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<meta name="keywords" content="C0454642, developmental receptive language delay, finding, mental or behavioral dysfunction, receptive developmental language delay, receptive language delay, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="A delay in the acquisition of the ability to understand the speech of others." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=451061
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ConceptID=C0454642
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Receptive language delay</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>451061</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."><span class="highlight" style="background-color:">C0454642</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding; Mental or Behavioral Dysfunction</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Developmental receptive language delay; Receptive developmental language delay</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Developmental receptive language delay (229736005); Receptive developmental language delay (229736005); Receptive language delay (229736005)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0010863">HP:0010863</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>
|
||
<div class="portlet_content ln">A delay in the acquisition of the ability to understand the speech of others. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
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</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="TLline">Receptive language delay</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/868417" ref="tree=MeSH" title="MedGen record for Abnormal nervous system physiology">Abnormal nervous system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/868343" ref="tree=MeSH" title="MedGen record for Neurodevelopmental abnormality">Neurodevelopmental abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/868344" ref="tree=MeSH" title="MedGen record for Neurodevelopmental delay">Neurodevelopmental delay</a></span><ul><li><span class="TLline"><a href="/medgen/105318" ref="tree=MeSH" title="MedGen record for Delayed speech and language development">Delayed speech and language development</a></span><ul><li><span class="matched_ds">Receptive language delay</span><ul><li><span class="TLline"><a href="/medgen/1853252" ref="tree=MeSH" title="MedGen record for Delayed spoken language comprehension">Delayed spoken language comprehension</a></span></li><li><span class="TLline"><a href="/medgen/504297" ref="tree=MeSH" title="MedGen record for Mild receptive language delay">Mild receptive language delay</a></span></li><li><span class="TLline"><a href="/medgen/504295" ref="tree=MeSH" title="MedGen record for Moderate receptive language delay">Moderate receptive language delay</a></span></li><li><span class="TLline"><a href="/medgen/504296" ref="tree=MeSH" title="MedGen record for Severe receptive language delay">Severe receptive language delay</a></span></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_112">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_413258"><div><strong>Cortical dysplasia-focal epilepsy syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>413258</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.">C2750246</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Pitt-Hopkins-like syndrome-1 (PTHSL1) is an autosomal recessive neurodevelopmental disorder characterized by delayed psychomotor development, intellectual disability, severe speech impairment or regression, and behavioral abnormalities. Most patients have onset of seizures within the first years of life. Some patients may have cortical dysplasia on brain imaging (summary by Smogavec et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/413258">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_444010"><div><strong>Potocki-Lupski syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>444010</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.">C2931246</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Potocki-Lupski syndrome (PTLS) is characterized by cognitive, behavioral, and medical manifestations. Cognitively, most individuals present with developmental delay, later meeting criteria for moderate intellectual disability. Behaviorally, issues with attention, hyperactivity, withdrawal, and anxiety may be seen. Some individuals meet criteria for autism spectrum disorder. Medically, hypotonia, oropharyngeal dysphagia leading to failure to thrive, congenital heart disease, hypoglycemia associated with growth hormone deficiency, and mildly dysmorphic facial features are observed. Medical manifestations typically lead to identification of PTLS in infancy; however, those with only behavioral and cognitive manifestations may be identified in later childhood.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/444010">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_906099"><div><strong>Chromosome 10q23 deletion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>906099</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.">C4225669</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The 10q22.3-q23.2 region is characterized by a complex set of low-copy repeats (LCRs), which can give rise to various genomic changes mediated by nonallelic homologous recombination (NAHR). Recurrent deletions of chromosome 10q22.3-q23.2, including the BMPR1A gene (601299) have been associated with dysmorphic facies, developmental delay, and multiple congenital anomalies. Some patients with deletions that extend distally to include the PTEN gene (601728) have a more severe phenotype with infantile/juvenile polyposis, macrocephaly, dysmorphic facial features, and developmental delay (summary by van Bon et al., 2011).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/906099">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1648339"><div><strong>Intellectual developmental disorder with macrocephaly, seizures, and speech delay</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1648339</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.">C4748428</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">IDDMSSD is a neurodevelopmental disorder characterized by impaired intellectual development, poor speech, postnatal macrocephaly, and seizures (Harms et al., 2018).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1648339">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1762595"><div><strong>Lessel-Kreienkamp syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1762595</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.">C5436892</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Lessel-Kreienkamp syndrome (LESKRES) is a neurodevelopmental disorder characterized by global developmental delay with intellectual disability and speech and language delay apparent from infancy or early childhood. The severity of the disorder is highly variable: some patients have mildly delayed walking and mild cognitive deficits, whereas others are nonambulatory and nonverbal. Most have behavioral disorders. Additional features, including seizures, hypotonia, gait abnormalities, visual defects, cardiac defects, and nonspecific dysmorphic facial features, may also be present (summary by Lessel et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1762595">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1840909"><div><strong>Neurodevelopmental disorder with poor growth and behavioral abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1840909</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.">C5830273</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with poor growth and behavioral abnormalities (NEDGBA) is an autosomal recessive disorder characterized by global developmental delay, moderately to severely impaired intellectual development, often with absent speech, and behavioral abnormalities, including hyperactivity, short attention span, and ADHD. Affected individuals show failure to thrive with poor overall growth; some have microcephaly. Additional features may include nonspecific facial dysmorphism, hypotonia, and feeding difficulties (Vogt et al., 2022; Meng et al., 2023).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1840909">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1845825"><div><strong>Alfadhel syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1845825</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.">C5882735</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Alfadhel syndrome (AFDL) is an autosomal recessive neurodevelopmental disorder with features of global developmental delay, hypotonia, and facial dysmorphism (Asiri et al., 2020, Bertoli-Avella et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1845825">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1845825" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Alfadhel syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_906099" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chromosome 10q23 deletion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_413258" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cortical dysplasia-focal epilepsy syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1648339" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual developmental disorder with macrocephaly, seizures, and speech delay</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1762595" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lessel-Kreienkamp syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1840909" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with poor growth and behavioral abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_444010" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Potocki-Lupski syndrome</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<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>
|
||
<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>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38377329">Clinical practice guideline: Interventions for Developmental Language Delay and Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Neumann K,
|
||
Kauschke C,
|
||
Fox-Boyer A,
|
||
Lüke C,
|
||
Sallat S,
|
||
Kiese-Himmel C</span><br />
|
||
<span class="medgenPMjournal">Dtsch Arztebl Int</span>
|
||
2024 Mar 8;121(5):155-162.
|
||
doi: 10.3238/arztebl.m2024.0004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38377329" target="_blank">38377329</a><a href="/pmc/articles/PMC11539890" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38050025">Health supervision for children and adolescents with 16p11.2 deletion syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chung WK,
|
||
Herrera FF;
|
||
Simon's Searchlight Foundation</span><br />
|
||
<span class="medgenPMjournal">Cold Spring Harb Mol Case Stud</span>
|
||
2023 Dec;9(4)
|
||
Epub 2024 Jan 10
|
||
doi: 10.1101/mcs.a006316.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38050025" target="_blank">38050025</a><a href="/pmc/articles/PMC10815286" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29173721">An Interprofessional Team Approach to the Differential Diagnosis of Children with Language Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu XL,
|
||
Zahrt DM,
|
||
Simms MD</span><br />
|
||
<span class="medgenPMjournal">Pediatr Clin North Am</span>
|
||
2018 Feb;65(1):73-90.
|
||
doi: 10.1016/j.pcl.2017.08.022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29173721" target="_blank">29173721</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22receptive%20language%20delay%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 (5)</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/38377329">Clinical practice guideline: Interventions for Developmental Language Delay and Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Neumann K,
|
||
Kauschke C,
|
||
Fox-Boyer A,
|
||
Lüke C,
|
||
Sallat S,
|
||
Kiese-Himmel C</span><br />
|
||
<span class="medgenPMjournal">Dtsch Arztebl Int</span>
|
||
2024 Mar 8;121(5):155-162.
|
||
doi: 10.3238/arztebl.m2024.0004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38377329" target="_blank">38377329</a><a href="/pmc/articles/PMC11539890" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30348077">Language delay aggregates in toddler siblings of children with autism spectrum disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marrus N,
|
||
Hall LP,
|
||
Paterson SJ,
|
||
Elison JT,
|
||
Wolff JJ,
|
||
Swanson MR,
|
||
Parish-Morris J,
|
||
Eggebrecht AT,
|
||
Pruett JR Jr,
|
||
Hazlett HC,
|
||
Zwaigenbaum L,
|
||
Dager S,
|
||
Estes AM,
|
||
Schultz RT,
|
||
Botteron KN,
|
||
Piven J,
|
||
Constantino JN;
|
||
IBIS Network</span><br />
|
||
<span class="medgenPMjournal">J Neurodev Disord</span>
|
||
2018 Oct 22;10(1):29.
|
||
doi: 10.1186/s11689-018-9247-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30348077" target="_blank">30348077</a><a href="/pmc/articles/PMC6198516" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29786137">Longitudinal growth of receptive language in children with cerebral palsy between 18 months and 54 months of age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hustad KC,
|
||
Sakash A,
|
||
Broman AT,
|
||
Rathouz PJ</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2018 Nov;60(11):1156-1164.
|
||
Epub 2018 May 22
|
||
doi: 10.1111/dmcn.13904.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29786137" target="_blank">29786137</a><a href="/pmc/articles/PMC6175617" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25955535">Language outcomes among ELBW infants in early childhood.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adams-Chapman I,
|
||
Bann C,
|
||
Carter SL,
|
||
Stoll BJ;
|
||
NICHD Neonatal Research Network</span><br />
|
||
<span class="medgenPMjournal">Early Hum Dev</span>
|
||
2015 Jun;91(6):373-9.
|
||
Epub 2015 May 4
|
||
doi: 10.1016/j.earlhumdev.2015.03.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25955535" target="_blank">25955535</a><a href="/pmc/articles/PMC4442021" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23362033">Late talkers: do good predictors of outcome exist?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rescorla L</span><br />
|
||
<span class="medgenPMjournal">Dev Disabil Res Rev</span>
|
||
2011;17(2):141-50.
|
||
doi: 10.1002/ddrr.1108.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23362033" target="_blank">23362033</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Receptive%20language%20delay%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 (16)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38377329">Clinical practice guideline: Interventions for Developmental Language Delay and Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Neumann K,
|
||
Kauschke C,
|
||
Fox-Boyer A,
|
||
Lüke C,
|
||
Sallat S,
|
||
Kiese-Himmel C</span><br />
|
||
<span class="medgenPMjournal">Dtsch Arztebl Int</span>
|
||
2024 Mar 8;121(5):155-162.
|
||
doi: 10.3238/arztebl.m2024.0004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38377329" target="_blank">38377329</a><a href="/pmc/articles/PMC11539890" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30348077">Language delay aggregates in toddler siblings of children with autism spectrum disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marrus N,
|
||
Hall LP,
|
||
Paterson SJ,
|
||
Elison JT,
|
||
Wolff JJ,
|
||
Swanson MR,
|
||
Parish-Morris J,
|
||
Eggebrecht AT,
|
||
Pruett JR Jr,
|
||
Hazlett HC,
|
||
Zwaigenbaum L,
|
||
Dager S,
|
||
Estes AM,
|
||
Schultz RT,
|
||
Botteron KN,
|
||
Piven J,
|
||
Constantino JN;
|
||
IBIS Network</span><br />
|
||
<span class="medgenPMjournal">J Neurodev Disord</span>
|
||
2018 Oct 22;10(1):29.
|
||
doi: 10.1186/s11689-018-9247-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30348077" target="_blank">30348077</a><a href="/pmc/articles/PMC6198516" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29786137">Longitudinal growth of receptive language in children with cerebral palsy between 18 months and 54 months of age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hustad KC,
|
||
Sakash A,
|
||
Broman AT,
|
||
Rathouz PJ</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2018 Nov;60(11):1156-1164.
|
||
Epub 2018 May 22
|
||
doi: 10.1111/dmcn.13904.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29786137" target="_blank">29786137</a><a href="/pmc/articles/PMC6175617" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29173721">An Interprofessional Team Approach to the Differential Diagnosis of Children with Language Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu XL,
|
||
Zahrt DM,
|
||
Simms MD</span><br />
|
||
<span class="medgenPMjournal">Pediatr Clin North Am</span>
|
||
2018 Feb;65(1):73-90.
|
||
doi: 10.1016/j.pcl.2017.08.022.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29173721" target="_blank">29173721</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23362033">Late talkers: do good predictors of outcome exist?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rescorla L</span><br />
|
||
<span class="medgenPMjournal">Dev Disabil Res Rev</span>
|
||
2011;17(2):141-50.
|
||
doi: 10.1002/ddrr.1108.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23362033" target="_blank">23362033</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Receptive%20language%20delay%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 (13)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37408377">Heterogeneity of autism symptoms in community-referred infants and toddlers at elevated or low familial likelihood of autism.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cohenour TL,
|
||
Gulsrud A,
|
||
Kasari C</span><br />
|
||
<span class="medgenPMjournal">Autism Res</span>
|
||
2023 Sep;16(9):1739-1749.
|
||
Epub 2023 Jul 5
|
||
doi: 10.1002/aur.2973.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37408377" target="_blank">37408377</a><a href="/pmc/articles/PMC10527623" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23586418">Spatial hearing in a child with auditory neuropathy spectrum disorder and bilateral cochlear implants.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Johnstone PM,
|
||
Yeager KR,
|
||
Noss E</span><br />
|
||
<span class="medgenPMjournal">Int J Audiol</span>
|
||
2013 Jun;52(6):400-8.
|
||
Epub 2013 Apr 16
|
||
doi: 10.3109/14992027.2013.779755.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23586418" target="_blank">23586418</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9290609">Sensitivity and specificity of the neonatal brain-stem auditory evoked potential for hearing and language deficits in survivors of extracorporeal membrane oxygenation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Desai S,
|
||
Kollros PR,
|
||
Graziani LJ,
|
||
Streletz LJ,
|
||
Goodman M,
|
||
Stanley C,
|
||
Cullen J,
|
||
Baumgart S</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
1997 Aug;131(2):233-9.
|
||
doi: 10.1016/s0022-3476(97)70159-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9290609" target="_blank">9290609</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Receptive%20language%20delay%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 (3)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35090718">Risk stratification helps identify congenital diaphragmatic hernia (CDH) infants in need of formal neurodevelopmental assessment: Observations from a structured, interdisciplinary long-term follow-up clinic.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hassan M,
|
||
Patel D,
|
||
LaRusso K,
|
||
Koclas L,
|
||
Smith-Morin Ot M,
|
||
Shapiro AJ,
|
||
Sant'Anna A,
|
||
Altit G,
|
||
Beauseigle S,
|
||
Puligandla PS</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Surg</span>
|
||
2022 May;57(5):846-850.
|
||
Epub 2022 Jan 13
|
||
doi: 10.1016/j.jpedsurg.2021.12.048.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35090718" target="_blank">35090718</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29786137">Longitudinal growth of receptive language in children with cerebral palsy between 18 months and 54 months of age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hustad KC,
|
||
Sakash A,
|
||
Broman AT,
|
||
Rathouz PJ</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2018 Nov;60(11):1156-1164.
|
||
Epub 2018 May 22
|
||
doi: 10.1111/dmcn.13904.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29786137" target="_blank">29786137</a><a href="/pmc/articles/PMC6175617" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25955535">Language outcomes among ELBW infants in early childhood.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adams-Chapman I,
|
||
Bann C,
|
||
Carter SL,
|
||
Stoll BJ;
|
||
NICHD Neonatal Research Network</span><br />
|
||
<span class="medgenPMjournal">Early Hum Dev</span>
|
||
2015 Jun;91(6):373-9.
|
||
Epub 2015 May 4
|
||
doi: 10.1016/j.earlhumdev.2015.03.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25955535" target="_blank">25955535</a><a href="/pmc/articles/PMC4442021" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23362033">Late talkers: do good predictors of outcome exist?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rescorla L</span><br />
|
||
<span class="medgenPMjournal">Dev Disabil Res Rev</span>
|
||
2011;17(2):141-50.
|
||
doi: 10.1002/ddrr.1108.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23362033" target="_blank">23362033</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18757840">Managing referrals for children with receptive language delay.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fagan MK,
|
||
Montgomery TR</span><br />
|
||
<span class="medgenPMjournal">Clin Pediatr (Phila)</span>
|
||
2009 Jan;48(1):72-80.
|
||
Epub 2008 Aug 29
|
||
doi: 10.1177/0009922808323108.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18757840" target="_blank">18757840</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Receptive%20language%20delay%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 (10)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37263801">Clinical case report: mosaic ANK3 pathogenic variant in a patient with autism spectrum disorder and neurodevelopmental delay.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fang X,
|
||
Fee T,
|
||
Davis J,
|
||
Stolerman ES,
|
||
Caylor RC</span><br />
|
||
<span class="medgenPMjournal">Cold Spring Harb Mol Case Stud</span>
|
||
2023 Jun;9(3)
|
||
Epub 2023 Jul 11
|
||
doi: 10.1101/mcs.a006233.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37263801" target="_blank">37263801</a><a href="/pmc/articles/PMC10393183" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30348077">Language delay aggregates in toddler siblings of children with autism spectrum disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marrus N,
|
||
Hall LP,
|
||
Paterson SJ,
|
||
Elison JT,
|
||
Wolff JJ,
|
||
Swanson MR,
|
||
Parish-Morris J,
|
||
Eggebrecht AT,
|
||
Pruett JR Jr,
|
||
Hazlett HC,
|
||
Zwaigenbaum L,
|
||
Dager S,
|
||
Estes AM,
|
||
Schultz RT,
|
||
Botteron KN,
|
||
Piven J,
|
||
Constantino JN;
|
||
IBIS Network</span><br />
|
||
<span class="medgenPMjournal">J Neurodev Disord</span>
|
||
2018 Oct 22;10(1):29.
|
||
doi: 10.1186/s11689-018-9247-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30348077" target="_blank">30348077</a><a href="/pmc/articles/PMC6198516" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29786137">Longitudinal growth of receptive language in children with cerebral palsy between 18 months and 54 months of age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hustad KC,
|
||
Sakash A,
|
||
Broman AT,
|
||
Rathouz PJ</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2018 Nov;60(11):1156-1164.
|
||
Epub 2018 May 22
|
||
doi: 10.1111/dmcn.13904.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29786137" target="_blank">29786137</a><a href="/pmc/articles/PMC6175617" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25955535">Language outcomes among ELBW infants in early childhood.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adams-Chapman I,
|
||
Bann C,
|
||
Carter SL,
|
||
Stoll BJ;
|
||
NICHD Neonatal Research Network</span><br />
|
||
<span class="medgenPMjournal">Early Hum Dev</span>
|
||
2015 Jun;91(6):373-9.
|
||
Epub 2015 May 4
|
||
doi: 10.1016/j.earlhumdev.2015.03.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25955535" target="_blank">25955535</a><a href="/pmc/articles/PMC4442021" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23362033">Late talkers: do good predictors of outcome exist?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rescorla L</span><br />
|
||
<span class="medgenPMjournal">Dev Disabil Res Rev</span>
|
||
2011;17(2):141-50.
|
||
doi: 10.1002/ddrr.1108.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23362033" target="_blank">23362033</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Receptive%20language%20delay%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 (11)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
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||
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|
||
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|
||
|
||
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|
||
|
||
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|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
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|
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|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Receptive%20language%20delay" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22receptive%20language%20delay%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">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Receptive%20language%20delay" target="_blank">MedlinePlus</a></li></ul></div>
|
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|
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|
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|
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<a href="/pubmed/clinical?term=Receptive%20language%20delay" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Receptive%20language%20delay%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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<li class="brieflinkpopper">
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<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=451061" ref="log$=recordlinks">ClinVar</a>
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<div class="brieflinkpop offscreen_noflow">Related medical variations</div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d0b813f4a390645ecd150f">Receptive language delay</a>
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<div class="ralinkpop offscreen_noflow">Receptive language delay<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d0b811b15b832ebca63293">C0034194[trait identifier] AND "Talkowski Laboratory, Center for ... <span class="number">(1)</span></a>
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<div class="ralinkpop offscreen_noflow">C0034194[trait identifier] AND "Talkowski Laboratory, Center for Human Genetic Research, Massachusetts General Hospital"[submitter]<div class="brieflinkpopdesc">Search</div></div>
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<div class="tertiary">ClinVar</div>
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<a class="htb" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d0b81184f3725e59cad9e9">C0454642[conceptid] <span class="number">(1)</span></a>
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