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<meta name="keywords" content="C2711610, abnormal brain imaging, abnormalities on brain imaging, brain abnormalities on imaging, brain imaging abnormalities, brain imaging abnormality, finding, imaging of brain abnormal, 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="An anomaly of metabolism or structure of the brain identified by imaging." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=751376
|
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ConceptID=C2711610
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Brain imaging abnormality</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>751376</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:">C2711610</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Abnormal brain imaging; Abnormalities on brain imaging; Brain abnormalities on imaging; Brain imaging abnormalities</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Imaging of brain abnormal (442731005)</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:0410263">HP:0410263</a></td></tr>
|
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</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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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">An anomaly of metabolism or structure of the brain identified by imaging. [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>
|
||
<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">Brain imaging abnormality</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/871309" ref="tree=MeSH" title="MedGen record for Abnormality of prenatal development or birth">Abnormality of prenatal development or birth</a></span><ul><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span><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="matched_ds">Brain imaging abnormality</span><ul><li><span class="TLline"><a href="/medgen/868405" ref="tree=MeSH" title="MedGen record for Abnormal brain positron emission tomography">Abnormal brain positron emission tomography</a></span><ul><li><span class="TLline"><a href="/medgen/868404" ref="tree=MeSH" title="MedGen record for Abnormal brain FDG positron emission tomography">Abnormal brain FDG positron emission tomography</a></span><ul><li><span class="TLline"><a href="/medgen/868401" ref="tree=MeSH" title="MedGen record for Hypothalamic hypometabolism in FDG PET">Hypothalamic hypometabolism in FDG PET</a></span></li><li><span class="TLline"><a href="/medgen/868400" ref="tree=MeSH" title="MedGen record for Parietal hypometabolism in FDG PET">Parietal hypometabolism in FDG PET</a></span></li><li><span class="TLline"><a href="/medgen/868403" ref="tree=MeSH" title="MedGen record for Prefrontal hypometabolism in FDG PET">Prefrontal hypometabolism in FDG PET</a></span></li><li><span class="TLline"><a href="/medgen/868402" ref="tree=MeSH" title="MedGen record for Thalamic hypometabolism in FDG PET">Thalamic hypometabolism in FDG PET</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/868370" ref="tree=MeSH" title="MedGen record for Abnormal metabolic brain imaging by MRS">Abnormal metabolic brain imaging by MRS</a></span><ul><li><span class="TLline"><a href="/medgen/1369027" ref="tree=MeSH" title="MedGen record for Abnormal brain choline level by MRS">Abnormal brain choline level by MRS</a></span><ul><li><span class="TLline"><a href="/medgen/868369" ref="tree=MeSH" title="MedGen record for Elevated brain choline level by MRS">Elevated brain choline level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1371032" ref="tree=MeSH" title="MedGen record for Reduced brain choline level by MRS">Reduced brain choline level by MRS</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/868366" ref="tree=MeSH" title="MedGen record for Abnormal brain choline/creatine ratio by MRS">Abnormal brain choline/creatine ratio by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1370529" ref="tree=MeSH" title="MedGen record for Abnormal brain creatine level by MRS">Abnormal brain creatine level by MRS</a></span><ul><li><span class="TLline"><a href="/medgen/1370595" ref="tree=MeSH" title="MedGen record for Elevated brain creatine level by MRS">Elevated brain creatine level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1369880" ref="tree=MeSH" title="MedGen record for Reduced brain creatine level by MRS">Reduced brain creatine level by MRS</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1841685" ref="tree=MeSH" title="MedGen record for Abnormal brain glutamine level by MRS">Abnormal brain glutamine level by MRS</a></span><ul><li><span class="TLline"><a href="/medgen/1841826" ref="tree=MeSH" title="MedGen record for Elevated brain glutamine level by MRS">Elevated brain glutamine level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1393827" ref="tree=MeSH" title="MedGen record for Reduced brain glutamine level by MRS">Reduced brain glutamine level by MRS</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1369712" ref="tree=MeSH" title="MedGen record for Abnormal brain lactate level by MRS">Abnormal brain lactate level by MRS</a></span><ul><li><span class="TLline"><a href="/medgen/868368" ref="tree=MeSH" title="MedGen record for Elevated brain lactate level by MRS">Elevated brain lactate level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1370976" ref="tree=MeSH" title="MedGen record for Reduced brain lactate level by MRS">Reduced brain lactate level by MRS</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1370991" ref="tree=MeSH" title="MedGen record for Abnormal brain N-acetyl aspartate level by MRS">Abnormal brain N-acetyl aspartate level by MRS</a></span><ul><li><span class="TLline"><a href="/medgen/1369723" ref="tree=MeSH" title="MedGen record for Elevated brain N-acetyl aspartate level by MRS">Elevated brain N-acetyl aspartate level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/868367" ref="tree=MeSH" title="MedGen record for Reduced brain N-acetyl aspartate level by MRS">Reduced brain N-acetyl aspartate level by MRS</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1841957" ref="tree=MeSH" title="MedGen record for Elevated brain gamma-aminobutyric acid by MRS">Elevated brain gamma-aminobutyric acid by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1842032" ref="tree=MeSH" title="MedGen record for Elevated brain glycine level by MRS">Elevated brain glycine level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1864179" ref="tree=MeSH" title="MedGen record for Elevated brain guanidinoacetate level by MRS">Elevated brain guanidinoacetate level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1841987" ref="tree=MeSH" title="MedGen record for Elevated brain polyol compounds by MRS">Elevated brain polyol compounds by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1054512" ref="tree=MeSH" title="MedGen record for Elevated brain succinate level by MRS">Elevated brain succinate level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1863563" ref="tree=MeSH" title="MedGen record for Elevated methylhex-dienedioic level by MRS">Elevated methylhex-dienedioic level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1382727" ref="tree=MeSH" title="MedGen record for High myoinositol in brain by MRS">High myoinositol in brain by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1382756" ref="tree=MeSH" title="MedGen record for Reduced brain gamma-aminobutyric acid level by MRS">Reduced brain gamma-aminobutyric acid level by MRS</a></span></li><li><span class="TLline"><a href="/medgen/1380742" ref="tree=MeSH" title="MedGen record for Reduced brain glutamate level by MRS">Reduced brain glutamate level by MRS</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
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||
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||
<div class="portlet mgSection" id="ID_112">
|
||
<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>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_481914"><div><strong>Intellectual disability, autosomal dominant 10</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>481914</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.">C3280284</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CACNG2 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/481914">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_903483"><div><strong>Acrofacial dysostosis Cincinnati type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>903483</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.">C4225317</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The Cincinnati type of acrofacial dysostosis is a ribosomopathy characterized by a spectrum of mandibulofacial dysostosis phenotypes, with or without extrafacial skeletal defects (Weaver et al., 2015). In addition, a significant number of neurologic abnormalities have been reported, ranging from mild delays to refractory epilepsy, as well as an increased incidence of congenital heart defects, primarily septal in nature (Smallwood et al., 2023).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/903483">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934745"><div><strong>TELO2-related intellectual disability-neurodevelopmental disorder</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934745</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.">C4310778</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">You-Hoover-Fong syndrome (YHFS) is an autosomal recessive disorder with clinical features of global developmental delay, impaired intellectual development, dysmorphic facial features, microcephaly, abnormal movements, and abnormal auditory and visual function (You et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934745">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1623077"><div><strong>Facial palsy, congenital, with ptosis and velopharyngeal dysfunction</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1623077</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.">C4540277</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1623077">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1672912"><div><strong>Neurodevelopmental disorder with seizures and speech and walking impairment</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1672912</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.">C5193119</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with seizures and speech and walking impairment (NEDSSWI) is an autosomal recessive disorder with onset in infancy. Patients show global developmental delay, particularly of speech acquisition, as well as walking difficulties due to hypotonia, hypertonia, spasticity, or poor coordination. Other features include seizures, mild dysmorphic features, and variable short stature. The pregnancies tend to be complicated by hyper- or hypotension (summary by Ganapathi et al., 2019).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1672912">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1674629"><div><strong>Congenital hypotonia, epilepsy, developmental delay, and digital anomalies</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1674629</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.">C5193125</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">ATN1-related neurodevelopmental disorder (ATN1-NDD) is characterized by developmental delay / intellectual disability. Other neurologic findings can include infantile hypotonia, brain malformations, epilepsy, cortical visual impairment, and hearing loss. Feeding difficulties, present in some individuals, may require gastrostomy support when severe; similarly, respiratory issues, present in some, may require respiratory support after the neonatal period. Distinctive facial features and hand and foot differences are common. Other variable findings can include cardiac malformations and congenital anomalies of the kidney and urinary tract (CAKUT). To date, 18 individuals with ATN1-NDD have been identified.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1674629">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1841154"><div><strong>Muscular dystrophy, limb-girdle, autosomal recessive 28</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1841154</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.">C5830518</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive limb-girdle muscular dystrophy-28 (LGMDR28) is characterized by progressive muscle weakness affecting the proximal and axial muscles of the upper and lower limbs. The age at onset is highly variable, usually in the first decade, although onset in the fourth decade has also been reported. The disorder can be rapidly progressive or show a slower course. Most patients have limited ambulation or become wheelchair-bound within a few decades, and respiratory insufficiency commonly occurs. Laboratory studies show increased serum creatine kinase and elevated fasting blood glucose levels, although cholesterol is normal. EMG shows a myopathic pattern; muscle biopsy is generally unremarkable, but can show nonspecific myopathic or dystrophic features (Yogev et al., 2023; Morales-Rosado et al., 2023). For a discussion of genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy, see LGMDR1 (253600).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1841154">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_903483" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acrofacial dysostosis Cincinnati type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1674629" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital hypotonia, epilepsy, developmental delay, and digital anomalies</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1623077" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Facial palsy, congenital, with ptosis and velopharyngeal dysfunction</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_481914" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, autosomal dominant 10</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1841154" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Muscular dystrophy, limb-girdle, autosomal recessive 28</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1672912" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with seizures and speech and walking impairment</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934745" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">TELO2-related intellectual disability-neurodevelopmental disorder</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/37543906">Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ehtesham N,
|
||
Mosallaei M,
|
||
Beheshtian M,
|
||
Khoshbakht S,
|
||
Fadaee M,
|
||
Vazehan R,
|
||
Faraji Zonooz M,
|
||
Karimzadeh P,
|
||
Kahrizi K,
|
||
Najmabadi H</span><br />
|
||
<span class="medgenPMjournal">Arch Iran Med</span>
|
||
2022 Dec 1;25(12):788-797.
|
||
doi: 10.34172/aim.2022.124.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37543906" target="_blank">37543906</a><a href="/pmc/articles/PMC10685845" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25901057">Evidence-based guideline: Management of an unprovoked first seizure in adults: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the American Epilepsy Society.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krumholz A,
|
||
Wiebe S,
|
||
Gronseth GS,
|
||
Gloss DS,
|
||
Sanchez AM,
|
||
Kabir AA,
|
||
Liferidge AT,
|
||
Martello JP,
|
||
Kanner AM,
|
||
Shinnar S,
|
||
Hopp JL,
|
||
French JA</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2015 Apr 21;84(16):1705-13.
|
||
doi: 10.1212/WNL.0000000000001487.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25901057" target="_blank">25901057</a><a href="/pmc/articles/PMC4409581" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22brain%20imaging%20abnormality%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 (2)</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/39899098">First Seizures, Acute Repetitive Seizures, and Status Epilepticus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vossler DG</span><br />
|
||
<span class="medgenPMjournal">Continuum (Minneap Minn)</span>
|
||
2025 Feb 1;31(1):95-124.
|
||
doi: 10.1212/CON.0000000000001530.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39899098" target="_blank">39899098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35202928">Diagnostic delay in focal epilepsy: Association with brain pathology and age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yang M,
|
||
Tan KM,
|
||
Carney P,
|
||
Kwan P,
|
||
O'Brien TJ,
|
||
Berkovic SF,
|
||
Perucca P,
|
||
McIntosh AM</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2022 Mar;96:121-127.
|
||
Epub 2022 Feb 11
|
||
doi: 10.1016/j.seizure.2022.02.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35202928" target="_blank">35202928</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26844729">Management of a First Seizure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bergey GK</span><br />
|
||
<span class="medgenPMjournal">Continuum (Minneap Minn)</span>
|
||
2016 Feb;22(1 Epilepsy):38-50.
|
||
doi: 10.1212/CON.0000000000000271.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26844729" target="_blank">26844729</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25901057">Evidence-based guideline: Management of an unprovoked first seizure in adults: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the American Epilepsy Society.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krumholz A,
|
||
Wiebe S,
|
||
Gronseth GS,
|
||
Gloss DS,
|
||
Sanchez AM,
|
||
Kabir AA,
|
||
Liferidge AT,
|
||
Martello JP,
|
||
Kanner AM,
|
||
Shinnar S,
|
||
Hopp JL,
|
||
French JA</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2015 Apr 21;84(16):1705-13.
|
||
doi: 10.1212/WNL.0000000000001487.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25901057" target="_blank">25901057</a><a href="/pmc/articles/PMC4409581" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23499199">Recurrent hypersomnia following traumatic brain injury.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Billiard M,
|
||
Podesta C</span><br />
|
||
<span class="medgenPMjournal">Sleep Med</span>
|
||
2013 May;14(5):462-5.
|
||
Epub 2013 Mar 13
|
||
doi: 10.1016/j.sleep.2013.01.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23499199" target="_blank">23499199</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Brain%20imaging%20abnormality%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 (11)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39899098">First Seizures, Acute Repetitive Seizures, and Status Epilepticus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vossler DG</span><br />
|
||
<span class="medgenPMjournal">Continuum (Minneap Minn)</span>
|
||
2025 Feb 1;31(1):95-124.
|
||
doi: 10.1212/CON.0000000000001530.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39899098" target="_blank">39899098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35202928">Diagnostic delay in focal epilepsy: Association with brain pathology and age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yang M,
|
||
Tan KM,
|
||
Carney P,
|
||
Kwan P,
|
||
O'Brien TJ,
|
||
Berkovic SF,
|
||
Perucca P,
|
||
McIntosh AM</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2022 Mar;96:121-127.
|
||
Epub 2022 Feb 11
|
||
doi: 10.1016/j.seizure.2022.02.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35202928" target="_blank">35202928</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31337523">Detailed clinical course of fatal acute encephalopathy in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tomioka K,
|
||
Nishiyama M,
|
||
Nagase H,
|
||
Ishida Y,
|
||
Tanaka T,
|
||
Tokumoto S,
|
||
Yamaguchi H,
|
||
Toyoshima D,
|
||
Maruyama A,
|
||
Fujita K,
|
||
Aoki K,
|
||
Seino Y,
|
||
Nozu K,
|
||
Nishimura N,
|
||
Kurosawa H,
|
||
Iijima K</span><br />
|
||
<span class="medgenPMjournal">Brain Dev</span>
|
||
2019 Sep;41(8):691-698.
|
||
Epub 2019 Jul 20
|
||
doi: 10.1016/j.braindev.2019.04.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31337523" target="_blank">31337523</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26844729">Management of a First Seizure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bergey GK</span><br />
|
||
<span class="medgenPMjournal">Continuum (Minneap Minn)</span>
|
||
2016 Feb;22(1 Epilepsy):38-50.
|
||
doi: 10.1212/CON.0000000000000271.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26844729" target="_blank">26844729</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23499199">Recurrent hypersomnia following traumatic brain injury.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Billiard M,
|
||
Podesta C</span><br />
|
||
<span class="medgenPMjournal">Sleep Med</span>
|
||
2013 May;14(5):462-5.
|
||
Epub 2013 Mar 13
|
||
doi: 10.1016/j.sleep.2013.01.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23499199" target="_blank">23499199</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Brain%20imaging%20abnormality%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 (7)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39899098">First Seizures, Acute Repetitive Seizures, and Status Epilepticus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vossler DG</span><br />
|
||
<span class="medgenPMjournal">Continuum (Minneap Minn)</span>
|
||
2025 Feb 1;31(1):95-124.
|
||
doi: 10.1212/CON.0000000000001530.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39899098" target="_blank">39899098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31119857">Taking metformin and cognitive function change in older patients with diabetes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Koo BK,
|
||
Kim LK,
|
||
Lee JY,
|
||
Moon MK</span><br />
|
||
<span class="medgenPMjournal">Geriatr Gerontol Int</span>
|
||
2019 Aug;19(8):755-761.
|
||
Epub 2019 May 22
|
||
doi: 10.1111/ggi.13692.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31119857" target="_blank">31119857</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26844729">Management of a First Seizure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bergey GK</span><br />
|
||
<span class="medgenPMjournal">Continuum (Minneap Minn)</span>
|
||
2016 Feb;22(1 Epilepsy):38-50.
|
||
doi: 10.1212/CON.0000000000000271.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26844729" target="_blank">26844729</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25901057">Evidence-based guideline: Management of an unprovoked first seizure in adults: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the American Epilepsy Society.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krumholz A,
|
||
Wiebe S,
|
||
Gronseth GS,
|
||
Gloss DS,
|
||
Sanchez AM,
|
||
Kabir AA,
|
||
Liferidge AT,
|
||
Martello JP,
|
||
Kanner AM,
|
||
Shinnar S,
|
||
Hopp JL,
|
||
French JA</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2015 Apr 21;84(16):1705-13.
|
||
doi: 10.1212/WNL.0000000000001487.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25901057" target="_blank">25901057</a><a href="/pmc/articles/PMC4409581" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Brain%20imaging%20abnormality%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 (4)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31337523">Detailed clinical course of fatal acute encephalopathy in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tomioka K,
|
||
Nishiyama M,
|
||
Nagase H,
|
||
Ishida Y,
|
||
Tanaka T,
|
||
Tokumoto S,
|
||
Yamaguchi H,
|
||
Toyoshima D,
|
||
Maruyama A,
|
||
Fujita K,
|
||
Aoki K,
|
||
Seino Y,
|
||
Nozu K,
|
||
Nishimura N,
|
||
Kurosawa H,
|
||
Iijima K</span><br />
|
||
<span class="medgenPMjournal">Brain Dev</span>
|
||
2019 Sep;41(8):691-698.
|
||
Epub 2019 Jul 20
|
||
doi: 10.1016/j.braindev.2019.04.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31337523" target="_blank">31337523</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25901057">Evidence-based guideline: Management of an unprovoked first seizure in adults: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the American Epilepsy Society.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krumholz A,
|
||
Wiebe S,
|
||
Gronseth GS,
|
||
Gloss DS,
|
||
Sanchez AM,
|
||
Kabir AA,
|
||
Liferidge AT,
|
||
Martello JP,
|
||
Kanner AM,
|
||
Shinnar S,
|
||
Hopp JL,
|
||
French JA</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2015 Apr 21;84(16):1705-13.
|
||
doi: 10.1212/WNL.0000000000001487.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25901057" target="_blank">25901057</a><a href="/pmc/articles/PMC4409581" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19564586">Brain lesions are most often reversible in acute thrombotic thrombocytopenic purpura.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Burrus TM,
|
||
Wijdicks EF,
|
||
Rabinstein AA</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2009 Jul 7;73(1):66-70.
|
||
doi: 10.1212/WNL.0b013e3181aaea1b.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19564586" target="_blank">19564586</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18045694">Two-year prospective study of major depressive disorder in HIV-infected men.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Atkinson JH,
|
||
Heaton RK,
|
||
Patterson TL,
|
||
Wolfson T,
|
||
Deutsch R,
|
||
Brown SJ,
|
||
Summers J,
|
||
Sciolla A,
|
||
Gutierrez R,
|
||
Ellis RJ,
|
||
Abramson I,
|
||
Hesselink JR,
|
||
McCutchan JA,
|
||
Grant I;
|
||
HNRC Group</span><br />
|
||
<span class="medgenPMjournal">J Affect Disord</span>
|
||
2008 Jun;108(3):225-34.
|
||
Epub 2007 Nov 28
|
||
doi: 10.1016/j.jad.2007.10.017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18045694" target="_blank">18045694</a><a href="/pmc/articles/PMC2494949" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Brain%20imaging%20abnormality%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 (4)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31119857">Taking metformin and cognitive function change in older patients with diabetes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Koo BK,
|
||
Kim LK,
|
||
Lee JY,
|
||
Moon MK</span><br />
|
||
<span class="medgenPMjournal">Geriatr Gerontol Int</span>
|
||
2019 Aug;19(8):755-761.
|
||
Epub 2019 May 22
|
||
doi: 10.1111/ggi.13692.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31119857" target="_blank">31119857</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19564586">Brain lesions are most often reversible in acute thrombotic thrombocytopenic purpura.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Burrus TM,
|
||
Wijdicks EF,
|
||
Rabinstein AA</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2009 Jul 7;73(1):66-70.
|
||
doi: 10.1212/WNL.0b013e3181aaea1b.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19564586" target="_blank">19564586</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18045694">Two-year prospective study of major depressive disorder in HIV-infected men.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Atkinson JH,
|
||
Heaton RK,
|
||
Patterson TL,
|
||
Wolfson T,
|
||
Deutsch R,
|
||
Brown SJ,
|
||
Summers J,
|
||
Sciolla A,
|
||
Gutierrez R,
|
||
Ellis RJ,
|
||
Abramson I,
|
||
Hesselink JR,
|
||
McCutchan JA,
|
||
Grant I;
|
||
HNRC Group</span><br />
|
||
<span class="medgenPMjournal">J Affect Disord</span>
|
||
2008 Jun;108(3):225-34.
|
||
Epub 2007 Nov 28
|
||
doi: 10.1016/j.jad.2007.10.017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18045694" target="_blank">18045694</a><a href="/pmc/articles/PMC2494949" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Brain%20imaging%20abnormality%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 (3)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
||
|
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|
||
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|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
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|
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|
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Brain%20imaging%20abnormality" 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=(%22brain%20imaging%20abnormality%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><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Brain%20imaging%20abnormality%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. 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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<a href="/pubmed?term=Brain%20imaging%20abnormality%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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