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<!--
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UID=375309
|
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ConceptID=C1843885
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Progressive gait ataxia</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>375309</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.">C1843885</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Gait ataxia, progressive</td></tr>
|
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<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0007240">HP:0007240</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">A type of gait ataxia displaying progression of clinical severity. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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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">Progressive gait ataxia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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="TLline"><a href="/medgen/868940" ref="tree=MeSH" title="MedGen record for Abnormal central motor function">Abnormal central motor function</a></span><ul><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/13945" ref="tree=MeSH" title="MedGen record for Dyssynergia">Dyssynergia</a></span><ul><li><span class="TLline"><a href="/medgen/155642" ref="tree=MeSH" title="MedGen record for Gait ataxia">Gait ataxia</a></span><ul><li><span class="matched_ds">Progressive gait ataxia</span></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_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_58144"><div><strong>Angelman syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>58144</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.">C0162635</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Angelman syndrome (AS) is characterized by severe developmental delay or intellectual disability, severe speech impairment, gait ataxia and/or tremulousness of the limbs, and unique behavior with an apparent happy demeanor that includes frequent laughing, smiling, and excitability. Microcephaly and seizures are also common. Developmental delays are first noted at around age six months; however, the unique clinical features of AS do not become manifest until after age one year.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/58144">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_375302"><div><strong>Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>375302</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.">C1843851</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">POLG-related disorders comprise a continuum of overlapping phenotypes that were clinically defined before the molecular basis was known. POLG-related disorders can therefore be considered an overlapping spectrum of disease presenting from early childhood to late adulthood. The age of onset broadly correlates with the clinical phenotype. In individuals with early-onset disease (prior to age 12 years), liver involvement, feeding difficulties, seizures, hypotonia, and muscle weakness are the most common clinical features. This group has the worst prognosis. In the juvenile/adult-onset form (age 12-40 years), disease is typically characterized by peripheral neuropathy, ataxia, seizures, stroke-like episodes, and, in individuals with longer survival, progressive external ophthalmoplegia (PEO). This group generally has a better prognosis than the early-onset group. Late-onset disease (after age 40 years) is characterized by ptosis and PEO, with additional features such as peripheral neuropathy, ataxia, and muscle weakness. This group overall has the best prognosis.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/375302">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_336066"><div><strong>Spinocerebellar ataxia type 18</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>336066</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.">C1843884</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Disease with characteristics of sensory neuropathy and cerebellar ataxia. Prevalence is unknown. Only 26 cases in a 5-generation American family of Irish ancestry have been reported to date. Onset is in the second and third decades of life with symptomatic onset ranging from 13 to 27 years. Patients initially present with axonal sensory neuropathy, while cerebellar ataxia and motor neuron dysfunction develop later. Linked to chromosome 7q22-q23 but the responsible gene mutation has not yet been identified.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/336066">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_338620"><div><strong>Charlevoix-Saguenay spastic ataxia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>338620</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C1849140</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is clinically characterized by a progressive cerebellar ataxia, peripheral neuropathy, and spasticity. Disease onset of classic ARSACS is often in early childhood, leading to delayed walking because of gait unsteadiness in very young toddlers, while an increasing number of individuals with disease onset in teenage or early-adult years are now being described. Typically the ataxia is followed by lower-limb spasticity and later by peripheral neuropathy – although pronounced peripheral neuropathy has been observed as a first sign of ARSACS. Oculomotor disturbances, dysarthria, and upper-limb ataxia develop with slower progression than the other findings. Brain imaging demonstrates atrophy of the superior vermis and the cerebellar hemisphere with additional findings on MRI, such as linear hypointensities in the pons and hyperintense rims around the thalami. Many affected individuals (though not all) have yellow streaks of hypermyelinated fibers radiating from the edges of the optic disc noted on ophthalmologic exam, and thickened retinal fibers can be demonstrated by optical coherence tomography. Mild intellectual disability, hearing loss, and urinary urgency and incontinence have been reported in some individuals.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/338620">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_340052"><div><strong>Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>340052</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.">C1853761</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Ataxia with oculomotor apraxia type 2 (AOA2) is characterized by onset of ataxia between age three and 30 years after initial normal development, axonal sensorimotor neuropathy, oculomotor apraxia, cerebellar atrophy, and elevated serum concentration of alpha-fetoprotein (AFP).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/340052">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_58144" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Angelman syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_338620" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Charlevoix-Saguenay spastic ataxia</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_375302" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_336066" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 18</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_340052" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37691319">Propensity matched comparison of omaveloxolone treatment to Friedreich ataxia natural history data.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lynch DR,
|
||
Goldsberry A,
|
||
Rummey C,
|
||
Farmer J,
|
||
Boesch S,
|
||
Delatycki MB,
|
||
Giunti P,
|
||
Hoyle JC,
|
||
Mariotti C,
|
||
Mathews KD,
|
||
Nachbauer W,
|
||
Perlman S,
|
||
Subramony SH,
|
||
Wilmot G,
|
||
Zesiewicz T,
|
||
Weissfeld L,
|
||
Meyer C</span><br />
|
||
<span class="medgenPMjournal">Ann Clin Transl Neurol</span>
|
||
2024 Jan;11(1):4-16.
|
||
Epub 2023 Sep 10
|
||
doi: 10.1002/acn3.51897.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37691319" target="_blank">37691319</a><a href="/pmc/articles/PMC10791025" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37090712">Rehabilitation treatment of multiple sclerosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Duan H,
|
||
Jing Y,
|
||
Li Y,
|
||
Lian Y,
|
||
Li J,
|
||
Li Z</span><br />
|
||
<span class="medgenPMjournal">Front Immunol</span>
|
||
2023;14:1168821.
|
||
Epub 2023 Apr 6
|
||
doi: 10.3389/fimmu.2023.1168821.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37090712" target="_blank">37090712</a><a href="/pmc/articles/PMC10117641" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31887755">Cerebellar Dizziness and Vertigo: Etiologies, Diagnostic Assessment, and Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zwergal A,
|
||
Feil K,
|
||
Schniepp R,
|
||
Strupp M</span><br />
|
||
<span class="medgenPMjournal">Semin Neurol</span>
|
||
2020 Feb;40(1):87-96.
|
||
Epub 2019 Dec 30
|
||
doi: 10.1055/s-0039-3400315.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31887755" target="_blank">31887755</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(progressive%20gait%20ataxia)%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 (21)</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/39867503">Ocular Telangiectasia and Cerebellar Atrophy in Ataxia-Telangiectasia (Louis-Bar Syndrome).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gattermeyer-Kell L,
|
||
Kern D,
|
||
Kögl M,
|
||
Schwingenschuh P</span><br />
|
||
<span class="medgenPMjournal">Tremor Other Hyperkinet Mov (N Y)</span>
|
||
2025;15:4.
|
||
Epub 2025 Jan 20
|
||
doi: 10.5334/tohm.992.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39867503" target="_blank">39867503</a><a href="/pmc/articles/PMC11758811" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37101238">Spinocerebellar ataxia type 14 (SCA14) in an Argentinian family: a case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Duggirala N,
|
||
Ngo KJ,
|
||
Pagnoni SM,
|
||
Rosa AL,
|
||
Fogel BL</span><br />
|
||
<span class="medgenPMjournal">J Med Case Rep</span>
|
||
2023 Apr 27;17(1):168.
|
||
doi: 10.1186/s13256-023-03897-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37101238" target="_blank">37101238</a><a href="/pmc/articles/PMC10134643" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27658421">Progressive gait ataxia following deep brain stimulation for essential tremor: adverse effect or lack of efficacy?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Reich MM,
|
||
Brumberg J,
|
||
Pozzi NG,
|
||
Marotta G,
|
||
Roothans J,
|
||
Åström M,
|
||
Musacchio T,
|
||
Lopiano L,
|
||
Lanotte M,
|
||
Lehrke R,
|
||
Buck AK,
|
||
Volkmann J,
|
||
Isaias IU</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2016 Nov 1;139(11):2948-2956.
|
||
doi: 10.1093/brain/aww223.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27658421" target="_blank">27658421</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25085749">Identification of FXTAS presenting with SCA 12 like phenotype in India.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Faruq M,
|
||
Srivastava AK,
|
||
Suroliya V,
|
||
Kumar D,
|
||
Garg A,
|
||
Shukla G,
|
||
Behari M</span><br />
|
||
<span class="medgenPMjournal">Parkinsonism Relat Disord</span>
|
||
2014 Oct;20(10):1089-93.
|
||
Epub 2014 Jul 17
|
||
doi: 10.1016/j.parkreldis.2014.07.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25085749" target="_blank">25085749</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15732118">Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yu GY,
|
||
Howell MJ,
|
||
Roller MJ,
|
||
Xie TD,
|
||
Gomez CM</span><br />
|
||
<span class="medgenPMjournal">Ann Neurol</span>
|
||
2005 Mar;57(3):349-54.
|
||
doi: 10.1002/ana.20371.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15732118" target="_blank">15732118</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Progressive%20gait%20ataxia%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 (8)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30783548">Arm Levitation as Initial Manifestation of Creutzfeldt-Jakob Disease: Case Report and Review of the Literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ciarlariello VB,
|
||
Barsottini OGP,
|
||
Espay AJ,
|
||
Pedroso JL</span><br />
|
||
<span class="medgenPMjournal">Tremor Other Hyperkinet Mov (N Y)</span>
|
||
2018;8:572.
|
||
Epub 2018 Dec 10
|
||
doi: 10.7916/D80C6CGX.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30783548" target="_blank">30783548</a><a href="/pmc/articles/PMC6377915" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29530967">Clinical Reasoning: A 52-year-old woman with 3 weeks of progressive gait ataxia and dysarthria.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lu C,
|
||
Velickovic Ostojic L,
|
||
Lemus HN</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2018 Mar 13;90(11):e985-e989.
|
||
doi: 10.1212/WNL.0000000000005122.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29530967" target="_blank">29530967</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28437518">A Middle-aged Man With Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kung NH,
|
||
Van Stavern GP,
|
||
Bucelli RC</span><br />
|
||
<span class="medgenPMjournal">JAMA Neurol</span>
|
||
2017 Jun 1;74(6):733-736.
|
||
doi: 10.1001/jamaneurol.2017.0055.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28437518" target="_blank">28437518</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28226077">Superficial siderosis of the central nervous system is a rare and possibly underdiagnosed disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fragoso YD,
|
||
Adoni T,
|
||
Brooks JB,
|
||
Gomes S,
|
||
Goncalves MV,
|
||
Jovem CL,
|
||
Matta AP,
|
||
Oliveira JF,
|
||
Siquinelli F,
|
||
Tauil CB,
|
||
Troiani GN,
|
||
Wille PR</span><br />
|
||
<span class="medgenPMjournal">Arq Neuropsiquiatr</span>
|
||
2017 Feb;75(2):92-95.
|
||
doi: 10.1590/0004-282X20170001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28226077" target="_blank">28226077</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27143115">Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Borroni B,
|
||
Di Gregorio E,
|
||
Orsi L,
|
||
Vaula G,
|
||
Costanzi C,
|
||
Tempia F,
|
||
Mitro N,
|
||
Caruso D,
|
||
Manes M,
|
||
Pinessi L,
|
||
Padovani A,
|
||
Brusco A,
|
||
Boccone L</span><br />
|
||
<span class="medgenPMjournal">Parkinsonism Relat Disord</span>
|
||
2016 Jul;28:80-6.
|
||
Epub 2016 Apr 27
|
||
doi: 10.1016/j.parkreldis.2016.04.030.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27143115" target="_blank">27143115</a><a href="/pmc/articles/PMC4925464" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Progressive%20gait%20ataxia%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 (34)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38484218">Immune Checkpoint Inhibitor-Associated Kelch-Like Protein-11 IgG Brainstem Encephalitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aboseif A,
|
||
Vorasoot N,
|
||
Pinto MV,
|
||
Guo Y,
|
||
Hasan S,
|
||
Zekeridou A,
|
||
Chen JJ,
|
||
Dubey D</span><br />
|
||
<span class="medgenPMjournal">Neurol Neuroimmunol Neuroinflamm</span>
|
||
2024 May;11(3):e200218.
|
||
Epub 2024 Mar 14
|
||
doi: 10.1212/NXI.0000000000200218.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38484218" target="_blank">38484218</a><a href="/pmc/articles/PMC11073878" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36717159">Varicella zoster virus cerebellitis without skin manifestations in an immunocompetent adult.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Enwo OO,
|
||
Ibrahim D,
|
||
Boughton M,
|
||
Coyle-Gilchrist I</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2023 Jan 30;16(1)
|
||
doi: 10.1136/bcr-2022-252636.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36717159" target="_blank">36717159</a><a href="/pmc/articles/PMC9887685" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27658421">Progressive gait ataxia following deep brain stimulation for essential tremor: adverse effect or lack of efficacy?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Reich MM,
|
||
Brumberg J,
|
||
Pozzi NG,
|
||
Marotta G,
|
||
Roothans J,
|
||
Åström M,
|
||
Musacchio T,
|
||
Lopiano L,
|
||
Lanotte M,
|
||
Lehrke R,
|
||
Buck AK,
|
||
Volkmann J,
|
||
Isaias IU</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2016 Nov 1;139(11):2948-2956.
|
||
doi: 10.1093/brain/aww223.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27658421" target="_blank">27658421</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26243623">Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) after treatment for Hodgkin's lymphoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mashima K,
|
||
Suzuki S,
|
||
Mori T,
|
||
Shimizu T,
|
||
Yamada S,
|
||
Hirose S,
|
||
Okamoto S,
|
||
Suzuki N</span><br />
|
||
<span class="medgenPMjournal">Int J Hematol</span>
|
||
2015 Dec;102(6):709-12.
|
||
Epub 2015 Aug 5
|
||
doi: 10.1007/s12185-015-1850-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26243623" target="_blank">26243623</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24019389">Clinical reasoning: a 48-year-old woman with progressive spastic-ataxic gait.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kerasnoudis A,
|
||
Décard BF,
|
||
Gold R</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2013 Sep 10;81(11):e75-80.
|
||
doi: 10.1212/WNL.0b013e3182a43ad9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24019389" target="_blank">24019389</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Progressive%20gait%20ataxia%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/37154409">Spinocerebellar ataxia type 15 caused by missense variants in the ITPR1 gene.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gazulla J,
|
||
Bellosta-Diago E,
|
||
Izquierdo-Alvarez S,
|
||
Berciano J</span><br />
|
||
<span class="medgenPMjournal">Eur J Neurol</span>
|
||
2023 Aug;30(8):2539-2543.
|
||
Epub 2023 May 19
|
||
doi: 10.1111/ene.15840.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37154409" target="_blank">37154409</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26252983">CLIPPERS Syndrome: An Entity to be Faced in Neurosurgery.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Esmaeilzadeh M,
|
||
Yildiz Ö,
|
||
Lang JM,
|
||
Wegner F,
|
||
Haubitz B,
|
||
Feuerhake F,
|
||
Wrede A,
|
||
Brück W,
|
||
Dengler R,
|
||
Krauss JK</span><br />
|
||
<span class="medgenPMjournal">World Neurosurg</span>
|
||
2015 Dec;84(6):2077.e1-3.
|
||
Epub 2015 Aug 4
|
||
doi: 10.1016/j.wneu.2015.07.057.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26252983" target="_blank">26252983</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23996585">Quantitative profiling and identification of differentially expressed plasma proteins in Friedreich's ataxia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Swarup V,
|
||
Srivastava AK,
|
||
Padma MV,
|
||
Rajeswari MR</span><br />
|
||
<span class="medgenPMjournal">J Neurosci Res</span>
|
||
2013 Nov;91(11):1483-91.
|
||
Epub 2013 Aug 30
|
||
doi: 10.1002/jnr.23262.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23996585" target="_blank">23996585</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15732118">Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yu GY,
|
||
Howell MJ,
|
||
Roller MJ,
|
||
Xie TD,
|
||
Gomez CM</span><br />
|
||
<span class="medgenPMjournal">Ann Neurol</span>
|
||
2005 Mar;57(3):349-54.
|
||
doi: 10.1002/ana.20371.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15732118" target="_blank">15732118</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7990851">Superficial hemosiderosis of the central nervous system.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">River Y,
|
||
Honigman S,
|
||
Gomori JM,
|
||
Reches A</span><br />
|
||
<span class="medgenPMjournal">Mov Disord</span>
|
||
1994 Sep;9(5):559-62.
|
||
doi: 10.1002/mds.870090509.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7990851" target="_blank">7990851</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Progressive%20gait%20ataxia%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 (8)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37154409">Spinocerebellar ataxia type 15 caused by missense variants in the ITPR1 gene.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gazulla J,
|
||
Bellosta-Diago E,
|
||
Izquierdo-Alvarez S,
|
||
Berciano J</span><br />
|
||
<span class="medgenPMjournal">Eur J Neurol</span>
|
||
2023 Aug;30(8):2539-2543.
|
||
Epub 2023 May 19
|
||
doi: 10.1111/ene.15840.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37154409" target="_blank">37154409</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32471306">Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Stendel C,
|
||
D'Adamo MC,
|
||
Wiessner M,
|
||
Dusl M,
|
||
Cenciarini M,
|
||
Belia S,
|
||
Nematian-Ardestani E,
|
||
Bauer P,
|
||
Senderek J,
|
||
Klopstock T,
|
||
Pessia M</span><br />
|
||
<span class="medgenPMjournal">Int J Mol Sci</span>
|
||
2020 May 27;21(11)
|
||
doi: 10.3390/ijms21113810.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32471306" target="_blank">32471306</a><a href="/pmc/articles/PMC7312673" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28437518">A Middle-aged Man With Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kung NH,
|
||
Van Stavern GP,
|
||
Bucelli RC</span><br />
|
||
<span class="medgenPMjournal">JAMA Neurol</span>
|
||
2017 Jun 1;74(6):733-736.
|
||
doi: 10.1001/jamaneurol.2017.0055.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28437518" target="_blank">28437518</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23996585">Quantitative profiling and identification of differentially expressed plasma proteins in Friedreich's ataxia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Swarup V,
|
||
Srivastava AK,
|
||
Padma MV,
|
||
Rajeswari MR</span><br />
|
||
<span class="medgenPMjournal">J Neurosci Res</span>
|
||
2013 Nov;91(11):1483-91.
|
||
Epub 2013 Aug 30
|
||
doi: 10.1002/jnr.23262.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23996585" target="_blank">23996585</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15732118">Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yu GY,
|
||
Howell MJ,
|
||
Roller MJ,
|
||
Xie TD,
|
||
Gomez CM</span><br />
|
||
<span class="medgenPMjournal">Ann Neurol</span>
|
||
2005 Mar;57(3):349-54.
|
||
doi: 10.1002/ana.20371.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15732118" target="_blank">15732118</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Progressive%20gait%20ataxia%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 (10)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
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<div class="portlet mgSection" id="ID_113">
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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_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Progressive%20gait%20ataxia" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_121">
|
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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>
|
||
<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(progressive%20gait%20ataxia)%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(%22Progressive%20gait%20ataxia%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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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Progressive%20gait%20ataxia" target="_blank">MedlinePlus</a></li></ul></div>
|
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenReviews.Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="Reviews" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenReviews.Shutter"></a>
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<li>
|
||
<a href="/pubmed/clinical?term=Progressive%20gait%20ataxia" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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|
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<a href="/pubmed?term=Progressive%20gait%20ataxia%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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<h3>Related information</h3>
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<div class="portlet_content DiscoveryDbLinks">
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<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=375309" ref="log$=recordlinks">ClinVar</a>
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<div class="brieflinkpop offscreen_noflow">Related medical variations</div>
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=375309" ref="log$=recordlinks">PMC Articles</a>
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=375309" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="recent_activity" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.Shutter"></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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Clear
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||
</a>
|
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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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Turn Off
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</a>
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" sid="2" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" class="HTOff" cmd="HTOn" href="?cmd=HTOn&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle">
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Turn On
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|
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|
||
<ul id="activity">
|
||
<li class="ra_rcd ralinkpopper two_line">
|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d2c9f82f30673f7bb8e586">Progressive gait ataxia</a>
|
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<div class="ralinkpop offscreen_noflow">Progressive gait ataxia<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary">MedGen</div>
|
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</li>
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<li class="ra_rcd ralinkpopper two_line">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d2c9f52f30673f7bb8d45d">Upper motor neuron dysfunction</a>
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<div class="ralinkpop offscreen_noflow">Upper motor neuron dysfunction<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
|
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</li>
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||
<li class="ra_rcd ralinkpopper two_line">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d2c9f467c23b31e088ba52">Cerebellar vermis atrophy</a>
|
||
<div class="ralinkpop offscreen_noflow">Cerebellar vermis atrophy<div class="brieflinkpopdesc"></div></div>
|
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<div class="tertiary">MedGen</div>
|
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</li>
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<li class="ra_rcd ralinkpopper two_line">
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=4" href="/portal/utils/pageresolver.fcgi?recordid=67d2c9f12f30673f7bb8b839">Scanning speech</a>
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