blank">31876938</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26386541">Attention deficit hyperactivity disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Thapar A,
|
||
Cooper M</span><br />
|
||
<span class="medgenPMjournal">Lancet</span>
|
||
2016 Mar 19;387(10024):1240-50.
|
||
Epub 2015 Sep 17
|
||
doi: 10.1016/S0140-6736(15)00238-X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26386541" target="_blank">26386541</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neurodevelopmental%20disorder%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (734)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38574728">Infant microbes and metabolites point to childhood neurodevelopmental disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ahrens AP,
|
||
Hyötyläinen T,
|
||
Petrone JR,
|
||
Igelström K,
|
||
George CD,
|
||
Garrett TJ,
|
||
Orešič M,
|
||
Triplett EW,
|
||
Ludvigsson J</span><br />
|
||
<span class="medgenPMjournal">Cell</span>
|
||
2024 Apr 11;187(8):1853-1873.e15.
|
||
Epub 2024 Apr 3
|
||
doi: 10.1016/j.cell.2024.02.035.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38574728" target="_blank">38574728</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29330883">Genotype-phenotype correlations in individuals with pathogenic RERE variants.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jordan VK,
|
||
Fregeau B,
|
||
Ge X,
|
||
Giordano J,
|
||
Wapner RJ,
|
||
Balci TB,
|
||
Carter MT,
|
||
Bernat JA,
|
||
Moccia AN,
|
||
Srivastava A,
|
||
Martin DM,
|
||
Bielas SL,
|
||
Pappas J,
|
||
Svoboda MD,
|
||
Rio M,
|
||
Boddaert N,
|
||
Cantagrel V,
|
||
Lewis AM,
|
||
Scaglia F;
|
||
Undiagnosed Diseases Network,
|
||
Kohler JN,
|
||
Bernstein JA,
|
||
Dries AM,
|
||
Rosenfeld JA,
|
||
DeFilippo C,
|
||
Thorson W,
|
||
Yang Y,
|
||
Sherr EH,
|
||
Bi W,
|
||
Scott DA</span><br />
|
||
<span class="medgenPMjournal">Hum Mutat</span>
|
||
2018 May;39(5):666-675.
|
||
Epub 2018 Jan 25
|
||
doi: 10.1002/humu.23400.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29330883" target="_blank">29330883</a><a href="/pmc/articles/PMC5903952" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29152685">Cerebral Palsy: An Overview.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gulati S,
|
||
Sondhi V</span><br />
|
||
<span class="medgenPMjournal">Indian J Pediatr</span>
|
||
2018 Nov;85(11):1006-1016.
|
||
Epub 2017 Nov 20
|
||
doi: 10.1007/s12098-017-2475-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29152685" target="_blank">29152685</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28472621">The valproic acid-induced rodent model of autism.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nicolini C,
|
||
Fahnestock M</span><br />
|
||
<span class="medgenPMjournal">Exp Neurol</span>
|
||
2018 Jan;299(Pt A):217-227.
|
||
Epub 2017 May 2
|
||
doi: 10.1016/j.expneurol.2017.04.017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28472621" target="_blank">28472621</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26386541">Attention deficit hyperactivity disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Thapar A,
|
||
Cooper M</span><br />
|
||
<span class="medgenPMjournal">Lancet</span>
|
||
2016 Mar 19;387(10024):1240-50.
|
||
Epub 2015 Sep 17
|
||
doi: 10.1016/S0140-6736(15)00238-X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26386541" target="_blank">26386541</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neurodevelopmental%20disorder%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (855)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38453051">Penetrance, variable expressivity and monogenic neurodevelopmental disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">de Masfrand S,
|
||
Cogné B,
|
||
Nizon M,
|
||
Deb W,
|
||
Goldenberg A,
|
||
Lecoquierre F,
|
||
Nicolas G,
|
||
Bournez M,
|
||
Vitobello A,
|
||
Mau-Them FT,
|
||
le Guyader G,
|
||
Bilan F,
|
||
Bauer P,
|
||
Zweier C,
|
||
Piard J,
|
||
Pasquier L,
|
||
Bézieau S,
|
||
Gerard B,
|
||
Faivre L,
|
||
Saugier-Veber P,
|
||
Piton A,
|
||
Isidor B</span><br />
|
||
<span class="medgenPMjournal">Eur J Med Genet</span>
|
||
2024 Jun;69:104932.
|
||
Epub 2024 Mar 5
|
||
doi: 10.1016/j.ejmg.2024.104932.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38453051" target="_blank">38453051</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32977886">Developmental coordination disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Biotteau M,
|
||
Albaret JM,
|
||
Chaix Y</span><br />
|
||
<span class="medgenPMjournal">Handb Clin Neurol</span>
|
||
2020;174:3-20.
|
||
doi: 10.1016/B978-0-444-64148-9.00001-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32977886" target="_blank">32977886</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32730804">Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fliedner A,
|
||
Kirchner P,
|
||
Wiesener A,
|
||
van de Beek I,
|
||
Waisfisz Q,
|
||
van Haelst M,
|
||
Scott DA,
|
||
Lalani SR,
|
||
Rosenfeld JA,
|
||
Azamian MS,
|
||
Xia F,
|
||
Dutra-Clarke M,
|
||
Martinez-Agosto JA,
|
||
Lee H;
|
||
UCLA Clinical Genomics Center,
|
||
Noh GJ,
|
||
Lippa N,
|
||
Alkelai A,
|
||
Aggarwal V,
|
||
Agre KE,
|
||
Gavrilova R,
|
||
Mirzaa GM,
|
||
Straussberg R,
|
||
Cohen R,
|
||
Horist B,
|
||
Krishnamurthy V,
|
||
McWalter K,
|
||
Juusola J,
|
||
Davis-Keppen L,
|
||
Ohden L,
|
||
van Slegtenhorst M,
|
||
de Man SA,
|
||
Ekici AB,
|
||
Gregor A,
|
||
van de Laar I,
|
||
Zweier C</span><br />
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<span class="medgenPMjournal">Am J Hum Genet</span>
|
||
2020 Sep 3;107(3):544-554.
|
||
Epub 2020 Jul 29
|
||
doi: 10.1016/j.ajhg.2020.06.019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32730804" target="_blank">32730804</a><a href="/pmc/articles/PMC7477272" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32699506">Neurodevelopmental disorders-the history and future of a diagnostic concept
.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Morris-Rosendahl DJ,
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||
Crocq MA</span><br />
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||
<span class="medgenPMjournal">Dialogues Clin Neurosci</span>
|
||
2020 Mar;22(1):65-72.
|
||
doi: 10.31887/DCNS.2020.22.1/macrocq.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32699506" target="_blank">32699506</a><a href="/pmc/articles/PMC7365295" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31059731">Behavioral neuroscience of autism.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Takumi T,
|
||
Tamada K,
|
||
Hatanaka F,
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||
Nakai N,
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||
Bolton PF</span><br />
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<span class="medgenPMjournal">Neurosci Biobehav Rev</span>
|
||
2020 Mar;110:60-76.
|
||
Epub 2019 May 3
|
||
doi: 10.1016/j.neubiorev.2019.04.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31059731" target="_blank">31059731</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neurodevelopmental%20disorder%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1815)</a></div></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="nl"><a target="_blank" href="/pubmed/36642718">Global prevalence of Rett syndrome: systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Petriti U,
|
||
Dudman DC,
|
||
Scosyrev E,
|
||
Lopez-Leon S</span><br />
|
||
<span class="medgenPMjournal">Syst Rev</span>
|
||
2023 Jan 16;12(1):5.
|
||
doi: 10.1186/s13643-023-02169-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36642718" target="_blank">36642718</a><a href="/pmc/articles/PMC9841621" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34043900">Cannabis and cannabinoid use in autism spectrum disorder: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Silva EAD Junior,
|
||
Medeiros WMB,
|
||
Torro N,
|
||
Sousa JMM,
|
||
Almeida IBCM,
|
||
Costa FBD,
|
||
Pontes KM,
|
||
Nunes ELG,
|
||
Rosa MDD,
|
||
Albuquerque KLGD</span><br />
|
||
<span class="medgenPMjournal">Trends Psychiatry Psychother</span>
|
||
2022 Jun 13;44:e20200149.
|
||
doi: 10.47626/2237-6089-2020-0149.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34043900" target="_blank">34043900</a><a href="/pmc/articles/PMC9887656" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31629998">Non-pharmacological interventions for cognitive difficulties in ADHD: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lambez B,
|
||
Harwood-Gross A,
|
||
Golumbic EZ,
|
||
Rassovsky Y</span><br />
|
||
<span class="medgenPMjournal">J Psychiatr Res</span>
|
||
2020 Jan;120:40-55.
|
||
Epub 2019 Oct 12
|
||
doi: 10.1016/j.jpsychires.2019.10.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31629998" target="_blank">31629998</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28602046">Exercise interventions for cerebral palsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ryan JM,
|
||
Cassidy EE,
|
||
Noorduyn SG,
|
||
O'Connell NE</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2017 Jun 11;6(6):CD011660.
|
||
doi: 10.1002/14651858.CD011660.pub2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28602046" target="_blank">28602046</a><a href="/pmc/articles/PMC6481791" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26040902">Omega-3 polyunsaturated fatty acid supplementation and cognition: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cooper RE,
|
||
Tye C,
|
||
Kuntsi J,
|
||
Vassos E,
|
||
Asherson P</span><br />
|
||
<span class="medgenPMjournal">J Psychopharmacol</span>
|
||
2015 Jul;29(7):753-63.
|
||
Epub 2015 Jun 3
|
||
doi: 10.1177/0269881115587958.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26040902" target="_blank">26040902</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Neurodevelopmental%20disorder%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (168)</a></div></div>
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