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<meta name="keywords" content="C4024710, cerebellar cortex degeneration, cerebellar cortical atrophy, cortical and cerebellar atrophy, 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="Atrophy (wasting) of the cerebellar cortex." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Cerebellar cortical atrophy</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>870270</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.">C4024710</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
<td>Cortical and cerebellar atrophy</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:0008278">HP:0008278</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>
<div class="portlet_content ln">Atrophy (wasting) of the cerebellar cortex. [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_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test,  </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test,  </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM,  </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>,  </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar  </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="TLline">Cerebellar cortical atrophy</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/892343" ref="tree=MeSH" title="MedGen record for Morphological central nervous system abnormality">Morphological central nervous system abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/866738" ref="tree=MeSH" title="MedGen record for Abnormal brain morphology">Abnormal brain morphology</a></span><ul><li><span class="TLline"><a href="/medgen/866816" ref="tree=MeSH" title="MedGen record for Abnormal hindbrain morphology">Abnormal hindbrain morphology</a></span><ul><li><span class="TLline"><a href="/medgen/869015" ref="tree=MeSH" title="MedGen record for Abnormal metencephalon morphology">Abnormal metencephalon morphology</a></span><ul><li><span class="TLline"><a href="/medgen/400925" ref="tree=MeSH" title="MedGen record for Abnormal cerebellum morphology">Abnormal cerebellum morphology</a></span><ul><li><span class="TLline"><a href="/medgen/196624" ref="tree=MeSH" title="MedGen record for Cerebellar atrophy">Cerebellar atrophy</a></span><ul><li><span class="matched_ds">Cerebellar cortical atrophy</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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<div class="portlet mgSection" id="ID_112">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln clinfeat">
<div class="divPopper rprt" id="rdis_6222"><div><strong>Marinesco-Sjögren syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>6222</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:">C0024814</span></a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Marinesco-Sjögren syndrome (MSS) is characterized by cerebellar ataxia with cerebellar atrophy, dysarthria, nystagmus, early-onset (not necessarily congenital) cataracts, myopathy, muscle weakness, and hypotonia. Additional features may include psychomotor delay, hypergonadotropic hypogonadism, short stature, and various skeletal abnormalities. Children with MSS usually present with muscular hypotonia in early infancy; distal and proximal muscular weakness is noticed during the first decade of life. Later, cerebellar findings of truncal ataxia, dysdiadochokinesia, nystagmus, and dysarthria become apparent. Motor function worsens progressively for some years, then stabilizes at an unpredictable age and degree of severity. Cataracts can develop rapidly and typically require lens extraction in the first decade of life. Although many adults have severe disabilities, life span in MSS appears to be near normal.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/6222">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_333031"><div><strong>CODAS syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>333031</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.">C1838180</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">CODAS is an acronym for cerebral, ocular, dental, auricular, and skeletal anomalies. CODAS syndrome is a rare disorder characterized by a distinctive constellation of features that includes developmental delay, craniofacial anomalies, cataracts, ptosis, median nasal groove, delayed tooth eruption, hearing loss, short stature, delayed epiphyseal ossification, metaphyseal hip dysplasia, and vertebral coronal clefts (summary by Strauss et al., 2015).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/333031">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_338301"><div><strong>Spinocerebellar ataxia type 15/16</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>338301</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.">C1847725</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Spinocerebellar ataxia-15 (SCA15) is an autosomal dominant, adult-onset, slowly progressive form of cerebellar ataxia. Most patients also have disabling action and postural tremor, and some have pyramidal tract affection, dorsal column involvement, and gaze palsy. Brain imaging shows cerebellar atrophy mainly affecting the vermis (summary by Synofzik et al., 2011).&#13; Autosomal dominant 'pure' cerebellar ataxia, classified as ADCA type III by Harding (1983, 1993), is a genetically heterogeneous disorder (see, e.g., 117210).&#13; For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/338301">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_338613"><div><strong>Infantile onset spinocerebellar ataxia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>338613</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.">C1849096</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Mitochondrial DNA depletion syndrome-7 is an autosomal recessive severe neurodegenerative disorder characterized primarily by hypotonia, ataxia, ophthalmoplegia, hearing loss, seizures, and sensory axonal neuropathy. Although originally classified as a form of spinocerebellar ataxia (see, e.g., SCA1, 164400) (Koskinen et al., 1994), it has been reclassified as a mitochondrial DNA depletion syndrome (Hakonen et al., 2008) based on the finding of mtDNA depletion in the brain and liver of affected individuals.&#13; For a discussion of genetic heterogeneity of autosomal recessive mtDNA depletion syndromes, see MTDPS1 (603041).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/338613">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1784590"><div><strong>Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1784590</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.">C5543375</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies (GKAF) is characterized by microcephaly, congenital alopecia, distinctive craniofacial features, severe congenital sensorineural hearing loss, global developmental delay, hydrocephalus, hypoplastic kidneys with renal insufficiency, genital hypoplasia, and early mortality (Ito et al., 2018).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1784590">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1858870"><div><strong>Developmental and epileptic encephalopathy 115</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1858870</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.">C5935604</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Developmental and epileptic encephalopathy-115 (DEE115) is an autosomal recessive disorder characterized by severe developmental delay and epileptic encephalopathy, massive reduction of white matter, hypo-/aplasia of the corpus callosum, neurodevelopmental arrest, and early death (Brugger et al., 2024).&#13; For general phenotypic information and a discussion of genetic heterogeneity of DEE, see 308350.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1858870">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1859522"><div><strong>Neurodevelopmental disorder plus optic atrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1859522</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.">C5935605</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Neurodevelopmental disorder plus optic atrophy (NEDOA) is an autosomal recessive disorder characterized by impaired intellectual development and childhood-onset optic atrophy or ataxia (Brugger et al., 2024).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1859522">Condition Record</a></div></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_333031" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">CODAS syndrome</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1858870" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental and epileptic encephalopathy 115</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1784590" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_338613" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Infantile onset spinocerebellar ataxia</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_6222" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Marinesco-Sjögren syndrome</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1859522" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder plus optic atrophy</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_338301" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 15/16</a></div></div>
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<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/29249373">Idiopathic cerebellar ataxia (IDCA): Diagnostic criteria and clinical analyses of 63 Japanese patients.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yoshida K,
Kuwabara S,
Nakamura K,
Abe R,
Matsushima A,
Beppu M,
Yamanaka Y,
Takahashi Y,
Sasaki H,
Mizusawa H;
Research Group on Ataxic Disorders</span><br />
<span class="medgenPMjournal">J Neurol Sci</span>
2018 Jan 15;384:30-35.
Epub 2017 Nov 7
doi: 10.1016/j.jns.2017.11.008.
<span class="bold">PMID: </span><a href="/pubmed/29249373" target="_blank">29249373</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26365142">GABAergic Pharmacotherapy in the Treatment of Motor Disorders of the Central Nervous System.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gazulla J,
Ruiz-Gazulla C,
Tintore M</span><br />
<span class="medgenPMjournal">Curr Pharm Des</span>
2015;21(34):4989-95.
doi: 10.2174/1381612821666150914120923.
<span class="bold">PMID: </span><a href="/pubmed/26365142" target="_blank">26365142</a></div>
<div class="nl"><a target="_blank" href="/pubmed/16147954">Treatment of cerebellar ataxia with 5-HT1A agonist.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Takei A,
Hamada T,
Yabe I,
Sasaki H</span><br />
<span class="medgenPMjournal">Cerebellum</span>
2005;4(3):211-5.
doi: 10.1080/14734220500222318.
<span class="bold">PMID: </span><a href="/pubmed/16147954" target="_blank">16147954</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22cerebellar%20cortical%20atrophy%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (3)</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/26856940">Longitudinal associations between brain structural changes and fatigue in early MS.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Nourbakhsh B,
Azevedo C,
Nunan-Saah J,
Maghzi AH,
Spain R,
Pelletier D,
Waubant E</span><br />
<span class="medgenPMjournal">Mult Scler Relat Disord</span>
2016 Jan;5:29-33.
Epub 2015 Oct 21
doi: 10.1016/j.msard.2015.10.006.
<span class="bold">PMID: </span><a href="/pubmed/26856940" target="_blank">26856940</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25150188">Comparisons of MR Findings Between Supratentorial and Infratentorial Gangliogliomas.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lou X,
Gui QP,
Sun L,
Wu NZ,
Lyu JH,
Ma L</span><br />
<span class="medgenPMjournal">Clin Neuroradiol</span>
2016 Mar;26(1):65-71.
Epub 2014 Aug 23
doi: 10.1007/s00062-014-0333-3.
<span class="bold">PMID: </span><a href="/pubmed/25150188" target="_blank">25150188</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26311179">Modulation of error-sensitivity during a prism adaptation task in people with cerebellar degeneration.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hanajima R,
Shadmehr R,
Ohminami S,
Tsutsumi R,
Shirota Y,
Shimizu T,
Tanaka N,
Terao Y,
Tsuji S,
Ugawa Y,
Uchimura M,
Inoue M,
Kitazawa S</span><br />
<span class="medgenPMjournal">J Neurophysiol</span>
2015 Oct;114(4):2460-71.
Epub 2015 Aug 26
doi: 10.1152/jn.00145.2015.
<span class="bold">PMID: </span><a href="/pubmed/26311179" target="_blank">26311179</a><a href="/pmc/articles/PMC4620141" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/22992533">Epilepsy in inherited metabolic disorders: a pediatric series.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vitiello G,
De Clemente V,
Della Casa R,
Romano A,
Rosa M,
Pascarella A,
Riccitelli M,
Parenti G,
Del Giudice E</span><br />
<span class="medgenPMjournal">Minerva Pediatr</span>
2012 Oct;64(5):513-20.
<span class="bold">PMID: </span><a href="/pubmed/22992533" target="_blank">22992533</a></div>
<div class="nl"><a target="_blank" href="/pubmed/8006682">Reduced cerebellar blood flow and oxygen metabolism in spinocerebellar degeneration: a combined PET and MRI study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Sun X,
Tanaka M,
Kondo S,
Hirai S,
Ishihara T</span><br />
<span class="medgenPMjournal">J Neurol</span>
1994 Mar;241(5):295-300.
doi: 10.1007/BF00868436.
<span class="bold">PMID: </span><a href="/pubmed/8006682" target="_blank">8006682</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%20cortical%20atrophy%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 (19)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/33581793">Hereditary spastic paraplegia type 11: Clinicogenetic lessons from 339 patients.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Du J</span><br />
<span class="medgenPMjournal">J Clin Neurosci</span>
2021 Mar;85:67-71.
Epub 2021 Jan 15
doi: 10.1016/j.jocn.2020.11.036.
<span class="bold">PMID: </span><a href="/pubmed/33581793" target="_blank">33581793</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25150188">Comparisons of MR Findings Between Supratentorial and Infratentorial Gangliogliomas.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lou X,
Gui QP,
Sun L,
Wu NZ,
Lyu JH,
Ma L</span><br />
<span class="medgenPMjournal">Clin Neuroradiol</span>
2016 Mar;26(1):65-71.
Epub 2014 Aug 23
doi: 10.1007/s00062-014-0333-3.
<span class="bold">PMID: </span><a href="/pubmed/25150188" target="_blank">25150188</a></div>
<div class="nl"><a target="_blank" href="/pubmed/17620549">Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">van der Knaap MS,
Linnankivi T,
Paetau A,
Feigenbaum A,
Wakusawa K,
Haginoya K,
Köhler W,
Henneke M,
Dinopoulos A,
Grattan-Smith P,
Brockmann K,
Schiffmann R,
Blaser S</span><br />
<span class="medgenPMjournal">Neurology</span>
2007 Jul 10;69(2):166-71.
doi: 10.1212/01.wnl.0000265592.74483.a6.
<span class="bold">PMID: </span><a href="/pubmed/17620549" target="_blank">17620549</a></div>
<div class="nl"><a target="_blank" href="/pubmed/12671958">High-dose piracetam is effective on cerebellar ataxia in patient with cerebellar cortical atrophy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vural M,
Ozekmekçi S,
Apaydin H,
Altinel A</span><br />
<span class="medgenPMjournal">Mov Disord</span>
2003 Apr;18(4):457-9.
doi: 10.1002/mds.10364.
<span class="bold">PMID: </span><a href="/pubmed/12671958" target="_blank">12671958</a></div>
<div class="nl"><a target="_blank" href="/pubmed/8334597">The cerebellar serotoninergic system and its possible involvement in cerebellar ataxia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Trouillas P</span><br />
<span class="medgenPMjournal">Can J Neurol Sci</span>
1993 May;20 Suppl 3:S78-82.
doi: 10.1017/s0317167100048575.
<span class="bold">PMID: </span><a href="/pubmed/8334597" target="_blank">8334597</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%20cortical%20atrophy%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 (31)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/26856940">Longitudinal associations between brain structural changes and fatigue in early MS.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Nourbakhsh B,
Azevedo C,
Nunan-Saah J,
Maghzi AH,
Spain R,
Pelletier D,
Waubant E</span><br />
<span class="medgenPMjournal">Mult Scler Relat Disord</span>
2016 Jan;5:29-33.
Epub 2015 Oct 21
doi: 10.1016/j.msard.2015.10.006.
<span class="bold">PMID: </span><a href="/pubmed/26856940" target="_blank">26856940</a></div>
<div class="nl"><a target="_blank" href="/pubmed/22992533">Epilepsy in inherited metabolic disorders: a pediatric series.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vitiello G,
De Clemente V,
Della Casa R,
Romano A,
Rosa M,
Pascarella A,
Riccitelli M,
Parenti G,
Del Giudice E</span><br />
<span class="medgenPMjournal">Minerva Pediatr</span>
2012 Oct;64(5):513-20.
<span class="bold">PMID: </span><a href="/pubmed/22992533" target="_blank">22992533</a></div>
<div class="nl"><a target="_blank" href="/pubmed/19443972">Intravenous immunoglobulin therapy for autoantibody-positive cerebellar ataxia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Nanri K,
Okita M,
Takeguchi M,
Taguchi T,
Ishiko T,
Saito H,
Otsuka T,
Mitoma H,
Koizumi K</span><br />
<span class="medgenPMjournal">Intern Med</span>
2009;48(10):783-90.
Epub 2009 May 15
doi: 10.2169/internalmedicine.48.1802.
<span class="bold">PMID: </span><a href="/pubmed/19443972" target="_blank">19443972</a></div>
<div class="nl"><a target="_blank" href="/pubmed/12671958">High-dose piracetam is effective on cerebellar ataxia in patient with cerebellar cortical atrophy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Vural M,
Ozekmekçi S,
Apaydin H,
Altinel A</span><br />
<span class="medgenPMjournal">Mov Disord</span>
2003 Apr;18(4):457-9.
doi: 10.1002/mds.10364.
<span class="bold">PMID: </span><a href="/pubmed/12671958" target="_blank">12671958</a></div>
<div class="nl"><a target="_blank" href="/pubmed/9193210">Buspirone, a 5-hydroxytryptamine1A agonist, is active in cerebellar ataxia. Results of a double-blind drug placebo study in patients with cerebellar cortical atrophy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Trouillas P,
Xie J,
Adeleine P,
Michel D,
Vighetto A,
Honnorat J,
Dumas R,
Nighoghossian N,
Laurent B</span><br />
<span class="medgenPMjournal">Arch Neurol</span>
1997 Jun;54(6):749-52.
doi: 10.1001/archneur.1997.00550180059013.
<span class="bold">PMID: </span><a href="/pubmed/9193210" target="_blank">9193210</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%20cortical%20atrophy%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 (14)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/33783722">A novel deletion variant in CLN3 with highly variable expressivity is responsible for juvenile neuronal ceroid lipofuscinoses.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gilani N,
Razmara E,
Ozaslan M,
Abdulzahra IK,
Arzhang S,
Tavasoli AR,
Garshasbi M</span><br />
<span class="medgenPMjournal">Acta Neurol Belg</span>
2021 Jun;121(3):737-748.
Epub 2021 Mar 30
doi: 10.1007/s13760-021-01655-9.
<span class="bold">PMID: </span><a href="/pubmed/33783722" target="_blank">33783722</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26856940">Longitudinal associations between brain structural changes and fatigue in early MS.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Nourbakhsh B,
Azevedo C,
Nunan-Saah J,
Maghzi AH,
Spain R,
Pelletier D,
Waubant E</span><br />
<span class="medgenPMjournal">Mult Scler Relat Disord</span>
2016 Jan;5:29-33.
Epub 2015 Oct 21
doi: 10.1016/j.msard.2015.10.006.
<span class="bold">PMID: </span><a href="/pubmed/26856940" target="_blank">26856940</a></div>
<div class="nl"><a target="_blank" href="/pubmed/17620549">Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">van der Knaap MS,
Linnankivi T,
Paetau A,
Feigenbaum A,
Wakusawa K,
Haginoya K,
Köhler W,
Henneke M,
Dinopoulos A,
Grattan-Smith P,
Brockmann K,
Schiffmann R,
Blaser S</span><br />
<span class="medgenPMjournal">Neurology</span>
2007 Jul 10;69(2):166-71.
doi: 10.1212/01.wnl.0000265592.74483.a6.
<span class="bold">PMID: </span><a href="/pubmed/17620549" target="_blank">17620549</a></div>
<div class="nl"><a target="_blank" href="/pubmed/10593305">Resetting of orthostatic tremor associated with cerebellar cortical atrophy by transcranial magnetic stimulation.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Manto MU,
Setta F,
Legros B,
Jacquy J,
Godaux E</span><br />
<span class="medgenPMjournal">Arch Neurol</span>
1999 Dec;56(12):1497-500.
doi: 10.1001/archneur.56.12.1497.
<span class="bold">PMID: </span><a href="/pubmed/10593305" target="_blank">10593305</a></div>
<div class="nl"><a target="_blank" href="/pubmed/1171401">"Saccadic nystagmus" in cerebellar cortical atrophy.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Alpert JN,
Coats AC,
Perusquia E</span><br />
<span class="medgenPMjournal">Neurology</span>
1975 Jul;25(7):676-80.
doi: 10.1212/wnl.25.7.676.
<span class="bold">PMID: </span><a href="/pubmed/1171401" target="_blank">1171401</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%20cortical%20atrophy%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 (16)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/33581793">Hereditary spastic paraplegia type 11: Clinicogenetic lessons from 339 patients.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Du J</span><br />
<span class="medgenPMjournal">J Clin Neurosci</span>
2021 Mar;85:67-71.
Epub 2021 Jan 15
doi: 10.1016/j.jocn.2020.11.036.
<span class="bold">PMID: </span><a href="/pubmed/33581793" target="_blank">33581793</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30630042">Resistance, vulnerability and resilience: A review of the cognitive cerebellum in aging and neurodegenerative diseases.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Liang KJ,
Carlson ES</span><br />
<span class="medgenPMjournal">Neurobiol Learn Mem</span>
2020 Apr;170:106981.
Epub 2019 Jan 7
doi: 10.1016/j.nlm.2019.01.004.
<span class="bold">PMID: </span><a href="/pubmed/30630042" target="_blank">30630042</a><a href="/pmc/articles/PMC6612482" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/25150188">Comparisons of MR Findings Between Supratentorial and Infratentorial Gangliogliomas.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lou X,
Gui QP,
Sun L,
Wu NZ,
Lyu JH,
Ma L</span><br />
<span class="medgenPMjournal">Clin Neuroradiol</span>
2016 Mar;26(1):65-71.
Epub 2014 Aug 23
doi: 10.1007/s00062-014-0333-3.
<span class="bold">PMID: </span><a href="/pubmed/25150188" target="_blank">25150188</a></div>
<div class="nl"><a target="_blank" href="/pubmed/17620549">Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">van der Knaap MS,
Linnankivi T,
Paetau A,
Feigenbaum A,
Wakusawa K,
Haginoya K,
Köhler W,
Henneke M,
Dinopoulos A,
Grattan-Smith P,
Brockmann K,
Schiffmann R,
Blaser S</span><br />
<span class="medgenPMjournal">Neurology</span>
2007 Jul 10;69(2):166-71.
doi: 10.1212/01.wnl.0000265592.74483.a6.
<span class="bold">PMID: </span><a href="/pubmed/17620549" target="_blank">17620549</a></div>
<div class="nl"><a target="_blank" href="/pubmed/8334597">The cerebellar serotoninergic system and its possible involvement in cerebellar ataxia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Trouillas P</span><br />
<span class="medgenPMjournal">Can J Neurol Sci</span>
1993 May;20 Suppl 3:S78-82.
doi: 10.1017/s0317167100048575.
<span class="bold">PMID: </span><a href="/pubmed/8334597" target="_blank">8334597</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%20cortical%20atrophy%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 (25)</a></div></div>
</div>
<div class="portlet mgSection" id="ID_104">
<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/33581793">Hereditary spastic paraplegia type 11: Clinicogenetic lessons from 339 patients.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Du J</span><br />
<span class="medgenPMjournal">J Clin Neurosci</span>
2021 Mar;85:67-71.
Epub 2021 Jan 15
doi: 10.1016/j.jocn.2020.11.036.
<span class="bold">PMID: </span><a href="/pubmed/33581793" target="_blank">33581793</a></div>
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