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<meta name="keywords" content="C3806403, continuous spike and waves during slow sleep, continuous spikes and waves during sleep, continuous spikes and waves during slow-wave sleep, csws, cswss syndrome, electrical status epilepticus during slow-wave sleep, epileptic encephalopathy with continuous spike-and-wave during slow sleep, finding, 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="Diffuse, bilateral and recently also unilateral or focal localization spike-wave occurring in slow sleep or non-rapid eye movement sleep." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=812733
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ConceptID=C3806403
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Continuous spike and waves during slow sleep</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>812733</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:">C3806403</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Continuous spikes and waves during sleep; Continuous spikes and waves during slow-wave sleep; CSWS; CSWSS syndrome; Electrical status epilepticus during slow-wave sleep; Epileptic encephalopathy with continuous spike-and-wave during slow sleep</td></tr>
|
||
<tr><td>Modes of inheritance:</td>
|
||
<td>
|
||
<div class="divPopper rprt" id="moi_141047"><div><strong>Autosomal dominant inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141047</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.">C0443147</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Intellectual Product</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.</div></div>
|
||
<div class="divPopper rprt" id="moi_988794"><div><strong>Not genetically inherited</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>988794</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier assigned by MedGen (starting with CN) for terms that cannot be identified in NLM's Unified Medical Language system (UMLS) Click for more information.">CN307044</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">clinical entity without genetic inheritance.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/988794">This record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_141047" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant inheritance</a><span> (Orphanet)</span></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_988794" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Not genetically inherited</a><span> (Orphanet)</span></div></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:0031491">HP:0031491</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=725">ORPHA725</a></td></tr></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>
|
||
<div class="portlet mgSection" id="ID_100">
|
||
<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">Diffuse, bilateral and recently also unilateral or focal localization spike-wave occurring in slow sleep or non-rapid eye movement sleep. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_118">
|
||
<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">Continuous spike and waves during slow sleep</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/1843031" ref="tree=MeSH" title="MedGen record for Childhood-onset epilepsy syndrome">Childhood-onset epilepsy syndrome</a></span><ul><li><span class="matched_ds">Continuous spike and waves during slow sleep</span></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<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_79465"><div><strong>Landau-Kleffner syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>79465</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.">C0282512</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">GRIN2A-related disorders encompass a broad phenotypic spectrum that includes developmental delay evolving to intellectual disability (DD/ID), epilepsy, speech and language disorders, movement disorders, and neuropsychiatric disorders. Intellect ranges from normal to profoundly impaired. Observed speech disorders include dysarthria and speech dyspraxia, and both receptive and expressive language delays; more mildly affected individuals may display subtly impaired intelligibility of conversational speech. Epilepsy features include seizure onset usually between ages three and six years, focal epilepsy with language and/or global developmental regression, and electroencephalogram (EEG) abnormalities, including continuous spike-and-wave discharges in sleep or very active centrotemporal discharges. Epilepsy is typically focal and ranges from self-limited epilepsy with centrotemporal spikes to developmental and/or epileptic encephalopathies (DEE/EE), including the syndromes of DEE/EE with spike-wave activation in sleep (DEE/EE-SWAS), which include Landau-Kleffner syndrome. Movement disorders occur less frequently and include ataxia, dystonia, and chorea.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/79465">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_350085"><div><strong>Spinocerebellar ataxia type 29</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>350085</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.">C1861732</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spinocerebellar ataxia-29 (SCA29) is an autosomal dominant neurologic disorder characterized by onset in infancy of delayed motor development and mild cognitive delay. Affected individuals develop a very slowly progressive or nonprogressive gait and limb ataxia associated with cerebellar atrophy on brain imaging. Additional variable features include nystagmus, dysarthria, and tremor (summary by Huang et al., 2012). For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/350085">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1624740"><div><strong>Intellectual disability, X-linked, syndromic, Houge type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1624740</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.">C4538788</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The Houge type of X-linked syndromic intellectual developmental disorder (MRXSHG) is characterized by delayed development, intellectual disability, speech and language delay, and early-onset seizures. EEG tends to show continuous spike-wave activity or centrotemporal spikes. Some patients may have remission of seizures by adolescence. Carrier females may be mildly affected (summary by Damiano et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1624740">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794148"><div><strong>Focal segmental glomerulosclerosis and neurodevelopmental syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794148</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.">C5561938</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Focal segmental glomerulosclerosis and neurodevelopmental syndrome (FSGSNEDS) is characterized by global developmental delay and renal dysfunction manifest as proteinuria and nephrotic syndrome apparent from infancy or early childhood. Some patients present with renal disease, whereas others present with developmental delay and develop renal disease later in childhood. Renal biopsy shows focal segmental glomerulosclerosis (FSGS), but the course of the disease is variable: some patients have transient proteinuria and others require renal transplant. Neurodevelopmental features are also variable, with some patients having only mildly impaired intellectual development, and others having a severe developmental disorder associated with early-onset refractory seizures or epileptic encephalopathy. Additional features, including feeding difficulties, poor overall growth, and nonspecific dysmorphic facial features, are commonly observed (summary by Assoum et al., 2018 and Weng et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794148">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1809962"><div><strong>Developmental and epileptic encephalopathy 103</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1809962</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.">C5677002</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Developmental and epileptic encephalopathy-103 (DEE103) is characterized by onset of various types of seizures in the first year of life, most of which are refractory to treatment. Affected individuals show global developmental delay with impaired intellectual development ranging from mild to severe. Additional features may include hypotonia, ataxia, and behavioral abnormalities, including autism and hyperactivity (Schwarz et al., 2022). For a general phenotypic description and a discussion of genetic heterogeneity of DEE, see 308350.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1809962">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1824038"><div><strong>Developmental and epileptic encephalopathy 110</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1824038</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.">C5774265</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Developmental and epileptic encephalopathy-110 (DEE110) is an autosomal recessive disorder characterized by profound global developmental delay and hypotonia apparent in infancy followed by onset of seizures in the first months or years of life. Affected individuals achieve almost no developmental milestones and show impaired intellectual development, poor or absent speech, inability to walk or grasp objects, peripheral spasticity, and poor eye contact. Brain imaging shows hypoplastic corpus callosum and cortical atrophy (Dahimene et al., 2022). For a discussion of genetic heterogeneity of DEE, see 308350.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1824038">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1840880"><div><strong>Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1840880</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.">C5830244</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">TRPM3-related neurodevelopmental disorder (TRPM3-NDD) is characterized by congenital hypotonia, developmental delay affecting motor and speech/language skills, mild-to-severe intellectual disability, seizures, ophthalmologic manifestations including strabismus, nystagmus, and refractive errors, and musculoskeletal manifestations (e.g., talipes equinovarus, hip dysplasia, scoliosis). Reported seizure types include febrile, absence, generalized tonic-clonic, infantile spasms, and atonic drops. Cerebellar atrophy may be seen on brain MRI.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1840880">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1809962" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental and epileptic encephalopathy 103</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1824038" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental and epileptic encephalopathy 110</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794148" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Focal segmental glomerulosclerosis and neurodevelopmental syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1624740" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, X-linked, syndromic, Houge type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_79465" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Landau-Kleffner syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1840880" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_350085" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 29</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/1985831">Epilepsy with continuous spike-waves during slow sleep and its treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yasuhara A,
|
||
Yoshida H,
|
||
Hatanaka T,
|
||
Sugimoto T,
|
||
Kobayashi Y,
|
||
Dyken E</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
1991 Jan-Feb;32(1):59-62.
|
||
doi: 10.1111/j.1528-1157.1991.tb05612.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1985831" target="_blank">1985831</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22continuous%20spike%20and%20waves%20during%20slow%20sleep%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 (1)</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/35063695">Panayiotopoulos syndrome: Unusual clinical manifestations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Semprino M,
|
||
Galicchio S,
|
||
Espeche A,
|
||
Cersosimo R,
|
||
Chacon S,
|
||
Gamboni B,
|
||
Adi J,
|
||
Fasulo L,
|
||
Fortini S,
|
||
Cachia P,
|
||
Gallo A,
|
||
Caraballo RH</span><br />
|
||
<span class="medgenPMjournal">Epilepsy Behav</span>
|
||
2022 Mar;128:108552.
|
||
Epub 2022 Jan 18
|
||
doi: 10.1016/j.yebeh.2022.108552.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35063695" target="_blank">35063695</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31262717">Encephalopathy with continuous spike-waves during slow-wave sleep: evolution and prognosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Caraballo R,
|
||
Pavlidis E,
|
||
Nikanorova M,
|
||
Loddenkemper T</span><br />
|
||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2019 Jun 1;21(S1):15-21.
|
||
doi: 10.1684/epd.2019.1052.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31262717" target="_blank">31262717</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29168169">Response to clobazam in continuous spike-wave during sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vega C,
|
||
Sánchez Fernández I,
|
||
Peters J,
|
||
Thome-Souza MS,
|
||
Jackson M,
|
||
Takeoka M,
|
||
Wilkening GN,
|
||
Pearl PL,
|
||
Chapman K,
|
||
Loddenkemper T</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2018 Mar;60(3):283-289.
|
||
Epub 2017 Nov 23
|
||
doi: 10.1111/dmcn.13607.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29168169" target="_blank">29168169</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21399511">Continuous spike and waves during sleep and electrical status epilepticus in sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Loddenkemper T,
|
||
Fernández IS,
|
||
Peters JM</span><br />
|
||
<span class="medgenPMjournal">J Clin Neurophysiol</span>
|
||
2011 Apr;28(2):154-64.
|
||
doi: 10.1097/WNP.0b013e31821213eb.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21399511" target="_blank">21399511</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2187021">Unusual EEG patterns.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Westmoreland BF,
|
||
Klass DW</span><br />
|
||
<span class="medgenPMjournal">J Clin Neurophysiol</span>
|
||
1990 Apr;7(2):209-28.
|
||
doi: 10.1097/00004691-199004000-00005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2187021" target="_blank">2187021</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Continuous%20spike%20and%20waves%20during%20slow%20sleep%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 (79)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35489823">Long-term outcome of developmental and epileptic encephalopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Van Bogaert P</span><br />
|
||
<span class="medgenPMjournal">Rev Neurol (Paris)</span>
|
||
2022 Sep;178(7):659-665.
|
||
Epub 2022 Apr 27
|
||
doi: 10.1016/j.neurol.2022.01.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35489823" target="_blank">35489823</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31262717">Encephalopathy with continuous spike-waves during slow-wave sleep: evolution and prognosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Caraballo R,
|
||
Pavlidis E,
|
||
Nikanorova M,
|
||
Loddenkemper T</span><br />
|
||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2019 Jun 1;21(S1):15-21.
|
||
doi: 10.1684/epd.2019.1052.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31262717" target="_blank">31262717</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21399511">Continuous spike and waves during sleep and electrical status epilepticus in sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Loddenkemper T,
|
||
Fernández IS,
|
||
Peters JM</span><br />
|
||
<span class="medgenPMjournal">J Clin Neurophysiol</span>
|
||
2011 Apr;28(2):154-64.
|
||
doi: 10.1097/WNP.0b013e31821213eb.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21399511" target="_blank">21399511</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20598941">Epilepsy with continuous spikes and waves during slow wave sleep in a child diagnosed with pervasive developmental disorder-not otherwise specified.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Neiman ES,
|
||
Seyffert M,
|
||
Richards A,
|
||
Gupta D,
|
||
Chokroverty S</span><br />
|
||
<span class="medgenPMjournal">Sleep Med</span>
|
||
2010 Sep;11(8):799-802.
|
||
Epub 2010 Jul 3
|
||
doi: 10.1016/j.sleep.2010.04.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20598941" target="_blank">20598941</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11520318">Epileptic encephalopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dulac O</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2001;42 Suppl 3:23-6.
|
||
doi: 10.1046/j.1528-1157.2001.042suppl.3023.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11520318" target="_blank">11520318</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Continuous%20spike%20and%20waves%20during%20slow%20sleep%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 (103)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34750092">Continuous spikes and waves during slow sleep related to sulthiame?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Caraballo RH,
|
||
Galicchio S</span><br />
|
||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2022 Feb 1;24(1):208-210.
|
||
doi: 10.1684/epd.2021.1359.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34750092" target="_blank">34750092</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29168169">Response to clobazam in continuous spike-wave during sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vega C,
|
||
Sánchez Fernández I,
|
||
Peters J,
|
||
Thome-Souza MS,
|
||
Jackson M,
|
||
Takeoka M,
|
||
Wilkening GN,
|
||
Pearl PL,
|
||
Chapman K,
|
||
Loddenkemper T</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2018 Mar;60(3):283-289.
|
||
Epub 2017 Nov 23
|
||
doi: 10.1111/dmcn.13607.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29168169" target="_blank">29168169</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23666433">Epileptic encephalopathy with continuous spikes and waves during sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Striano P,
|
||
Capovilla G</span><br />
|
||
<span class="medgenPMjournal">Curr Neurol Neurosci Rep</span>
|
||
2013 Jul;13(7):360.
|
||
doi: 10.1007/s11910-013-0360-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23666433" target="_blank">23666433</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20727484">Nonconvulsive status epilepticus and continuous spike and slow wave of sleep in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Akman CI</span><br />
|
||
<span class="medgenPMjournal">Semin Pediatr Neurol</span>
|
||
2010 Sep;17(3):155-62.
|
||
doi: 10.1016/j.spen.2010.06.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20727484" target="_blank">20727484</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11520318">Epileptic encephalopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dulac O</span><br />
|
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<span class="medgenPMjournal">Epilepsia</span>
|
||
2001;42 Suppl 3:23-6.
|
||
doi: 10.1046/j.1528-1157.2001.042suppl.3023.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11520318" target="_blank">11520318</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Continuous%20spike%20and%20waves%20during%20slow%20sleep%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 (56)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31262717">Encephalopathy with continuous spike-waves during slow-wave sleep: evolution and prognosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Caraballo R,
|
||
Pavlidis E,
|
||
Nikanorova M,
|
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Loddenkemper T</span><br />
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||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2019 Jun 1;21(S1):15-21.
|
||
doi: 10.1684/epd.2019.1052.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31262717" target="_blank">31262717</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29168169">Response to clobazam in continuous spike-wave during sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vega C,
|
||
Sánchez Fernández I,
|
||
Peters J,
|
||
Thome-Souza MS,
|
||
Jackson M,
|
||
Takeoka M,
|
||
Wilkening GN,
|
||
Pearl PL,
|
||
Chapman K,
|
||
Loddenkemper T</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2018 Mar;60(3):283-289.
|
||
Epub 2017 Nov 23
|
||
doi: 10.1111/dmcn.13607.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29168169" target="_blank">29168169</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23666433">Epileptic encephalopathy with continuous spikes and waves during sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Striano P,
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Capovilla G</span><br />
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<span class="medgenPMjournal">Curr Neurol Neurosci Rep</span>
|
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2013 Jul;13(7):360.
|
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doi: 10.1007/s11910-013-0360-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23666433" target="_blank">23666433</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21399511">Continuous spike and waves during sleep and electrical status epilepticus in sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Loddenkemper T,
|
||
Fernández IS,
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Peters JM</span><br />
|
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<span class="medgenPMjournal">J Clin Neurophysiol</span>
|
||
2011 Apr;28(2):154-64.
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doi: 10.1097/WNP.0b013e31821213eb.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21399511" target="_blank">21399511</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20727484">Nonconvulsive status epilepticus and continuous spike and slow wave of sleep in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Akman CI</span><br />
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||
<span class="medgenPMjournal">Semin Pediatr Neurol</span>
|
||
2010 Sep;17(3):155-62.
|
||
doi: 10.1016/j.spen.2010.06.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20727484" target="_blank">20727484</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Continuous%20spike%20and%20waves%20during%20slow%20sleep%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 (75)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31262717">Encephalopathy with continuous spike-waves during slow-wave sleep: evolution and prognosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Caraballo R,
|
||
Pavlidis E,
|
||
Nikanorova M,
|
||
Loddenkemper T</span><br />
|
||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2019 Jun 1;21(S1):15-21.
|
||
doi: 10.1684/epd.2019.1052.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31262717" target="_blank">31262717</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29168169">Response to clobazam in continuous spike-wave during sleep.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vega C,
|
||
Sánchez Fernández I,
|
||
Peters J,
|
||
Thome-Souza MS,
|
||
Jackson M,
|
||
Takeoka M,
|
||
Wilkening GN,
|
||
Pearl PL,
|
||
Chapman K,
|
||
Loddenkemper T</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2018 Mar;60(3):283-289.
|
||
Epub 2017 Nov 23
|
||
doi: 10.1111/dmcn.13607.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29168169" target="_blank">29168169</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27435520">Idiopathic focal epilepsies: the "lost tribe".</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pal DK,
|
||
Ferrie C,
|
||
Addis L,
|
||
Akiyama T,
|
||
Capovilla G,
|
||
Caraballo R,
|
||
de Saint-Martin A,
|
||
Fejerman N,
|
||
Guerrini R,
|
||
Hamandi K,
|
||
Helbig I,
|
||
Ioannides AA,
|
||
Kobayashi K,
|
||
Lal D,
|
||
Lesca G,
|
||
Muhle H,
|
||
Neubauer BA,
|
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Pisano T,
|
||
Rudolf G,
|
||
Seegmuller C,
|
||
Shibata T,
|
||
Smith A,
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||
Striano P,
|
||
Strug LJ,
|
||
Szepetowski P,
|
||
Valeta T,
|
||
Yoshinaga H,
|
||
Koutroumanidis M</span><br />
|
||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2016 Sep 1;18(3):252-88.
|
||
doi: 10.1684/epd.2016.0839.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27435520" target="_blank">27435520</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25965811">Sleep and epilepsy syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schmitt B</span><br />
|
||
<span class="medgenPMjournal">Neuropediatrics</span>
|
||
2015 Jun;46(3):171-80.
|
||
Epub 2015 May 12
|
||
doi: 10.1055/s-0035-1551574.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25965811" target="_blank">25965811</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10996552">Spike-and-wave discharges of absence seizures as a transformation of sleep spindles: the continuing development of a hypothesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kostopoulos GK</span><br />
|
||
<span class="medgenPMjournal">Clin Neurophysiol</span>
|
||
2000 Sep;111 Suppl 2:S27-38.
|
||
doi: 10.1016/s1388-2457(00)00399-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10996552" target="_blank">10996552</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Continuous%20spike%20and%20waves%20during%20slow%20sleep%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 (44)</a></div></div>
|
||
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|
||
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|
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|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67cec1dd84f3725e59acceb2">Continuous spike and waves during slow sleep</a>
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