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<!--
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UID=140835
|
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ConceptID=C0423083
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Hypermetric saccades</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>140835</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.">C0423083</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Hypermetric saccades (246769000)</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:0007338">HP:0007338</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 saccade that overshoots the target with the dynamic saccade. [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>
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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="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Hypermetric saccades</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/1370071" ref="tree=MeSH" title="MedGen record for Abnormality of the eye">Abnormality of the eye</a></span><ul><li><span class="TLline"><a href="/medgen/868525" ref="tree=MeSH" title="MedGen record for Abnormal eye physiology">Abnormal eye physiology</a></span><ul><li><span class="TLline"><a href="/medgen/99227" ref="tree=MeSH" title="MedGen record for Abnormality of eye movement">Abnormality of eye movement</a></span><ul><li><span class="TLline"><a href="/medgen/66709" ref="tree=MeSH" title="MedGen record for Abnormal saccadic eye movements">Abnormal saccadic eye movements</a></span><ul><li><span class="matched_ds">Hypermetric saccades</span><ul><li><span class="TLline"><a href="/medgen/1635433" ref="tree=MeSH" title="MedGen record for Hypermetric downward saccades">Hypermetric downward saccades</a></span></li><li><span class="TLline"><a href="/medgen/1671023" ref="tree=MeSH" title="MedGen record for Hypermetric horizontal saccades">Hypermetric horizontal saccades</a></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">
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||
<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>
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<div class="portlet_content ln clinfeat">
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||
<div class="divPopper rprt" id="rdis_324520"><div><strong>Autosomal recessive spinocerebellar ataxia 7</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>324520</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.">C1836474</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spinocerebellar ataxia is a neurologic disorder characterized by onset of progressive gait difficulties, eye movement abnormalities, and dysarthria in the first or second decade of life (summary by Dy et al., 2015).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/324520">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_373352"><div><strong>Spinocerebellar ataxia type 20</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>373352</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.">C1837541</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spinocerebellar ataxia type 20 (SCA20) is characterized by a slowly progressive ataxia and dysarthria. Approximately two thirds of those affected also display palatal tremor ("myoclonus") and/or abnormal phonation clinically resembling spasmodic adductor dysphonia. Dysarthria, which may be abrupt in onset, precedes the onset of ataxia in about two thirds of affected individuals, sometimes by a number of years. Hypermetric horizontal saccades (without nystagmus or disturbance of vestibulo-ocular reflex gain) are seen in about half of affected persons. Although minor pyramidal signs (brisk knee jerks, crossed adductor spread) may be seen, spasticity and extensor plantar responses are not. Cognition is normal. Clinical information is based on the findings in 16 personally examined affected members of a single Australian family of Anglo-Celtic descent.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/373352">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_375311"><div><strong>Spinocerebellar ataxia type 21</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>375311</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.">C1843891</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spinocerebellar ataxia-21 (SCA21) is an autosomal dominant neurologic disorder characterized by onset in the first decades of life of slowly progressive cerebellar ataxia, which is associated with cognitive impairment in most patients (summary by Delplanque et al., 2014). For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/375311">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_335442"><div><strong>Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>335442</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.">C1846492</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">VPS13D movement disorder is a hyperkinetic movement disorder (dystonia, chorea, and/or ataxia) of variable age of onset that can be associated with developmental delay. Onset ranges from birth to adulthood. Individuals can present in childhood with motor delays and gait instability. Cognitive impairment ranging from mild intellectual disability to developmental delay has been reported, and several individuals have normal cognitive function. Individuals have also presented as young adults with gait difficulties caused by spastic ataxia or ataxia. In addition to gait ataxia, affected individuals had limb ataxia, dysarthria, and eye movement abnormalities (macro-saccadic oscillations, nystagmus, and saccadic pursuit). Additional features reported in some individuals include peripheral neuropathy and/or seizures. The disorder progresses to spastic ataxia or generalized dystonia, which can lead to loss of independent ambulation.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/335442">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) 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). Autosomal dominant 'pure' cerebellar ataxia, classified as ADCA type III by Harding (1983, 1993), is a genetically heterogeneous disorder (see, e.g., 117210). 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_424821"><div><strong>Spinocerebellar ataxia type 30</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>424821</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.">C2936793</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare disease with characteristics of slowly progressive and relatively pure ataxia described in 6 patients from one Australian family to date. The disease presents with oculomotor dysfunction, moderate dysarthria, and ataxia that progresses slowly and eventually leads to mobility impairment. Some patients have also reported mild hyperreflexia in the lower limbs. Rare manifestations include gaze-evoked nystagmus and dystonia. The causal gene has not yet been identified but it has been linked to chromosome 4q34.3-q35.1.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/424821">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_462348"><div><strong>Autosomal recessive spinocerebellar ataxia 10</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>462348</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.">C3150998</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spinocerebellar ataxia-10 is an autosomal recessive neurodegenerative disorder with onset in the teenage or young adult years of gait and limb ataxia, dysarthria, and nystagmus associated with marked cerebellar atrophy on brain imaging (summary by Vermeer et al., 2010). Some patients have low levels of coenzyme Q10 (CoQ10) in muscle and may show some clinical improvement with CoQ10 treatment (Balreira et al., 2014).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/462348">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1611168"><div><strong>Spinocerebellar ataxia 44</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1611168</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.">C4521563</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1611168">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1617917"><div><strong>Spinocerebellar ataxia, autosomal recessive 26</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1617917</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.">C4539948</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1617917">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1672866"><div><strong>Spinocerebellar ataxia, autosomal recessive 27</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1672866</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.">C5193058</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spinocerebellar ataxia-27 (SCAR27) is an adult-onset neurologic disorder characterized by gait difficulties and other cerebellar signs, such as eye movement abnormalities, dysarthria, and difficulty writing. The disorder is progressive, and some patients may lose independent ambulation. Additional features include spasticity of the lower limbs and cognitive impairment. Brain imaging shows cerebellar atrophy (summary by Eidhof et al., 2018).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1672866">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1805016"><div><strong>Dystonia 34, myoclonic</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1805016</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.">C5676907</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Myoclonic dystonia-34 (DYT34) is an autosomal dominant neurologic disorder characterized by childhood-onset dystonia primarily involving the hands and neck, with a fast tremor with superimposed myoclonus (Balint et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1805016">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1802496"><div><strong>Spinocerebellar ataxia, autosomal recessive 32</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1802496</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.">C5676978</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spinocerebellar ataxia-32 (SCAR32) is a neurologic disorder characterized by the onset of gait ataxia in the second or third decades of life. The disorder is slowly progressive. Other classic features include upper limb ataxia, oculomotor signs, dysphagia, and dysarthria. Some patients may have hyper- or hypokinetic movement abnormalities. Brain imaging shows cerebellar atrophy (Rebelo et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1802496">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_335442" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_462348" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive spinocerebellar ataxia 10</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_324520" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive spinocerebellar ataxia 7</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1805016" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Dystonia 34, myoclonic</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1611168" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia 44</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (12)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<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 class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_373352" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 20</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_375311" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 21</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_424821" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 30</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1617917" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia, autosomal recessive 26</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1672866" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia, autosomal recessive 27</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1802496" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia, autosomal recessive 32</a></div></span></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/37000368">Oculomotor Impairments in Children After Posterior Fossa Tumors Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shurupova MA,
|
||
Latanov AV</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2024 Apr;23(2):444-454.
|
||
Epub 2023 Mar 31
|
||
doi: 10.1007/s12311-023-01553-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37000368" target="_blank">37000368</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22hypermetric%20saccades%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (1)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35760933">Eye movement abnormalities in neurodegenerative langerhans cell histiocytosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Autier L,
|
||
Gaymard B,
|
||
Bayen E,
|
||
Del Cul A,
|
||
Cohen-Aubart F,
|
||
Martin-Duverneuil N,
|
||
Haroche J,
|
||
Mokhtari K,
|
||
Héritier S,
|
||
Donadieu J,
|
||
Hoang-Xuan K,
|
||
Idbaih A</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2022 Nov;43(11):6539-6546.
|
||
Epub 2022 Jun 28
|
||
doi: 10.1007/s10072-022-06180-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35760933" target="_blank">35760933</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28688606">A clinical and neurophysiological motor signature of Unverricht-Lundborg disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hainque E,
|
||
Blancher A,
|
||
Mesnage V,
|
||
Rivaud-Pechoux S,
|
||
Bertrand A,
|
||
Dupont S,
|
||
Navarro V,
|
||
Roze E,
|
||
Gourfinkel-An I,
|
||
Apartis E</span><br />
|
||
<span class="medgenPMjournal">Rev Neurol (Paris)</span>
|
||
2018 Jan-Feb;174(1-2):56-65.
|
||
Epub 2017 Jul 5
|
||
doi: 10.1016/j.neurol.2017.06.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28688606" target="_blank">28688606</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15855027">Audio-vestibular disturbances in Behcet's patients: report of 62 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kulahli I,
|
||
Balci K,
|
||
Koseoglu E,
|
||
Yuce I,
|
||
Cagli S,
|
||
Senturk M</span><br />
|
||
<span class="medgenPMjournal">Hear Res</span>
|
||
2005 May;203(1-2):28-31.
|
||
doi: 10.1016/j.heares.2004.11.020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15855027" target="_blank">15855027</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14998916">Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Knight MA,
|
||
Gardner RJ,
|
||
Bahlo M,
|
||
Matsuura T,
|
||
Dixon JA,
|
||
Forrest SM,
|
||
Storey E</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2004 May;127(Pt 5):1172-81.
|
||
Epub 2004 Mar 3
|
||
doi: 10.1093/brain/awh139.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14998916" target="_blank">14998916</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14725795">Saccade dysmetria in Williams-Beuren syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van der Geest JN,
|
||
Lagers-van Haselen GC,
|
||
van Hagen JM,
|
||
Govaerts LC,
|
||
de Coo IF,
|
||
de Zeeuw CI,
|
||
Frens MA</span><br />
|
||
<span class="medgenPMjournal">Neuropsychologia</span>
|
||
2004;42(5):569-76.
|
||
doi: 10.1016/j.neuropsychologia.2003.11.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14725795" target="_blank">14725795</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypermetric%20saccades%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 (7)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37000368">Oculomotor Impairments in Children After Posterior Fossa Tumors Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shurupova MA,
|
||
Latanov AV</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2024 Apr;23(2):444-454.
|
||
Epub 2023 Mar 31
|
||
doi: 10.1007/s12311-023-01553-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37000368" target="_blank">37000368</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35760933">Eye movement abnormalities in neurodegenerative langerhans cell histiocytosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Autier L,
|
||
Gaymard B,
|
||
Bayen E,
|
||
Del Cul A,
|
||
Cohen-Aubart F,
|
||
Martin-Duverneuil N,
|
||
Haroche J,
|
||
Mokhtari K,
|
||
Héritier S,
|
||
Donadieu J,
|
||
Hoang-Xuan K,
|
||
Idbaih A</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2022 Nov;43(11):6539-6546.
|
||
Epub 2022 Jun 28
|
||
doi: 10.1007/s10072-022-06180-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35760933" target="_blank">35760933</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28688606">A clinical and neurophysiological motor signature of Unverricht-Lundborg disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hainque E,
|
||
Blancher A,
|
||
Mesnage V,
|
||
Rivaud-Pechoux S,
|
||
Bertrand A,
|
||
Dupont S,
|
||
Navarro V,
|
||
Roze E,
|
||
Gourfinkel-An I,
|
||
Apartis E</span><br />
|
||
<span class="medgenPMjournal">Rev Neurol (Paris)</span>
|
||
2018 Jan-Feb;174(1-2):56-65.
|
||
Epub 2017 Jul 5
|
||
doi: 10.1016/j.neurol.2017.06.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28688606" target="_blank">28688606</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18996908">A new dominantly inherited pure cerebellar ataxia, SCA 30.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Storey E,
|
||
Bahlo M,
|
||
Fahey M,
|
||
Sisson O,
|
||
Lueck CJ,
|
||
Gardner RJ</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2009 Apr;80(4):408-11.
|
||
Epub 2008 Nov 7
|
||
doi: 10.1136/jnnp.2008.159459.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18996908" target="_blank">18996908</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15855027">Audio-vestibular disturbances in Behcet's patients: report of 62 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kulahli I,
|
||
Balci K,
|
||
Koseoglu E,
|
||
Yuce I,
|
||
Cagli S,
|
||
Senturk M</span><br />
|
||
<span class="medgenPMjournal">Hear Res</span>
|
||
2005 May;203(1-2):28-31.
|
||
doi: 10.1016/j.heares.2004.11.020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15855027" target="_blank">15855027</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypermetric%20saccades%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 (9)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/8296522">Acetazolamide-responsive hereditary paroxysmal ataxia: report of a new family.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Van Bogaert P,
|
||
Van Nechel C,
|
||
Goldman S,
|
||
Szliwowski HB</span><br />
|
||
<span class="medgenPMjournal">Acta Neurol Belg</span>
|
||
1993;93(5):268-75.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8296522" target="_blank">8296522</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypermetric%20saccades%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 (1)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31175630">Eye Movement Abnormalities Are Ubiquitous in the Spinocerebellar Ataxias.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Stephen CD,
|
||
Schmahmann JD</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2019 Dec;18(6):1130-1136.
|
||
doi: 10.1007/s12311-019-01044-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31175630" target="_blank">31175630</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15855027">Audio-vestibular disturbances in Behcet's patients: report of 62 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kulahli I,
|
||
Balci K,
|
||
Koseoglu E,
|
||
Yuce I,
|
||
Cagli S,
|
||
Senturk M</span><br />
|
||
<span class="medgenPMjournal">Hear Res</span>
|
||
2005 May;203(1-2):28-31.
|
||
doi: 10.1016/j.heares.2004.11.020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15855027" target="_blank">15855027</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypermetric%20saccades%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 (2)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37000368">Oculomotor Impairments in Children After Posterior Fossa Tumors Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shurupova MA,
|
||
Latanov AV</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2024 Apr;23(2):444-454.
|
||
Epub 2023 Mar 31
|
||
doi: 10.1007/s12311-023-01553-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37000368" target="_blank">37000368</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18996908">A new dominantly inherited pure cerebellar ataxia, SCA 30.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Storey E,
|
||
Bahlo M,
|
||
Fahey M,
|
||
Sisson O,
|
||
Lueck CJ,
|
||
Gardner RJ</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2009 Apr;80(4):408-11.
|
||
Epub 2008 Nov 7
|
||
doi: 10.1136/jnnp.2008.159459.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18996908" target="_blank">18996908</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15895561">Spinocerebellar ataxia type 20.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Storey E,
|
||
Knight MA,
|
||
Forrest SM,
|
||
Gardner RJ</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2005;4(1):55-7.
|
||
doi: 10.1080/14734220410019048.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15895561" target="_blank">15895561</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14998916">Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Knight MA,
|
||
Gardner RJ,
|
||
Bahlo M,
|
||
Matsuura T,
|
||
Dixon JA,
|
||
Forrest SM,
|
||
Storey E</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2004 May;127(Pt 5):1172-81.
|
||
Epub 2004 Mar 3
|
||
doi: 10.1093/brain/awh139.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14998916" target="_blank">14998916</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14725795">Saccade dysmetria in Williams-Beuren syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van der Geest JN,
|
||
Lagers-van Haselen GC,
|
||
van Hagen JM,
|
||
Govaerts LC,
|
||
de Coo IF,
|
||
de Zeeuw CI,
|
||
Frens MA</span><br />
|
||
<span class="medgenPMjournal">Neuropsychologia</span>
|
||
2004;42(5):569-76.
|
||
doi: 10.1016/j.neuropsychologia.2003.11.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14725795" target="_blank">14725795</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hypermetric%20saccades%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 (6)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
||
|
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|
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<div class=" bottom">
|
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|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
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||
<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>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Hypermetric%20saccades" 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=(%22hypermetric%20saccades%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">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Hypermetric%20saccades" target="_blank">MedlinePlus</a></li></ul></div>
|
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<a href="/pubmed/clinical?term=Hypermetric%20saccades" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Hypermetric%20saccades%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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<ul id="activity">
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d56d5fcde49f3df74434df">Hypermetric saccades</a>
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||
<div class="ralinkpop offscreen_noflow">Hypermetric saccades<div class="brieflinkpopdesc"></div></div>
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||
<div class="tertiary">MedGen</div>
|
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</li>
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<li class="ra_rcd ralinkpopper two_line">
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d56d5e2f30673f7b5d2e7c">Spinocerebellar Ataxia Type 20 - GeneReviews®</a>
|
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<div class="ralinkpop offscreen_noflow">Spinocerebellar Ataxia Type 20 - GeneReviews®<div class="brieflinkpopdesc"></div></div>
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||
<div class="tertiary"></div>
|
||
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|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d56d5c84f3725e5999190c">Table A. [Spinocerebellar Ataxia Type 20: Genes and Databases]. - GeneReviews®</a>
|
||
<div class="ralinkpop offscreen_noflow">Table A. [Spinocerebellar Ataxia Type 20: Genes and Databases]. - GeneReviews®<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary"></div>
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||
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=4" href="/portal/utils/pageresolver.fcgi?recordid=67d56d5c67c23b31e0182c43">Table B. [OMIM Entries for Spinocerebellar Ataxia Type 20 (View All in OMIM)]. -...</a>
|
||
<div class="ralinkpop offscreen_noflow">Table B. [OMIM Entries for Spinocerebellar Ataxia Type 20 (View All in OMIM)]. - GeneReviews®<div class="brieflinkpopdesc"></div></div>
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||
<div class="tertiary"></div>
|
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|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=5" href="/portal/utils/pageresolver.fcgi?recordid=67d56d5bcde49f3df7441db7">Table 1. [Genomic Testing Used in Spinocerebellar Ataxia Type 20]. - GeneReviews...</a>
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