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<meta name="keywords" content="C5562017, atp1a2, dee98, developmental and epileptic encephalopathy 98, disease or syndrome, 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="Developmental and epileptic encephalopathy-98 (DEE98) is characterized by onset of seizures in the first decade (range infancy to late childhood) associated with variable global developmental delay. Other features may include hypotonia, spasticity, and quadriparesis. Brain imaging may be normal or show nonspecific and variable abnormalities, including polymicrogyria. The severity is variable; some patients may die of refractory status epilepticus (summary by Vetro et al., 2021).&#13; For a general phenotypic description and a discussion of genetic heterogeneity of DEE, see 308350." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Developmental and epileptic encephalopathy 98 (Concept Id: C5562017)
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<!--
UID=1794227
ConceptID=C5562017
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Developmental and epileptic encephalopathy 98<span class="h1sub">(DEE98)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794227</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)&#10;Click for more information."><span class="highlight" style="background-color:">C5562017</span></a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
<td>DEE98; DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 98</td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Gene (location):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
Gene(s) directly associated with<br />
this condition or phenotype.</div></td>
<td><a target="_blank" title="ATP1A2 - ID: 477 - NCBI Gene" href="/gene/477" class="medgenPMinfo">ATP1A2</a> (1q23.2)</td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
<td><a href="https://monarchinitiative.org/disease/MONDO:0030472" target="_blank">MONDO:0030472</a></td></tr>
<tr><td>OMIM<span class="superscript">®</span>:</td>
<td><a href="https://omim.org/entry/619605" target="_blank">619605</a></td></tr>
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<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">Developmental and epileptic encephalopathy-98 (DEE98) is characterized by onset of seizures in the first decade (range infancy to late childhood) associated with variable global developmental delay. Other features may include hypotonia, spasticity, and quadriparesis. Brain imaging may be normal or show nonspecific and variable abnormalities, including polymicrogyria. The severity is variable; some patients may die of refractory status epilepticus (summary by Vetro et al., 2021).&#13; For a general phenotypic description and a discussion of genetic heterogeneity of DEE, see 308350. [from <a title="Online Mendelian Inheritance in Man" href="http://www.omim.org" class="defSource" target="_blank">OMIM</a>]</div>
</div>
<div class="portlet mgSection" id="ID_102">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
<div class="divPopper rprt" id="clin_11458"><div><strong>Sleep apnea</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>11458</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)&#10;Click for more information.">C0037315</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">An intermittent cessation of airflow at the mouth and nose during sleep is known as sleep apnea. Apneas that last at least 10 seconds are considered significant, but individuals with sleep apnea may experience apneas lasting from 20 seconds up to 2 or 3 minutes. Patients may have up to 15 events per hour of sleep.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/11458">Feature record</a> | <a href="/medgen?term=%22Sleep%20apnea%22%5BClinical%20Features%5D%20OR%2011458%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_66708"><div><strong>Clonic seizure</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>66708</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)&#10;Click for more information.">C0234535</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">A clonic seizure is a type of motor seizure characterized by sustained rhythmic jerking, that is regularly repetitive.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/66708">Feature record</a> | <a href="/medgen?term=%22Clonic%20seizure%22%5BClinical%20Features%5D%20OR%2066708%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_116012"><div><strong>Cerebral atrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>116012</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)&#10;Click for more information.">C0235946</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Atrophy (wasting, decrease in size of cells or tissue) affecting the cerebrum.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/116012">Feature record</a> | <a href="/medgen?term=%22Cerebral%20atrophy%22%5BClinical%20Features%5D%20OR%20116012%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_141670"><div><strong>Bilateral tonic-clonic seizure</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141670</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)&#10;Click for more information.">C0494475</a></dd><dt><span class="dotprefix"></span></dt><dd>Sign or Symptom</dd></dl></div></div></div>
<div class="spaceAbove">A bilateral tonic-clonic seizure is a seizure defined by a tonic (bilateral increased tone, lasting seconds to minutes) and then a clonic (bilateral sustained rhythmic jerking) phase.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/141670">Feature record</a> | <a href="/medgen?term=%22Bilateral%20tonic-clonic%20seizure%22%5BClinical%20Features%5D%20OR%20141670%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_107838"><div><strong>Global developmental delay</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>107838</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)&#10;Click for more information.">C0557874</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">A delay in the achievement of motor or mental milestones in the domains of development of a child, including motor skills, speech and language, cognitive skills, and social and emotional skills. This term should only be used to describe children younger than five years of age.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/107838">Feature record</a> | <a href="/medgen?term=%22Global%20developmental%20delay%22%5BClinical%20Features%5D%20OR%20107838%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_196624"><div><strong>Cerebellar atrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>196624</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)&#10;Click for more information.">C0740279</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Cerebellar atrophy is defined as a cerebellum with initially normal structures, in a posterior fossa with normal size, which displays enlarged fissures (interfolial spaces) in comparison to the foliae secondary to loss of tissue. Cerebellar atrophy implies irreversible loss of tissue and result from an ongoing progressive disease until a final stage is reached or a single injury, e.g. an intoxication or infectious event.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/196624">Feature record</a> | <a href="/medgen?term=%22Cerebellar%20atrophy%22%5BClinical%20Features%5D%20OR%20196624%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_199670"><div><strong>Focal-onset seizure</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>199670</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)&#10;Click for more information.">C0751495</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">A focal-onset seizure is a type of seizure originating within networks limited to one hemisphere. They may be discretely localized or more widely distributed, and may originate in subcortical structures.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/199670">Feature record</a> | <a href="/medgen?term=%22Focal-onset%20seizure%22%5BClinical%20Features%5D%20OR%20199670%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_164077"><div><strong>Bilateral tonic-clonic seizure with focal onset</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>164077</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)&#10;Click for more information.">C0877017</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">A bilateral tonic-clonic seizure with focal onset is a focal-onset seizure which progresses into a bilateral tonic-clonic phase.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/164077">Feature record</a> | <a href="/medgen?term=%22Bilateral%20tonic-clonic%20seizure%20with%20focal%20onset%22%5BClinical%20Features%5D%20OR%20164077%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_220387"><div><strong>Attention deficit hyperactivity disorder</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>220387</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)&#10;Click for more information.">C1263846</a></dd><dt><span class="dotprefix"></span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
<div class="spaceAbove">Attention-deficit/hyperactivity disorder (ADHD) is a behavioral disorder that typically begins in childhood and is characterized by a short attention span (inattention), an inability to be calm and stay still (hyperactivity), and poor impulse control (impulsivity). Some people with ADHD have problems with only inattention or with hyperactivity and impulsivity, but most have problems related to all three features.\n\nIn people with ADHD, the characteristic behaviors are frequent and severe enough to interfere with the activities of daily living such as school, work, and relationships with others. Because of an inability to stay focused on tasks, people with inattention may be easily distracted, forgetful, avoid tasks that require sustained attention, have difficulty organizing tasks, or frequently lose items.\n\nHyperactivity is usually shown by frequent movement. Individuals with this feature often fidget or tap their foot when seated, leave their seat when it is inappropriate to do so (such as in the classroom), or talk a lot and interrupt others.\n\nImpulsivity can result in hasty actions without thought for the consequences. Individuals with poor impulse control may have difficulty waiting for their turn, deferring to others, or considering their actions before acting.\n\nMore than two-thirds of all individuals with ADHD have additional conditions, including insomnia, mood or anxiety disorders, learning disorders, or substance use disorders. Affected individuals may also have autism spectrum disorder, which is characterized by impaired communication and social interaction, or Tourette syndrome, which is a disorder characterized by repetitive and involuntary movements or noises called tics.\n\nIn most affected individuals, ADHD continues throughout life, but in about one-third of individuals, signs and symptoms of ADHD go away by adulthood.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/220387">Feature record</a> | <a href="/medgen?term=%22Attention%20deficit%20hyperactivity%20disorder%22%5BClinical%20Features%5D%20OR%20220387%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_303190"><div><strong>Reduced eye contact</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>303190</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)&#10;Click for more information.">C1445953</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">A reduced frequency or duration of eye contact.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/303190">Feature record</a> | <a href="/medgen?term=%22Reduced%20eye%20contact%22%5BClinical%20Features%5D%20OR%20303190%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_371993"><div><strong>Thick corpus callosum</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>371993</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)&#10;Click for more information.">C1835194</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">Increased vertical dimension of the corpus callosum. This feature can be visualized by sagittal sections on magnetic resonance tomography imaging of the brain.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/371993">Feature record</a> | <a href="/medgen?term=%22Thick%20corpus%20callosum%22%5BClinical%20Features%5D%20OR%20371993%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_340737"><div><strong>Absent speech</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>340737</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)&#10;Click for more information.">C1854882</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">Complete lack of development of speech and language abilities.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/340737">Feature record</a> | <a href="/medgen?term=%22Absent%20speech%22%5BClinical%20Features%5D%20OR%20340737%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_369943"><div><strong>EEG with burst suppression</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>369943</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)&#10;Click for more information.">C1969156</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">The burst suppression pattern in electroencephalography refers to a characteristic periodic pattern of low voltage (&lt;10 microvolts) suppressed background and a relatively shorter pattern of higher amplitude slow, sharp, and spiking complexes.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/369943">Feature record</a> | <a href="/medgen?term=%22EEG%20with%20burst%20suppression%22%5BClinical%20Features%5D%20OR%20369943%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_481305"><div><strong>Perisylvian polymicrogyria</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>481305</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)&#10;Click for more information.">C3279675</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">Polymicrogyria (an excessive number of small gyri or convolutions) that is maximal in perisylvian regions (the regions that surround the Sylvian fissures), which may be symmetric or asymmetric and may extend beyond perisylvian regions. The Sylvian fissures often extend posteriorly and superiorly.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/481305">Feature record</a> | <a href="/medgen?term=%22Perisylvian%20polymicrogyria%22%5BClinical%20Features%5D%20OR%20481305%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_1713873"><div><strong>Refractory status epilepticus</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1713873</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)&#10;Click for more information.">C5397872</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Refractory status epilepticus is defined as status epilepticus continuing despite two appropriately selected and dosed antiepileptic drugs, including a benzodiazepine.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1713873">Feature record</a> | <a href="/medgen?term=%22Refractory%20status%20epilepticus%22%5BClinical%20Features%5D%20OR%201713873%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_1785336"><div><strong>Thin corpus callosum</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1785336</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)&#10;Click for more information.">C5441562</a></dd><dt><span class="dotprefix"></span></dt><dd>Anatomical Abnormality</dd></dl></div></div></div>
<div class="spaceAbove">An abnormally thin corpus callous, due to atrophy, hypoplasia or agenesis. This term is intended to be used in situations where it is not known if thinning of the corpus callosum (for instance, as visualized by magnetic resonance tomography) is due to abnormal development (e.g. a leukodystrophy) or atrophy following normal development (e.g. neurodegeneration).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1785336">Feature record</a> | <a href="/medgen?term=%22Thin%20corpus%20callosum%22%5BClinical%20Features%5D%20OR%201785336%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_10133"><div><strong>Hypotonia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>10133</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)&#10;Click for more information.">C0026827</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">Hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle). Even when relaxed, muscles have a continuous and passive partial contraction which provides some resistance to passive stretching. Hypotonia thus manifests as diminished resistance to passive stretching. Hypotonia is not the same as muscle weakness, although the two conditions can co-exist.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/10133">Feature record</a> | <a href="/medgen?term=%22Hypotonia%22%5BClinical%20Features%5D%20OR%2010133%5Buid%5D">Search on this feature</a></div></div>
<div class="divPopper rprt" id="clin_608952"><div><strong>Secondary microcephaly</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>608952</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)&#10;Click for more information.">C0431352</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">Head circumference which falls below 2 standard deviations below the mean for age and gender because of insufficient head growth after birth.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/608952">Feature record</a> | <a href="/medgen?term=%22Secondary%20microcephaly%22%5BClinical%20Features%5D%20OR%20608952%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite" data-jigconfig="closed: 1"><div class="concept-def"><a class="small" href="#" onclick="jQuery(&quot;.TreeLite&quot;,&quot;#ID_102&quot;).TreeLite().openAll(); return false;">Show all</a><a class="small" href="#" onclick="jQuery(&quot;.TreeLite&quot;,&quot;#ID_102&quot;).TreeLite().closeAll(); return false;">Hide all</a></div><ul><li><span class="TLline">Abnormality of the musculoskeletal system</span><ul><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_10133" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypotonia</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_608952" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Secondary microcephaly</a></span></li></ul></li><li><span class="TLline">Abnormality of the nervous system</span><ul><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_340737" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Absent speech</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_220387" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Attention deficit hyperactivity disorder</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_141670" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Bilateral tonic-clonic seizure</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_164077" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Bilateral tonic-clonic seizure with focal onset</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_196624" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebellar atrophy</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_116012" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebral atrophy</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_66708" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Clonic seizure</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_369943" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">EEG with burst suppression</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_199670" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Focal-onset seizure</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_107838" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Global developmental delay</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_481305" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Perisylvian polymicrogyria</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_303190" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Reduced eye contact</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_1713873" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Refractory status epilepticus</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_11458" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Sleep apnea</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_371993" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Thick corpus callosum</a></span></li><li class="TLline">
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_1785336" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Thin corpus callosum</a></span></li></ul></li></ul></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/33754312">Highly Purified Cannabidiol for Epilepsy Treatment: A Systematic Review of Epileptic Conditions Beyond Dravet Syndrome and Lennox-Gastaut Syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lattanzi S,
Trinka E,
Striano P,
Rocchi C,
Salvemini S,
Silvestrini M,
Brigo F</span><br />
<span class="medgenPMjournal">CNS Drugs</span>
2021 Mar;35(3):265-281.
Epub 2021 Mar 22
doi: 10.1007/s40263-021-00807-y.
<span class="bold">PMID: </span><a href="/pubmed/33754312" target="_blank">33754312</a><a href="/pmc/articles/PMC8005394" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29320603">Drug management for acute tonic-clonic convulsions including convulsive status epilepticus in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">McTague A,
Martland T,
Appleton R</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Jan 10;1(1):CD001905.
doi: 10.1002/14651858.CD001905.pub3.
<span class="bold">PMID: </span><a href="/pubmed/29320603" target="_blank">29320603</a><a href="/pmc/articles/PMC6491279" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25134878">Primary care for adults on the autism spectrum.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Nicolaidis C,
Kripke CC,
Raymaker D</span><br />
<span class="medgenPMjournal">Med Clin North Am</span>
2014 Sep;98(5):1169-91.
doi: 10.1016/j.mcna.2014.06.011.
<span class="bold">PMID: </span><a href="/pubmed/25134878" target="_blank">25134878</a><a href="/pmc/articles/PMC4851469" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(developmental%20and%20epileptic%20encephalopathy%2098)%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 (10)</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/38380699">L-serine treatment in patients with GRIN-related encephalopathy: a phase 2A, non-randomized study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Juliá-Palacios N,
Olivella M,
Sigatullina Bondarenko M,
Ibáñez-Micó S,
Muñoz-Cabello B,
Alonso-Luengo O,
Soto-Insuga V,
García-Navas D,
Cuesta-Herraiz L,
Andreo-Lillo P,
Aguilera-Albesa S,
Hedrera-Fernández A,
González Alguacil E,
Sánchez-Carpintero R,
Martín Del Valle F,
Jiménez González E,
Cean Cabrera L,
Medina-Rivera I,
Perez-Ordoñez M,
Colomé R,
Lopez L,
Engracia Cazorla M,
Fornaguera M,
Ormazabal A,
Alonso-Colmenero I,
Illescas KS,
Balsells-Mejía S,
Mari-Vico R,
Duffo Viñas M,
Cappuccio G,
Terrone G,
Romano R,
Manti F,
Mastrangelo M,
Alfonsi C,
de Siqueira Barros B,
Nizon M,
Gjerulfsen CE,
Muro VL,
Karall D,
Zeiner F,
Masnada S,
Peterlongo I,
Oyarzábal A,
Santos-Gómez A,
Altafaj X,
García-Cazorla Á</span><br />
<span class="medgenPMjournal">Brain</span>
2024 May 3;147(5):1653-1666.
doi: 10.1093/brain/awae041.
<span class="bold">PMID: </span><a href="/pubmed/38380699" target="_blank">38380699</a></div>
<div class="nl"><a target="_blank" href="/pubmed/38290094">Outcome of Epilepsy Surgery in MRI-Negative Patients Without Histopathologic Abnormalities in the Resected Tissue.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Sanders MW,
Van der Wolf I,
Jansen FE,
Aronica E,
Helmstaedter C,
Racz A,
Surges R,
Grote A,
Becker AJ,
Rheims S,
Catenoix H,
Duncan JS,
De Tisi J,
Jacques TS,
Cross JH,
Kalviainen R,
Rauramaa T,
Chassoux F,
Devaux BC,
Di Gennaro G,
Esposito V,
Bodi I,
Honavar M,
Bien CG,
Cloppenborg T,
Coras R,
Hamer HM,
Marusic P,
Kalina A,
Pieper T,
Kudernatsch M,
Hartlieb TS,
Von Oertzen TJ,
Aichholzer M,
Dorfmuller G,
Chipaux M,
Noachtar S,
Kaufmann E,
Schulze-Bonhage A,
Scheiwe CF,
Özkara C,
Grunwald T,
Koenig K,
Guerrini R,
Barba C,
Buccoliero AM,
Giordano F,
Rosenow F,
Menzler K,
Garbelli R,
Deleo F,
Krsek P,
Straka B,
Arzimanoglou AA,
Toulouse J,
Van Paesschen W,
Theys T,
Pimentel J,
Loução De Amorim IM,
Specchio N,
De Palma L,
Feucht M,
Scholl T,
Roessler K,
Toledano Delgado R,
Gil-Nagel A,
Raicevic S,
Ristic AJ,
Schijns O,
Beckervordersandforth J,
San Antonio-Arce V,
Rumia J,
Blumcke I,
Braun KP;
as the European Epilepsy Brain Bank Consortium (EEBB)</span><br />
<span class="medgenPMjournal">Neurology</span>
2024 Feb 27;102(4):e208007.
Epub 2024 Jan 30
doi: 10.1212/WNL.0000000000208007.
<span class="bold">PMID: </span><a href="/pubmed/38290094" target="_blank">38290094</a><a href="/pmc/articles/PMC10962914" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34732400">Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schon KR,
Horvath R,
Wei W,
Calabrese C,
Tucci A,
Ibañez K,
Ratnaike T,
Pitceathly RDS,
Bugiardini E,
Quinlivan R,
Hanna MG,
Clement E,
Ashton E,
Sayer JA,
Brennan P,
Josifova D,
Izatt L,
Fratter C,
Nesbitt V,
Barrett T,
McMullen DJ,
Smith A,
Deshpande C,
Smithson SF,
Festenstein R,
Canham N,
Caulfield M,
Houlden H,
Rahman S,
Chinnery PF;
Genomics England Research Consortium</span><br />
<span class="medgenPMjournal">BMJ</span>
2021 Nov 3;375:e066288.
doi: 10.1136/bmj-2021-066288.
<span class="bold">PMID: </span><a href="/pubmed/34732400" target="_blank">34732400</a><a href="/pmc/articles/PMC8565085" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29320603">Drug management for acute tonic-clonic convulsions including convulsive status epilepticus in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">McTague A,
Martland T,
Appleton R</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Jan 10;1(1):CD001905.
doi: 10.1002/14651858.CD001905.pub3.
<span class="bold">PMID: </span><a href="/pubmed/29320603" target="_blank">29320603</a><a href="/pmc/articles/PMC6491279" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/27810515">Mortality in Dravet syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cooper MS,
Mcintosh A,
Crompton DE,
McMahon JM,
Schneider A,
Farrell K,
Ganesan V,
Gill D,
Kivity S,
Lerman-Sagie T,
McLellan A,
Pelekanos J,
Ramesh V,
Sadleir L,
Wirrell E,
Scheffer IE</span><br />
<span class="medgenPMjournal">Epilepsy Res</span>
2016 Dec;128:43-47.
Epub 2016 Oct 26
doi: 10.1016/j.eplepsyres.2016.10.006.
<span class="bold">PMID: </span><a href="/pubmed/27810515" target="_blank">27810515</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Developmental%20and%20epileptic%20encephalopathy%2098%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 (99)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/34732400">Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schon KR,
Horvath R,
Wei W,
Calabrese C,
Tucci A,
Ibañez K,
Ratnaike T,
Pitceathly RDS,
Bugiardini E,
Quinlivan R,
Hanna MG,
Clement E,
Ashton E,
Sayer JA,
Brennan P,
Josifova D,
Izatt L,
Fratter C,
Nesbitt V,
Barrett T,
McMullen DJ,
Smith A,
Deshpande C,
Smithson SF,
Festenstein R,
Canham N,
Caulfield M,
Houlden H,
Rahman S,
Chinnery PF;
Genomics England Research Consortium</span><br />
<span class="medgenPMjournal">BMJ</span>
2021 Nov 3;375:e066288.
doi: 10.1136/bmj-2021-066288.
<span class="bold">PMID: </span><a href="/pubmed/34732400" target="_blank">34732400</a><a href="/pmc/articles/PMC8565085" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34374989">Spectrum of neuro-genetic disorders in the United Arab Emirates national population.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Saleh S,
Beyyumi E,
Al Kaabi A,
Hertecant J,
Barakat D,
Al Dhaheri NS,
Al-Gazali L,
Al Shamsi A</span><br />
<span class="medgenPMjournal">Clin Genet</span>
2021 Nov;100(5):573-600.
Epub 2021 Aug 19
doi: 10.1111/cge.14044.
<span class="bold">PMID: </span><a href="/pubmed/34374989" target="_blank">34374989</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33754312">Highly Purified Cannabidiol for Epilepsy Treatment: A Systematic Review of Epileptic Conditions Beyond Dravet Syndrome and Lennox-Gastaut Syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lattanzi S,
Trinka E,
Striano P,
Rocchi C,
Salvemini S,
Silvestrini M,
Brigo F</span><br />
<span class="medgenPMjournal">CNS Drugs</span>
2021 Mar;35(3):265-281.
Epub 2021 Mar 22
doi: 10.1007/s40263-021-00807-y.
<span class="bold">PMID: </span><a href="/pubmed/33754312" target="_blank">33754312</a><a href="/pmc/articles/PMC8005394" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/27581855">Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">D'Antonio F,
Pagani G,
Familiari A,
Khalil A,
Sagies TL,
Malinger G,
Leibovitz Z,
Garel C,
Moutard ML,
Pilu G,
Bhide A,
Acharya G,
Leombroni M,
Manzoli L,
Papageorghiou A,
Prefumo F</span><br />
<span class="medgenPMjournal">Pediatrics</span>
2016 Sep;138(3)
doi: 10.1542/peds.2016-0445.
<span class="bold">PMID: </span><a href="/pubmed/27581855" target="_blank">27581855</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25134878">Primary care for adults on the autism spectrum.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Nicolaidis C,
Kripke CC,
Raymaker D</span><br />
<span class="medgenPMjournal">Med Clin North Am</span>
2014 Sep;98(5):1169-91.
doi: 10.1016/j.mcna.2014.06.011.
<span class="bold">PMID: </span><a href="/pubmed/25134878" target="_blank">25134878</a><a href="/pmc/articles/PMC4851469" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Developmental%20and%20epileptic%20encephalopathy%2098%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 (74)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/38380699">L-serine treatment in patients with GRIN-related encephalopathy: a phase 2A, non-randomized study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Juliá-Palacios N,
Olivella M,
Sigatullina Bondarenko M,
Ibáñez-Micó S,
Muñoz-Cabello B,
Alonso-Luengo O,
Soto-Insuga V,
García-Navas D,
Cuesta-Herraiz L,
Andreo-Lillo P,
Aguilera-Albesa S,
Hedrera-Fernández A,
González Alguacil E,
Sánchez-Carpintero R,
Martín Del Valle F,
Jiménez González E,
Cean Cabrera L,
Medina-Rivera I,
Perez-Ordoñez M,
Colomé R,
Lopez L,
Engracia Cazorla M,
Fornaguera M,
Ormazabal A,
Alonso-Colmenero I,
Illescas KS,
Balsells-Mejía S,
Mari-Vico R,
Duffo Viñas M,
Cappuccio G,
Terrone G,
Romano R,
Manti F,
Mastrangelo M,
Alfonsi C,
de Siqueira Barros B,
Nizon M,
Gjerulfsen CE,
Muro VL,
Karall D,
Zeiner F,
Masnada S,
Peterlongo I,
Oyarzábal A,
Santos-Gómez A,
Altafaj X,
García-Cazorla Á</span><br />
<span class="medgenPMjournal">Brain</span>
2024 May 3;147(5):1653-1666.
doi: 10.1093/brain/awae041.
<span class="bold">PMID: </span><a href="/pubmed/38380699" target="_blank">38380699</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34732400">Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schon KR,
Horvath R,
Wei W,
Calabrese C,
Tucci A,
Ibañez K,
Ratnaike T,
Pitceathly RDS,
Bugiardini E,
Quinlivan R,
Hanna MG,
Clement E,
Ashton E,
Sayer JA,
Brennan P,
Josifova D,
Izatt L,
Fratter C,
Nesbitt V,
Barrett T,
McMullen DJ,
Smith A,
Deshpande C,
Smithson SF,
Festenstein R,
Canham N,
Caulfield M,
Houlden H,
Rahman S,
Chinnery PF;
Genomics England Research Consortium</span><br />
<span class="medgenPMjournal">BMJ</span>
2021 Nov 3;375:e066288.
doi: 10.1136/bmj-2021-066288.
<span class="bold">PMID: </span><a href="/pubmed/34732400" target="_blank">34732400</a><a href="/pmc/articles/PMC8565085" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33754312">Highly Purified Cannabidiol for Epilepsy Treatment: A Systematic Review of Epileptic Conditions Beyond Dravet Syndrome and Lennox-Gastaut Syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lattanzi S,
Trinka E,
Striano P,
Rocchi C,
Salvemini S,
Silvestrini M,
Brigo F</span><br />
<span class="medgenPMjournal">CNS Drugs</span>
2021 Mar;35(3):265-281.
Epub 2021 Mar 22
doi: 10.1007/s40263-021-00807-y.
<span class="bold">PMID: </span><a href="/pubmed/33754312" target="_blank">33754312</a><a href="/pmc/articles/PMC8005394" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29320603">Drug management for acute tonic-clonic convulsions including convulsive status epilepticus in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">McTague A,
Martland T,
Appleton R</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Jan 10;1(1):CD001905.
doi: 10.1002/14651858.CD001905.pub3.
<span class="bold">PMID: </span><a href="/pubmed/29320603" target="_blank">29320603</a><a href="/pmc/articles/PMC6491279" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25134878">Primary care for adults on the autism spectrum.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Nicolaidis C,
Kripke CC,
Raymaker D</span><br />
<span class="medgenPMjournal">Med Clin North Am</span>
2014 Sep;98(5):1169-91.
doi: 10.1016/j.mcna.2014.06.011.
<span class="bold">PMID: </span><a href="/pubmed/25134878" target="_blank">25134878</a><a href="/pmc/articles/PMC4851469" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Developmental%20and%20epileptic%20encephalopathy%2098%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 (46)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/34732400">Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Schon KR,
Horvath R,
Wei W,
Calabrese C,
Tucci A,
Ibañez K,
Ratnaike T,
Pitceathly RDS,
Bugiardini E,
Quinlivan R,
Hanna MG,
Clement E,
Ashton E,
Sayer JA,
Brennan P,
Josifova D,
Izatt L,
Fratter C,
Nesbitt V,
Barrett T,
McMullen DJ,
Smith A,
Deshpande C,
Smithson SF,
Festenstein R,
Canham N,
Caulfield M,
Houlden H,
Rahman S,
Chinnery PF;
Genomics England Research Consortium</span><br />
<span class="medgenPMjournal">BMJ</span>
2021 Nov 3;375:e066288.
doi: 10.1136/bmj-2021-066288.
<span class="bold">PMID: </span><a href="/pubmed/34732400" target="_blank">34732400</a><a href="/pmc/articles/PMC8565085" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32113113">Course and prognosis of adult-onset epilepsy in Brazil: A cohort study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Caprara ALF,
Rissardo JP,
Leite MTB,
Silveira JOF,
Jauris PGM,
Arend J,
Kegler A,
Royes LFF,
Fighera MR</span><br />
<span class="medgenPMjournal">Epilepsy Behav</span>
2020 Apr;105:106969.
Epub 2020 Feb 26
doi: 10.1016/j.yebeh.2020.106969.
<span class="bold">PMID: </span><a href="/pubmed/32113113" target="_blank">32113113</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31398688">The co-occurrence of epilepsy and autism: A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lukmanji S,
Manji SA,
Kadhim S,
Sauro KM,
Wirrell EC,
Kwon CS,
Jetté N</span><br />
<span class="medgenPMjournal">Epilepsy Behav</span>
2019 Sep;98(Pt A):238-248.
Epub 2019 Aug 6
doi: 10.1016/j.yebeh.2019.07.037.
<span class="bold">PMID: </span><a href="/pubmed/31398688" target="_blank">31398688</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29547159">Addition of pyridoxine to prednisolone in the treatment of infantile spasms: A pilot, randomized controlled trial.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kunnanayaka V,
Jain P,
Sharma S,
Seth A,
Aneja S</span><br />
<span class="medgenPMjournal">Neurol India</span>
2018 Mar-Apr;66(2):385-390.
doi: 10.4103/0028-3886.227281.
<span class="bold">PMID: </span><a href="/pubmed/29547159" target="_blank">29547159</a></div>
<div class="nl"><a target="_blank" href="/pubmed/27810515">Mortality in Dravet syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cooper MS,
Mcintosh A,
Crompton DE,
McMahon JM,
Schneider A,
Farrell K,
Ganesan V,
Gill D,
Kivity S,
Lerman-Sagie T,
McLellan A,
Pelekanos J,
Ramesh V,
Sadleir L,
Wirrell E,
Scheffer IE</span><br />
<span class="medgenPMjournal">Epilepsy Res</span>
2016 Dec;128:43-47.
Epub 2016 Oct 26
doi: 10.1016/j.eplepsyres.2016.10.006.
<span class="bold">PMID: </span><a href="/pubmed/27810515" target="_blank">27810515</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Developmental%20and%20epileptic%20encephalopathy%2098%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 (58)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/38380699">L-serine treatment in patients with GRIN-related encephalopathy: a phase 2A, non-randomized study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Juliá-Palacios N,
Olivella M,
Sigatullina Bondarenko M,
Ibáñez-Micó S,
Muñoz-Cabello B,
Alonso-Luengo O,
Soto-Insuga V,
García-Navas D,
Cuesta-Herraiz L,
Andreo-Lillo P,
Aguilera-Albesa S,
Hedrera-Fernández A,
González Alguacil E,
Sánchez-Carpintero R,
Martín Del Valle F,
Jiménez González E,
Cean Cabrera L,
Medina-Rivera I,
Perez-Ordoñez M,
Colomé R,
Lopez L,
Engracia Cazorla M,
Fornaguera M,
Ormazabal A,
Alonso-Colmenero I,
Illescas KS,
Balsells-Mejía S,
Mari-Vico R,
Duffo Viñas M,
Cappuccio G,
Terrone G,
Romano R,
Manti F,
Mastrangelo M,
Alfonsi C,
de Siqueira Barros B,
Nizon M,
Gjerulfsen CE,
Muro VL,
Karall D,
Zeiner F,
Masnada S,
Peterlongo I,
Oyarzábal A,
Santos-Gómez A,
Altafaj X,
García-Cazorla Á</span><br />
<span class="medgenPMjournal">Brain</span>
2024 May 3;147(5):1653-1666.
doi: 10.1093/brain/awae041.
<span class="bold">PMID: </span><a href="/pubmed/38380699" target="_blank">38380699</a></div>
<div class="nl"><a target="_blank" href="/pubmed/37951597">Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kaiyrzhanov R,
Rad A,
Lin SJ,
Bertoli-Avella A,
Kallemeijn WW,
Godwin A,
Zaki MS,
Huang K,
Lau T,
Petree C,
Efthymiou S,
Karimiani EG,
Hempel M,
Normand EA,
Rudnik-Schöneborn S,
Schatz UA,
Baggelaar MP,
Ilyas M,
Sultan T,
Alvi JR,
Ganieva M,
Fowler B,
Aanicai R,
Tayfun GA,
Al Saman A,
Alswaid A,
Amiri N,
Asilova N,
Shotelersuk V,
Yeetong P,
Azam M,
Babaei M,
Monajemi GB,
Mohammadi P,
Samie S,
Banu SH,
Pinto Basto J,
Kortüm F,
Bauer M,
Bauer P,
Beetz C,
Garshasbi M,
Issa AH,
Eyaid W,
Ahmed H,
Hashemi N,
Hassanpour K,
Herman I,
Ibrohimov S,
Abdul-Majeed BA,
Imdad M,
Isrofilov M,
Kaiyal Q,
Khan S,
Kirmse B,
Koster J,
Lourenço CM,
Mitani T,
Moldovan O,
Murphy D,
Najafi M,
Pehlivan D,
Rocha ME,
Salpietro V,
Schmidts M,
Shalata A,
Mahroum M,
Talbeya JK,
Taylor RW,
Vazquez D,
Vetro A,
Waterham HR,
Zaman M,
Schrader TA,
Chung WK,
Guerrini R,
Lupski JR,
Gleeson J,
Suri M,
Jamshidi Y,
Bhatia KP,
Vona B,
Schrader M,
Severino M,
Guille M,
Tate EW,
Varshney GK,
Houlden H,
Maroofian R</span><br />
<span class="medgenPMjournal">Brain</span>
2024 Apr 4;147(4):1436-1456.
doi: 10.1093/brain/awad380.
<span class="bold">PMID: </span><a href="/pubmed/37951597" target="_blank">37951597</a><a href="/pmc/articles/PMC10994533" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33754312">Highly Purified Cannabidiol for Epilepsy Treatment: A Systematic Review of Epileptic Conditions Beyond Dravet Syndrome and Lennox-Gastaut Syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lattanzi S,
Trinka E,
Striano P,
Rocchi C,
Salvemini S,
Silvestrini M,
Brigo F</span><br />
<span class="medgenPMjournal">CNS Drugs</span>
2021 Mar;35(3):265-281.
Epub 2021 Mar 22
doi: 10.1007/s40263-021-00807-y.
<span class="bold">PMID: </span><a href="/pubmed/33754312" target="_blank">33754312</a><a href="/pmc/articles/PMC8005394" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29320603">Drug management for acute tonic-clonic convulsions including convulsive status epilepticus in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">McTague A,
Martland T,
Appleton R</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Jan 10;1(1):CD001905.
doi: 10.1002/14651858.CD001905.pub3.
<span class="bold">PMID: </span><a href="/pubmed/29320603" target="_blank">29320603</a><a href="/pmc/articles/PMC6491279" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/27581855">Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">D'Antonio F,
Pagani G,
Familiari A,
Khalil A,
Sagies TL,
Malinger G,
Leibovitz Z,
Garel C,
Moutard ML,
Pilu G,
Bhide A,
Acharya G,
Leombroni M,
Manzoli L,
Papageorghiou A,
Prefumo F</span><br />
<span class="medgenPMjournal">Pediatrics</span>
2016 Sep;138(3)
doi: 10.1542/peds.2016-0445.
<span class="bold">PMID: </span><a href="/pubmed/27581855" target="_blank">27581855</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Developmental%20and%20epileptic%20encephalopathy%2098%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 (71)</a></div></div>
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<div class="nl"><a target="_blank" href="/pubmed/37023554">The influence of disease course and surgery on quality of life in children with focal cortical dysplasia and long-term epilepsy-associated tumours: A systematic review and meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vasilica AM,
Winsor A,
Chari A,
Scott R,
Baldeweg T,
Tisdall M</span><br />
<span class="medgenPMjournal">Epilepsy Res</span>
2023 May;192:107132.
Epub 2023 Mar 30
doi: 10.1016/j.eplepsyres.2023.107132.
<span class="bold">PMID: </span><a href="/pubmed/37023554" target="_blank">37023554</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35034187">Efficacy and safety of VNS therapy or continued medication management for treatment of adults with drug-resistant epilepsy: systematic review and meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Batson S,
Shankar R,
Conry J,
Boggs J,
Radtke R,
Mitchell S,
Barion F,
Murphy J,
Danielson V</span><br />
<span class="medgenPMjournal">J Neurol</span>
2022 Jun;269(6):2874-2891.
Epub 2022 Jan 16
doi: 10.1007/s00415-022-10967-6.
<span class="bold">PMID: </span><a href="/pubmed/35034187" target="_blank">35034187</a><a href="/pmc/articles/PMC9119900" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33754312">Highly Purified Cannabidiol for Epilepsy Treatment: A Systematic Review of Epileptic Conditions Beyond Dravet Syndrome and Lennox-Gastaut Syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lattanzi S,
Trinka E,
Striano P,
Rocchi C,
Salvemini S,
Silvestrini M,
Brigo F</span><br />
<span class="medgenPMjournal">CNS Drugs</span>
2021 Mar;35(3):265-281.
Epub 2021 Mar 22
doi: 10.1007/s40263-021-00807-y.
<span class="bold">PMID: </span><a href="/pubmed/33754312" target="_blank">33754312</a><a href="/pmc/articles/PMC8005394" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31398688">The co-occurrence of epilepsy and autism: A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lukmanji S,
Manji SA,
Kadhim S,
Sauro KM,
Wirrell EC,
Kwon CS,
Jetté N</span><br />
<span class="medgenPMjournal">Epilepsy Behav</span>
2019 Sep;98(Pt A):238-248.
Epub 2019 Aug 6
doi: 10.1016/j.yebeh.2019.07.037.
<span class="bold">PMID: </span><a href="/pubmed/31398688" target="_blank">31398688</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29320603">Drug management for acute tonic-clonic convulsions including convulsive status epilepticus in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">McTague A,
Martland T,
Appleton R</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Jan 10;1(1):CD001905.
doi: 10.1002/14651858.CD001905.pub3.
<span class="bold">PMID: </span><a href="/pubmed/29320603" target="_blank">29320603</a><a href="/pmc/articles/PMC6491279" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Developmental%20and%20epileptic%20encephalopathy%2098%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (9)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C5562017%5bDISCUI%5d&amp;filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (3)</a></li>
<li><a href="/gtr/tests?term=C5562017%5bDISCUI%5d&amp;filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (5)</a></li>
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C5562017%5bDISCUI%5d" target="_blank">See all (5)</a></total></li>
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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=(developmental%20and%20epileptic%20encephalopathy%2098)%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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