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<meta name="keywords" content="C4023354, abnormal central motor function, abnormality of central motor function, pathologic function, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="An anomaly of the control or production of movement in the central nervous system." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=868940
|
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ConceptID=C4023354
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormal central motor function</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>868940</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.">C4023354</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Abnormality of central motor function</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:0011442">HP:0011442</a></td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln">An anomaly of the control or production of movement in the central nervous system. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="TLline">Abnormal central motor function</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/871309" ref="tree=MeSH" title="MedGen record for Abnormality of prenatal development or birth">Abnormality of prenatal development or birth</a></span><ul><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/868417" ref="tree=MeSH" title="MedGen record for Abnormal nervous system physiology">Abnormal nervous system physiology</a></span><ul><li><span class="matched_ds">Abnormal central motor function</span><ul><li><span class="TLline"><a href="/medgen/868654" ref="tree=MeSH" title="MedGen record for Abnormality of central motor conduction">Abnormality of central motor conduction</a></span><ul><li><span class="TLline"><a href="/medgen/908394" ref="tree=MeSH" title="MedGen record for Prolonged central motor conduction time">Prolonged central motor conduction time</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/868939" ref="tree=MeSH" title="MedGen record for Abnormality of coordination">Abnormality of coordination</a></span><ul><li><span class="TLline"><a href="/medgen/849" ref="tree=MeSH" title="MedGen record for Cerebellar ataxia">Cerebellar ataxia</a></span><ul><li><span class="TLline"><a href="/medgen/115975" ref="tree=MeSH" title="MedGen record for Dysdiadochokinesis">Dysdiadochokinesis</a></span></li><li><span class="TLline"><a href="/medgen/68583" ref="tree=MeSH" title="MedGen record for Dysmetria">Dysmetria</a></span></li><li><span class="TLline"><a href="/medgen/13945" ref="tree=MeSH" title="MedGen record for Dyssynergia">Dyssynergia</a></span></li><li><span class="TLline"><a href="/medgen/314033" ref="tree=MeSH" title="MedGen record for Hereditary episodic ataxia">Hereditary episodic ataxia</a></span></li><li><span class="TLline"><a href="/medgen/196692" ref="tree=MeSH" title="MedGen record for Limb ataxia">Limb ataxia</a></span></li><li><span class="TLline"><a href="/medgen/335079" ref="tree=MeSH" title="MedGen record for Nonprogressive cerebellar ataxia">Nonprogressive cerebellar ataxia</a></span></li><li><span class="TLline"><a href="/medgen/1635801" ref="tree=MeSH" title="MedGen record for Optic ataxia">Optic ataxia</a></span></li><li><span class="TLline"><a href="/medgen/140727" ref="tree=MeSH" title="MedGen record for Progressive cerebellar ataxia">Progressive cerebellar ataxia</a></span></li><li><span class="TLline"><a href="/medgen/376528" ref="tree=MeSH" title="MedGen record for Spastic ataxia">Spastic ataxia</a></span></li><li><span class="TLline"><a href="/medgen/39733" ref="tree=MeSH" title="MedGen record for Spinocerebellar atrophy">Spinocerebellar atrophy</a></span></li><li><span class="TLline"><a href="/medgen/96535" ref="tree=MeSH" title="MedGen record for Truncal ataxia">Truncal ataxia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/141714" ref="tree=MeSH" title="MedGen record for Incoordination">Incoordination</a></span><ul><li><span class="TLline"><a href="/medgen/66690" ref="tree=MeSH" title="MedGen record for Clumsiness">Clumsiness</a></span></li><li><span class="TLline"><a href="/medgen/107874" ref="tree=MeSH" title="MedGen record for Poor coordination">Poor coordination</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/892716" ref="tree=MeSH" title="MedGen record for Motor impersistence">Motor impersistence</a></span><ul><li><span class="TLline"><a href="/medgen/893106" ref="tree=MeSH" title="MedGen record for Simultanapraxia">Simultanapraxia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/338471" ref="tree=MeSH" title="MedGen record for Poor motor coordination">Poor motor coordination</a></span><ul><li><span class="TLline"><a href="/medgen/356863" ref="tree=MeSH" title="MedGen record for Poor fine motor coordination">Poor fine motor coordination</a></span></li><li><span class="TLline"><a href="/medgen/641383" ref="tree=MeSH" title="MedGen record for Poor gross motor coordination">Poor gross motor coordination</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/65885" ref="tree=MeSH" title="MedGen record for Slurred speech">Slurred speech</a></span><ul><li><span class="TLline"><a href="/medgen/870482" ref="tree=MeSH" title="MedGen record for Slowed slurred speech">Slowed slurred speech</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/115941" ref="tree=MeSH" title="MedGen record for Abnormality of extrapyramidal motor function">Abnormality of extrapyramidal motor function</a></span><ul><li><span class="TLline"><a href="/medgen/115925" ref="tree=MeSH" title="MedGen record for Bradykinesia">Bradykinesia</a></span></li><li><span class="TLline"><a href="/medgen/329357" ref="tree=MeSH" title="MedGen record for Exaggerated startle response">Exaggerated startle response</a></span></li><li><span class="TLline"><a href="/medgen/343817" ref="tree=MeSH" title="MedGen record for Extrapyramidal muscular rigidity">Extrapyramidal muscular rigidity</a></span><ul><li><span class="TLline"><a href="/medgen/867222" ref="tree=MeSH" title="MedGen record for Progressive extrapyramidal muscular rigidity">Progressive extrapyramidal muscular rigidity</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/66079" ref="tree=MeSH" title="MedGen record for Parkinsonian disorder">Parkinsonian disorder</a></span><ul><li><span class="TLline"><a href="/medgen/199874" ref="tree=MeSH" title="MedGen record for Lewy body dementia">Lewy body dementia</a></span></li><li><span class="TLline"><a href="/medgen/10590" ref="tree=MeSH" title="MedGen record for Parkinson disease">Parkinson disease</a></span></li><li><span class="TLline"><a href="/medgen/375989" ref="tree=MeSH" title="MedGen record for Parkinsonism with favorable response to dopaminergic medication">Parkinsonism with favorable response to dopaminergic medication</a></span></li><li><span class="TLline"><a href="/medgen/10592" ref="tree=MeSH" title="MedGen record for Secondary Parkinson disease">Secondary Parkinson disease</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/411258" ref="tree=MeSH" title="MedGen record for Progressive extrapyramidal movement disorder">Progressive extrapyramidal movement disorder</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/8166" ref="tree=MeSH" title="MedGen record for Apraxia">Apraxia</a></span><ul><li><span class="TLline"><a href="/medgen/404626" ref="tree=MeSH" title="MedGen record for Alien Hand Syndrome">Alien Hand Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/266930" ref="tree=MeSH" title="MedGen record for Gait apraxia">Gait apraxia</a></span></li><li><span class="TLline"><a href="/medgen/1715739" ref="tree=MeSH" title="MedGen record for Hand apraxia">Hand apraxia</a></span></li><li><span class="TLline"><a href="/medgen/115961" ref="tree=MeSH" title="MedGen record for Ideomotor apraxia">Ideomotor apraxia</a></span></li><li><span class="TLline"><a href="/medgen/868182" ref="tree=MeSH" title="MedGen record for Limb apraxia">Limb apraxia</a></span></li><li><span class="TLline"><a href="/medgen/483686" ref="tree=MeSH" title="MedGen record for Oculomotor apraxia">Oculomotor apraxia</a></span></li><li><span class="TLline"><a href="/medgen/867468" ref="tree=MeSH" title="MedGen record for Oromotor apraxia">Oromotor apraxia</a></span></li><li><span class="TLline"><a href="/medgen/78112" ref="tree=MeSH" title="MedGen record for Speech apraxia">Speech apraxia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/2862" ref="tree=MeSH" title="MedGen record for Cataplexy">Cataplexy</a></span></li><li><span class="TLline"><a href="/medgen/1053170" ref="tree=MeSH" title="MedGen record for crossed brainstem sign">crossed brainstem sign</a></span></li><li><span class="TLline"><a href="/medgen/1813865" ref="tree=MeSH" title="MedGen record for Involuntary vocalization">Involuntary vocalization</a></span><ul><li><span class="TLline"><a href="/medgen/1863920" ref="tree=MeSH" title="MedGen record for Continuous involuntary vocalizations">Continuous involuntary vocalizations</a></span></li><li><span class="TLline"><a href="/medgen/68575" ref="tree=MeSH" title="MedGen record for Coprolalia">Coprolalia</a></span></li><li><span class="TLline"><a href="/medgen/8532" ref="tree=MeSH" title="MedGen record for Echolalia">Echolalia</a></span><ul><li><span class="TLline"><a href="/medgen/1841793" ref="tree=MeSH" title="MedGen record for Delayed Echolalia">Delayed Echolalia</a></span></li><li><span class="TLline"><a href="/medgen/1841920" ref="tree=MeSH" title="MedGen record for Immediate Echolalia">Immediate Echolalia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1863439" ref="tree=MeSH" title="MedGen record for Klazomania">Klazomania</a></span></li><li><span class="TLline"><a href="/medgen/581078" ref="tree=MeSH" title="MedGen record for Palilalia">Palilalia</a></span></li><li><span class="TLline"><a href="/medgen/155955" ref="tree=MeSH" title="MedGen record for Phonic tics">Phonic tics</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/105510" ref="tree=MeSH" title="MedGen record for Paralysis">Paralysis</a></span><ul><li><span class="TLline"><a href="/medgen/473191" ref="tree=MeSH" title="MedGen record for Brachial Plexus Palsy">Brachial Plexus Palsy</a></span><ul><li><span class="TLline"><a href="/medgen/124376" ref="tree=MeSH" title="MedGen record for Klumpke-Déjerine paralysis">Klumpke-Déjerine paralysis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/5101" ref="tree=MeSH" title="MedGen record for Facial paralysis">Facial paralysis</a></span><ul><li><span class="TLline"><a href="/medgen/859714" ref="tree=MeSH" title="MedGen record for Acquired Facial Nerve Palsy">Acquired Facial Nerve Palsy</a></span></li><li><span class="TLline"><a href="/medgen/581580" ref="tree=MeSH" title="MedGen record for Congenital facial nerve palsy">Congenital facial nerve palsy</a></span></li><li><span class="TLline"><a href="/medgen/858754" ref="tree=MeSH" title="MedGen record for Facial Nerve Palsy Related to Birth">Facial Nerve Palsy Related to Birth</a></span></li><li><span class="TLline"><a href="/medgen/768724" ref="tree=MeSH" title="MedGen record for Facial Nerve Palsy Related to Trauma">Facial Nerve Palsy Related to Trauma</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/101809" ref="tree=MeSH" title="MedGen record for Gastroparesis">Gastroparesis</a></span></li><li><span class="TLline"><a href="/medgen/9196" ref="tree=MeSH" title="MedGen record for Hemiplegia">Hemiplegia</a></span><ul><li><span class="TLline"><a href="/medgen/350828" ref="tree=MeSH" title="MedGen record for Episodic hemiplegia">Episodic hemiplegia</a></span></li><li><span class="TLline"><a href="/medgen/630098" ref="tree=MeSH" title="MedGen record for Left hemiplegia">Left hemiplegia</a></span></li><li><span class="TLline"><a href="/medgen/630097" ref="tree=MeSH" title="MedGen record for Right hemiplegia">Right hemiplegia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/45205" ref="tree=MeSH" title="MedGen record for Ophthalmoplegia">Ophthalmoplegia</a></span><ul><li><span class="TLline"><a href="/medgen/57662" ref="tree=MeSH" title="MedGen record for External ophthalmoplegia">External ophthalmoplegia</a></span></li><li><span class="TLline"><a href="/medgen/137925" ref="tree=MeSH" title="MedGen record for Internal ophthalmoplegia">Internal ophthalmoplegia</a></span></li><li><span class="TLline"><a href="/medgen/101820" ref="tree=MeSH" title="MedGen record for Internuclear ophthalmoplegia">Internuclear ophthalmoplegia</a></span></li><li><span class="TLline"><a href="/medgen/102439" ref="tree=MeSH" title="MedGen record for Progressive external ophthalmoplegia">Progressive external ophthalmoplegia</a></span></li><li><span class="TLline"><a href="/medgen/384479" ref="tree=MeSH" title="MedGen record for Progressive ophthalmoplegia">Progressive ophthalmoplegia</a></span></li><li><span class="TLline"><a href="/medgen/21026" ref="tree=MeSH" title="MedGen record for Progressive supranuclear palsy">Progressive supranuclear palsy</a></span></li><li><span class="TLline"><a href="/medgen/452212" ref="tree=MeSH" title="MedGen record for Recurrent painful ophthalmoplegic neuropathy">Recurrent painful ophthalmoplegic neuropathy</a></span></li><li><span class="TLline"><a href="/medgen/235616" ref="tree=MeSH" title="MedGen record for Supranuclear ophthalmoplegia">Supranuclear ophthalmoplegia</a></span></li><li><span class="TLline"><a href="/medgen/57604" ref="tree=MeSH" title="MedGen record for Total ophthalmoplegia">Total ophthalmoplegia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/45323" ref="tree=MeSH" title="MedGen record for Paraplegia">Paraplegia</a></span><ul><li><span class="TLline"><a href="/medgen/69225" ref="tree=MeSH" title="MedGen record for Brown-Séquard syndrome">Brown-Séquard syndrome</a></span></li><li><span class="TLline"><a href="/medgen/20882" ref="tree=MeSH" title="MedGen record for Spastic paraplegia">Spastic paraplegia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10589" ref="tree=MeSH" title="MedGen record for Paresis">Paresis</a></span><ul><li><span class="TLline"><a href="/medgen/6783" ref="tree=MeSH" title="MedGen record for Hemiparesis">Hemiparesis</a></span></li><li><span class="TLline"><a href="/medgen/113150" ref="tree=MeSH" title="MedGen record for Paraparesis">Paraparesis</a></span></li><li><span class="TLline"><a href="/medgen/78089" ref="tree=MeSH" title="MedGen record for Paresis of extraocular muscles">Paresis of extraocular muscles</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/488958" ref="tree=MeSH" title="MedGen record for Periodic paralysis">Periodic paralysis</a></span><ul><li><span class="TLline"><a href="/medgen/327586" ref="tree=MeSH" title="MedGen record for Andersen Tawil syndrome">Andersen Tawil syndrome</a></span></li><li><span class="TLline"><a href="/medgen/68665" ref="tree=MeSH" title="MedGen record for Hyperkalemic periodic paralysis">Hyperkalemic periodic paralysis</a></span></li><li><span class="TLline"><a href="/medgen/116058" ref="tree=MeSH" title="MedGen record for Hypokalemic periodic paralysis">Hypokalemic periodic paralysis</a></span></li><li><span class="TLline"><a href="/medgen/867195" ref="tree=MeSH" title="MedGen record for Periodic hypokalemic paresis">Periodic hypokalemic paresis</a></span></li><li><span class="TLline"><a href="/medgen/1670241" ref="tree=MeSH" title="MedGen record for Periodic paralysis with later-onset distal motor neuropathy">Periodic paralysis with later-onset distal motor neuropathy</a></span></li><li><span class="TLline"><a href="/medgen/1668303" ref="tree=MeSH" title="MedGen record for Periodic paralysis with transient compartment-like syndrome">Periodic paralysis with transient compartment-like syndrome</a></span></li><li><span class="TLline"><a href="/medgen/120639" ref="tree=MeSH" title="MedGen record for Thyrotoxic periodic paralysis">Thyrotoxic periodic paralysis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10989" ref="tree=MeSH" title="MedGen record for Pseudobulbar paralysis">Pseudobulbar paralysis</a></span></li><li><span class="TLline"><a href="/medgen/19748" ref="tree=MeSH" title="MedGen record for Respiratory paralysis">Respiratory paralysis</a></span></li><li><span class="TLline"><a href="/medgen/19617" ref="tree=MeSH" title="MedGen record for Tetraplegia">Tetraplegia</a></span><ul><li><span class="TLline"><a href="/medgen/350829" ref="tree=MeSH" title="MedGen record for Episodic quadriplegia">Episodic quadriplegia</a></span></li><li><span class="TLline"><a href="/medgen/7378" ref="tree=MeSH" title="MedGen record for Locked-in syndrome">Locked-in syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/53047" ref="tree=MeSH" title="MedGen record for Vocal cord paralysis">Vocal cord paralysis</a></span><ul><li><span class="TLline"><a href="/medgen/833874" ref="tree=MeSH" title="MedGen record for Bilateral vocal cord paralysis">Bilateral vocal cord paralysis</a></span></li><li><span class="TLline"><a href="/medgen/155887" ref="tree=MeSH" title="MedGen record for Unilateral vocal cord paralysis">Unilateral vocal cord paralysis</a></span></li><li><span class="TLline"><a href="/medgen/155888" ref="tree=MeSH" title="MedGen record for Vocal cord paresis">Vocal cord paresis</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/333241" ref="tree=MeSH" title="MedGen record for Upper motor neuron dysfunction">Upper motor neuron dysfunction</a></span><ul><li><span class="TLline"><a href="/medgen/68582" ref="tree=MeSH" title="MedGen record for Abnormal pyramidal sign">Abnormal pyramidal sign</a></span><ul><li><span class="TLline"><a href="/medgen/451083" ref="tree=MeSH" title="MedGen record for Chaddock reflex">Chaddock reflex</a></span></li><li><span class="TLline"><a href="/medgen/866701" ref="tree=MeSH" title="MedGen record for Gordon reflex">Gordon reflex</a></span></li><li><span class="TLline"><a href="/medgen/78828" ref="tree=MeSH" title="MedGen record for Hoffmann sign">Hoffmann sign</a></span></li><li><span class="TLline"><a href="/medgen/735510" ref="tree=MeSH" title="MedGen record for Oppenheim reflex">Oppenheim reflex</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/322009" ref="tree=MeSH" title="MedGen record for Dysfunction of lateral corticospinal tracts">Dysfunction of lateral corticospinal tracts</a></span></li><li><span class="TLline"><a href="/medgen/7753" ref="tree=MeSH" title="MedGen record for Spasticity">Spasticity</a></span><ul><li><span class="TLline"><a href="/medgen/937224" ref="tree=MeSH" title="MedGen record for Appendicular spasticity">Appendicular spasticity</a></span></li><li><span class="TLline"><a href="/medgen/56246" ref="tree=MeSH" title="MedGen record for Opisthotonus">Opisthotonus</a></span></li><li><span class="TLline"><a href="/medgen/347171" ref="tree=MeSH" title="MedGen record for Progressive spasticity">Progressive spasticity</a></span></li><li><span class="TLline"><a href="/medgen/344036" ref="tree=MeSH" title="MedGen record for Spasticity of facial muscles">Spasticity of facial muscles</a></span></li><li><span class="TLline"><a href="/medgen/342872" ref="tree=MeSH" title="MedGen record for Spasticity of pharyngeal muscles">Spasticity of pharyngeal muscles</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/866899" ref="tree=MeSH" title="MedGen record for Weakness due to upper motor neuron dysfunction">Weakness due to upper motor neuron dysfunction</a></span><ul><li><span class="TLline"><a href="/medgen/852561" ref="tree=MeSH" title="MedGen record for Hemiplegia/hemiparesis">Hemiplegia/hemiparesis</a></span></li><li><span class="TLline"><a href="/medgen/869366" ref="tree=MeSH" title="MedGen record for Paraplegia/paraparesis">Paraplegia/paraparesis</a></span></li><li><span class="TLline"><a href="/medgen/868203" ref="tree=MeSH" title="MedGen record for Tetraplegia/tetraparesis">Tetraplegia/tetraparesis</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</div>
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<div class="portlet mgSection" id="ID_105">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
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<div class="nl"><a target="_blank" href="/pubmed/33651094">Diagnosis and Treatment of Irritable Bowel Syndrome: A Review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Camilleri M</span><br />
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<span class="medgenPMjournal">JAMA</span>
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||
2021 Mar 2;325(9):865-877.
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||
doi: 10.1001/jama.2020.22532.
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||
<span class="bold">PMID: </span><a href="/pubmed/33651094" target="_blank">33651094</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/27585961">Diagnosis and management of Silver-Russell syndrome: first international consensus statement.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wakeling EL,
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Brioude F,
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Lokulo-Sodipe O,
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||
O'Connell SM,
|
||
Salem J,
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||
Bliek J,
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Canton AP,
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Chrzanowska KH,
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Davies JH,
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Dias RP,
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Dubern B,
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Elbracht M,
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Giabicani E,
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||
Grimberg A,
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Grønskov K,
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Hokken-Koelega AC,
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Jorge AA,
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Kagami M,
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Linglart A,
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Maghnie M,
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Mohnike K,
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Monk D,
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Moore GE,
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Murray PG,
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Ogata T,
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Petit IO,
|
||
Russo S,
|
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Said E,
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Toumba M,
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Tümer Z,
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Binder G,
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||
Eggermann T,
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||
Harbison MD,
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||
Temple IK,
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||
Mackay DJ,
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||
Netchine I</span><br />
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<span class="medgenPMjournal">Nat Rev Endocrinol</span>
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2017 Feb;13(2):105-124.
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||
Epub 2016 Sep 2
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||
doi: 10.1038/nrendo.2016.138.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27585961" target="_blank">27585961</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26474316">MDS clinical diagnostic criteria for Parkinson's disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Postuma RB,
|
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Berg D,
|
||
Stern M,
|
||
Poewe W,
|
||
Olanow CW,
|
||
Oertel W,
|
||
Obeso J,
|
||
Marek K,
|
||
Litvan I,
|
||
Lang AE,
|
||
Halliday G,
|
||
Goetz CG,
|
||
Gasser T,
|
||
Dubois B,
|
||
Chan P,
|
||
Bloem BR,
|
||
Adler CH,
|
||
Deuschl G</span><br />
|
||
<span class="medgenPMjournal">Mov Disord</span>
|
||
2015 Oct;30(12):1591-601.
|
||
doi: 10.1002/mds.26424.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26474316" target="_blank">26474316</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20central%20motor%20function)%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 (99)</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/35150573">Approach to the Patient With Prader-Willi Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Höybye C,
|
||
Tauber M</span><br />
|
||
<span class="medgenPMjournal">J Clin Endocrinol Metab</span>
|
||
2022 May 17;107(6):1698-1705.
|
||
doi: 10.1210/clinem/dgac082.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35150573" target="_blank">35150573</a><a href="/pmc/articles/PMC9635059" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35150089">A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Duis J,
|
||
Nespeca M,
|
||
Summers J,
|
||
Bird L,
|
||
Bindels-de Heus KGCB,
|
||
Valstar MJ,
|
||
de Wit MY,
|
||
Navis C,
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Katyayan A,
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Nangia S,
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Thibert R,
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Glaze D,
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Pelc K,
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Simon N,
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Sadhwani A,
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Heussler H,
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Wheeler A,
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Woeber C,
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DeRamus M,
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Thomas A,
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Kertcher E,
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DeValk L,
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Kalemeris K,
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Arps K,
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Baym C,
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Harris N,
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Gorham JP,
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Bohnsack BL,
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Chambers RC,
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Harris S,
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Chambers HG,
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Okoniewski K,
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<div class="nl"><a target="_blank" href="/pubmed/31261106">Gait Characteristics of Children Born Preterm.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Albesher RA,
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Spittle AJ,
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McGinley JL,
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2019 Jul;20(7):e397-e408.
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<div class="nl"><a target="_blank" href="/pubmed/27585961">Diagnosis and management of Silver-Russell syndrome: first international consensus statement.</a></div>
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Brioude F,
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Lokulo-Sodipe O,
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O'Connell SM,
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Salem J,
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Bliek J,
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Canton AP,
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Chrzanowska KH,
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Davies JH,
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Dias RP,
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Dubern B,
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Elbracht M,
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Giabicani E,
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Grimberg A,
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Grønskov K,
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Hokken-Koelega AC,
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Jorge AA,
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Kagami M,
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Linglart A,
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Maghnie M,
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Mohnike K,
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Monk D,
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Moore GE,
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Murray PG,
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Ogata T,
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Petit IO,
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Russo S,
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Said E,
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Toumba M,
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Tümer Z,
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Binder G,
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Eggermann T,
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Harbison MD,
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Temple IK,
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Mackay DJ,
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Netchine I</span><br />
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Brioude F,
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Lokulo-Sodipe O,
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O'Connell SM,
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Salem J,
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Bliek J,
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Canton AP,
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Chrzanowska KH,
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Davies JH,
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Dias RP,
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Dubern B,
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Elbracht M,
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Giabicani E,
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Grimberg A,
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Linglart A,
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Maghnie M,
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Mohnike K,
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Monk D,
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Moore GE,
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Murray PG,
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Ogata T,
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Petit IO,
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Russo S,
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Said E,
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Toumba M,
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Tümer Z,
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Binder G,
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Eggermann T,
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Harbison MD,
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Temple IK,
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Mackay DJ,
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Netchine I</span><br />
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2017 Feb;13(2):105-124.
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Epub 2016 Sep 2
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<span class="bold">PMID: </span><a href="/pubmed/27585961" target="_blank">27585961</a></div>
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doi: 10.1055/s-0037-1601449.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28561207" target="_blank">28561207</a><a href="/pmc/articles/PMC5985975" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26592778">Computational motor control as a window to understanding schizophrenia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Izawa J,
|
||
Asai T,
|
||
Imamizu H</span><br />
|
||
<span class="medgenPMjournal">Neurosci Res</span>
|
||
2016 Mar;104:44-51.
|
||
Epub 2015 Nov 22
|
||
doi: 10.1016/j.neures.2015.11.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26592778" target="_blank">26592778</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25238977">Simpson-Golabi-Behmel syndrome types I and II.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tenorio J,
|
||
Arias P,
|
||
Martínez-Glez V,
|
||
Santos F,
|
||
García-Miñaur S,
|
||
Nevado J,
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||
Lapunzina P</span><br />
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<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2014 Sep 20;9:138.
|
||
doi: 10.1186/s13023-014-0138-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25238977" target="_blank">25238977</a><a href="/pmc/articles/PMC4254265" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18795595">Central motor and sensory pathway involvement in an X-linked Charcot-Marie-Tooth family.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zambelis T,
|
||
Panas M,
|
||
Kokotis P,
|
||
Karadima G,
|
||
Kararizou E,
|
||
Karandreas N</span><br />
|
||
<span class="medgenPMjournal">Acta Neurol Belg</span>
|
||
2008 Jun;108(2):44-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18795595" target="_blank">18795595</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18690497">Neurophysiological markers.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leocani L,
|
||
Comi G</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2008 Sep;29 Suppl 2:S218-21.
|
||
doi: 10.1007/s10072-008-0942-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18690497" target="_blank">18690497</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20central%20motor%20function%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 (965)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/38703861">Biomarkers of mitochondrial dysfunction in autism spectrum disorder: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Frye RE,
|
||
Rincon N,
|
||
McCarty PJ,
|
||
Brister D,
|
||
Scheck AC,
|
||
Rossignol DA</span><br />
|
||
<span class="medgenPMjournal">Neurobiol Dis</span>
|
||
2024 Jul;197:106520.
|
||
Epub 2024 May 3
|
||
doi: 10.1016/j.nbd.2024.106520.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38703861" target="_blank">38703861</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28755534">Treadmill interventions in children under six years of age at risk of neuromotor delay.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Valentín-Gudiol M,
|
||
Mattern-Baxter K,
|
||
Girabent-Farrés M,
|
||
Bagur-Calafat C,
|
||
Hadders-Algra M,
|
||
Angulo-Barroso RM</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2017 Jul 29;7(7):CD009242.
|
||
doi: 10.1002/14651858.CD009242.pub3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28755534" target="_blank">28755534</a><a href="/pmc/articles/PMC6483121" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27149418">Corticosteroids for the treatment of Duchenne muscular dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matthews E,
|
||
Brassington R,
|
||
Kuntzer T,
|
||
Jichi F,
|
||
Manzur AY</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2016 May 5;2016(5):CD003725.
|
||
doi: 10.1002/14651858.CD003725.pub4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27149418" target="_blank">27149418</a><a href="/pmc/articles/PMC8580515" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26597166">Early developmental intervention programmes provided post hospital discharge to prevent motor and cognitive impairment in preterm infants.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Spittle A,
|
||
Orton J,
|
||
Anderson PJ,
|
||
Boyd R,
|
||
Doyle LW</span><br />
|
||
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
|
||
2015 Nov 24;2015(11):CD005495.
|
||
doi: 10.1002/14651858.CD005495.pub4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26597166" target="_blank">26597166</a><a href="/pmc/articles/PMC8612699" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23406512">Systematic review of central nervous system anomalies in incontinentia pigmenti.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Minić S,
|
||
Trpinac D,
|
||
Obradović M</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2013 Feb 13;8:25.
|
||
doi: 10.1186/1750-1172-8-25.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23406512" target="_blank">23406512</a><a href="/pmc/articles/PMC3576363" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20central%20motor%20function%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 (43)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
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|
||
<div class=" bottom">
|
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|
||
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|
||
|
||
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|
||
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|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
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|
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|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Abnormal%20central%20motor%20function" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20central%20motor%20function)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Abnormal%20central%20motor%20function%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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<a href="/pubmed/clinical?term=Abnormal%20central%20motor%20function" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Abnormal%20central%20motor%20function%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=868940" ref="log$=recordlinks">ClinVar</a>
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" cmd="ClearHT" href="?cmd=ClearHT&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory">
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" class="HTOn" cmd="HTOff" href="?cmd=HTOff&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d3dc2967c23b31e0b6eb42">Abnormal central motor function</a>
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<div class="ralinkpop offscreen_noflow">Abnormal central motor function<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d3dc2667c23b31e0b6dd32">Episodic ataxia type 7</a>
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<div class="ralinkpop offscreen_noflow">Episodic ataxia type 7<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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</li>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d3dc222f30673f7bfec884">Episodic ataxia type 6</a>
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<div class="ralinkpop offscreen_noflow">Episodic ataxia type 6<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=4" href="/portal/utils/pageresolver.fcgi?recordid=67d3dc1d67c23b31e0b6a1b0">Episodic ataxia type 5</a>
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<div class="ralinkpop offscreen_noflow">Episodic ataxia type 5<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=5" href="/portal/utils/pageresolver.fcgi?recordid=67d3dc1784f3725e594317ef">Episodic ataxia type 4</a>
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