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<!--
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||
UID=373096
|
||
ConceptID=C1836479
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Saccadic smooth pursuit</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>373096</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.">C1836479</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Saccadic pursuit movements; Saccadic slow pursuit</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:0001152">HP:0001152</a></td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln">An abnormality of tracking eye movements in which smooth pursuit is interrupted by an abnormally high number of saccadic movements. [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="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">Saccadic smooth pursuit</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/322909" ref="tree=MeSH" title="MedGen record for Abnormality of ocular smooth pursuit">Abnormality of ocular smooth pursuit</a></span><ul><li><span class="matched_ds">Saccadic smooth pursuit</span><ul><li><span class="TLline"><a href="/medgen/870325" ref="tree=MeSH" title="MedGen record for Intermittent microsaccadic pursuits">Intermittent microsaccadic pursuits</a></span></li><li><span class="TLline"><a href="/medgen/334855" ref="tree=MeSH" title="MedGen record for Microsaccadic pursuit">Microsaccadic pursuit</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>
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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_314039"><div><strong>Episodic ataxia type 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>314039</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.">C1720416</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Episodic ataxia is a genetically heterogeneous neurologic condition characterized by spells of incoordination and imbalance, often associated with progressive ataxia. Episodic ataxia type 2 is the most common form of EA (Jen et al., 2007). For a discussion of genetic heterogeneity of episodic ataxia, see EA1 (160120).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/314039">Condition Record</a></div></div>
|
||
<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_333403"><div><strong>Fragile X-associated tremor/ataxia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>333403</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.">C1839780</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">FMR1 disorders include fragile X syndrome (FXS), fragile X-associated tremor/ataxia syndrome (FXTAS), and fragile X-associated primary ovarian insufficiency (FXPOI). Fragile X syndrome occurs in individuals with an FMR1 full mutation or other loss-of-function variant and is nearly always characterized in affected males by developmental delay and intellectual disability along with a variety of behavioral issues. Autism spectrum disorder is present in 50%-70% of individuals with FXS. Affected males may have characteristic craniofacial features (which become more obvious with age) and medical problems including hypotonia, gastroesophageal reflux, strabismus, seizures, sleep disorders, joint laxity, pes planus, scoliosis, and recurrent otitis media. Adults may have mitral valve prolapse or aortic root dilatation. The physical and behavioral features seen in males with FXS have been reported in females heterozygous for the FMR1 full mutation, but with lower frequency and milder involvement. FXTAS occurs in individuals who have an FMR1 premutation and is characterized by late-onset, progressive cerebellar ataxia and intention tremor followed by cognitive impairment. Psychiatric disorders are common. Age of onset is typically between 60 and 65 years and is more common among males who are hemizygous for the premutation (40%) than among females who are heterozygous for the premutation (16%-20%). FXPOI, defined as hypergonadotropic hypogonadism before age 40 years, has been observed in 20% of women who carry a premutation allele compared to 1% in the general population.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/333403">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_339504"><div><strong>Spinocerebellar ataxia type 19/22</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>339504</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.">C1846367</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spinocerebellar ataxia-19 (SCA19) is an autosomal dominant disorder characterized by progressive cerebellar ataxia with a variable age of onset (age 2 years to late adulthood). Other neurologic manifestations include developmental delay and cognitive impairment; movement disorders including myoclonus, dystonia, rigidity, and bradykinesia; and seizures. For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/339504">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_342870"><div><strong>Juvenile primary lateral sclerosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>342870</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.">C1853396</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">ALS2-related disorder involves retrograde degeneration of the upper motor neurons of the pyramidal tracts and comprises a clinical continuum of the following three phenotypes: Infantile ascending hereditary spastic paraplegia (IAHSP), characterized by onset of spasticity with increased reflexes and sustained clonus of the lower limbs within the first two years of life, progressive weakness and spasticity of the upper limbs by age seven to eight years, and wheelchair dependence in the second decade with progression toward severe spastic tetraparesis and a pseudobulbar syndrome caused by progressive cranial nerve involvement. Juvenile primary lateral sclerosis (JPLS), characterized by upper motor neuron findings of pseudobulbar palsy and spastic quadriplegia without dementia or cerebellar, extrapyramidal, or sensory signs. Juvenile amyotrophic lateral sclerosis (JALS or ALS2), characterized by onset between ages three and 20 years. All affected individuals show a spastic pseudobulbar syndrome (spasticity of speech and swallowing) together with spastic paraplegia. Some individuals are bedridden by age 12 to 50 years.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/342870">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."><span class="highlight" style="background-color:">C1853761</span></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="divPopper rprt" id="rdis_349134"><div><strong>Autosomal recessive spinocerebellar ataxia 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>349134</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.">C1859298</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spinocerebellar ataxia-2 (SCAR2) is a neurologic disorder characterized by onset of impaired motor development and ataxic gait in early childhood. Additional features often include loss of fine motor skills, dysarthria, nystagmus, cerebellar signs, and delayed cognitive development with intellectual disability. Brain imaging shows cerebellar atrophy. Overall, the disorder is non- or slowly progressive, with survival into adulthood (summary by Jobling et al., 2015).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/349134">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_482853"><div><strong>Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>482853</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.">C3281223</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The phenotypic spectrum associated with biallelic RFC1 AAGGG repeat expansion encompasses a range including (1) typical cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS); (2) cerebellar, sensory, and vestibular impairment; (3) more limited phenotypes involving predominantly or exclusively one of the systems involved in balance control; (4) autonomic dysfunction; and (5) cough. Onset begins after age 35 years. In a retrospective study of 100 affected individuals after ten years of disease duration, two thirds had clinical features of CANVAS; 16 had a complex sensory ataxia with cerebellar or vestibular involvement; and 15 had a sensory neuropathy as the only clinically detectable manifestation.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/482853">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_816656"><div><strong>Autosomal recessive spinocerebellar ataxia 15</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>816656</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.">C3810326</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spinocerebellar ataxia-15 (SCAR15) is characterized by early-onset ataxia, cognitive impairment, dysarthria, and developmental delay. Variable features include seizures, nystagmus, and abnormal reflexes (Seidahmed et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/816656">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_902592"><div><strong>Spinocerebellar ataxia type 42</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>902592</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.">C4225205</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spinocerebellar ataxia-42 (SCA42) is an autosomal dominant neurologic disorder characterized predominantly by gait instability and additional cerebellar signs such as dysarthria, nystagmus, and saccadic pursuits. The age at onset and severity of the disorder is highly variable. The disorder is slowly progressive (Coutelier et al., 2015). For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/902592">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_1631337"><div><strong>Leukodystrophy, hypomyelinating, 16</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1631337</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.">C4693779</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypomyelinating leukodystrophy-16 (HLD16) is an autosomal dominant neurologic disorder characterized by onset of hypotonia, nystagmus, and mildly delayed motor development in infancy. Affected individuals have motor disabilities, including ataxic or broad-based gait, hyperreflexia, intention tremor, dysmetria, and a mild pyramidal syndrome. Some patients have cognitive impairment, whereas others may have normal cognition or mild intellectual disability with speech difficulties. Brain imaging typically shows hypomyelination, leukodystrophy, and thin corpus callosum (summary by Simons et al., 2017). For a general phenotypic description and a discussion of genetic heterogeneity of hypomyelinating leukodystrophy, see 312080.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1631337">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794263"><div><strong>Spastic paraplegia 85, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794263</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.">C5562053</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spastic paraplegia-85 (SPG85) is a neurologic disorder characterized by the onset of motor symptoms in the first few years of life. Affected individuals have spasticity and hyperreflexia of the lower limbs resulting in gait abnormalities. Older patients may have upper limb involvement and demonstrate axonal polyneuropathy. Additional features include optic atrophy, dysarthria, dysphagia, ataxia, and urinary incontinence. Brain imaging may show cerebellar atrophy (summary by Wagner et al., 2019). For a discussion of genetic heterogeneity of autosomal recessive spastic paraplegia, see SPG5A (270800).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794263">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="divPopper rprt" id="rdis_1824073"><div><strong>Spastic paraplegia 79A, autosomal dominant, with ataxia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1824073</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.">C5774300</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal dominant spastic paraplegia-79A with ataxia (SPG79A) is a slowly progressive neurodegenerative disorder characterized predominantly by cerebellar and/or sensory ataxia and spasticity of the lower limbs leading to gait difficulties. The onset is usually in adulthood (median age of 49 years), but can range from childhood to age 70. Additional common features include sensorimotor neuropathy and visual impairment with optic atrophy. The disorder is slowly progressive (Park et al., 2022).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1824073">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_816656" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive spinocerebellar ataxia 15</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_349134" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive spinocerebellar ataxia 2</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_482853" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_314039" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Episodic ataxia type 2</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (15)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_333403" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Fragile X-associated tremor/ataxia syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_342870" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Juvenile primary lateral sclerosis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1631337" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Leukodystrophy, hypomyelinating, 16</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1824073" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spastic paraplegia 79A, autosomal dominant, with ataxia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794263" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spastic paraplegia 85, autosomal recessive</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_339504" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 19/22</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_902592" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 42</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_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>
|
||
<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></span></div></div>
|
||
</div>
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||
|
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<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34864777">Vestibular Rehabilitation for Peripheral Vestibular Hypofunction: An Updated Clinical Practice Guideline From the Academy of Neurologic Physical Therapy of the American Physical Therapy Association.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hall CD,
|
||
Herdman SJ,
|
||
Whitney SL,
|
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Anson ER,
|
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Carender WJ,
|
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Hoppes CW,
|
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Cass SP,
|
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Christy JB,
|
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Cohen HS,
|
||
Fife TD,
|
||
Furman JM,
|
||
Shepard NT,
|
||
Clendaniel RA,
|
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Dishman JD,
|
||
Goebel JA,
|
||
Meldrum D,
|
||
Ryan C,
|
||
Wallace RL,
|
||
Woodward NJ</span><br />
|
||
<span class="medgenPMjournal">J Neurol Phys Ther</span>
|
||
2022 Apr 1;46(2):118-177.
|
||
doi: 10.1097/NPT.0000000000000382.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34864777" target="_blank">34864777</a><a href="/pmc/articles/PMC8920012" 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 class="nl"><a target="_blank" href="/pubmed/26913496">Vestibular Rehabilitation for Peripheral Vestibular Hypofunction: An Evidence-Based Clinical Practice Guideline: FROM THE AMERICAN PHYSICAL THERAPY ASSOCIATION NEUROLOGY SECTION.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hall CD,
|
||
Herdman SJ,
|
||
Whitney SL,
|
||
Cass SP,
|
||
Clendaniel RA,
|
||
Fife TD,
|
||
Furman JM,
|
||
Getchius TS,
|
||
Goebel JA,
|
||
Shepard NT,
|
||
Woodhouse SN</span><br />
|
||
<span class="medgenPMjournal">J Neurol Phys Ther</span>
|
||
2016 Apr;40(2):124-55.
|
||
doi: 10.1097/NPT.0000000000000120.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26913496" target="_blank">26913496</a><a href="/pmc/articles/PMC4795094" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(saccadic%20smooth%20pursuit)%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 (19)</a></div></div>
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</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/32797299">Acute binocular diplopia: peripheral or central?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kremmyda O,
|
||
Frenzel C,
|
||
Hüfner K,
|
||
Goldschagg N,
|
||
Brem C,
|
||
Linn J,
|
||
Strupp M</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2020 Dec;267(Suppl 1):136-142.
|
||
Epub 2020 Aug 14
|
||
doi: 10.1007/s00415-020-10088-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32797299" target="_blank">32797299</a><a href="/pmc/articles/PMC7718182" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30552638">What Is Behind Cerebellar Vertigo and Dizziness?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Feil K,
|
||
Strobl R,
|
||
Schindler A,
|
||
Krafczyk S,
|
||
Goldschagg N,
|
||
Frenzel C,
|
||
Glaser M,
|
||
Schöberl F,
|
||
Zwergal A,
|
||
Strupp M</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2019 Jun;18(3):320-332.
|
||
doi: 10.1007/s12311-018-0992-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30552638" target="_blank">30552638</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19725817">Altered vision during motion: an unusual symptom of cerebellar dysfunction, quantifiable by a simple clinical test.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kaeser PF,
|
||
Borruat FX</span><br />
|
||
<span class="medgenPMjournal">Acta Ophthalmol</span>
|
||
2010 Nov;88(7):791-6.
|
||
doi: 10.1111/j.1755-3768.2009.01544.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19725817" target="_blank">19725817</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7150679">Saccadic eye movements of schizophrenic patients measured by reflected light technique.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Levin S,
|
||
Jones A,
|
||
Stark L,
|
||
Merrin EL,
|
||
Holzman PS</span><br />
|
||
<span class="medgenPMjournal">Biol Psychiatry</span>
|
||
1982 Nov;17(11):1277-87.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7150679" target="_blank">7150679</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7417059">Effect of aging on eye tracking.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Spooner JW,
|
||
Sakala SM,
|
||
Baloh RW</span><br />
|
||
<span class="medgenPMjournal">Arch Neurol</span>
|
||
1980 Sep;37(9):575-6.
|
||
doi: 10.1001/archneur.1980.00500580071012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7417059" target="_blank">7417059</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Saccadic%20smooth%20pursuit%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 (5)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34784643">Central Ocular Motor Disorders: Clinical and Topographic Anatomical Diagnosis, Syndromes and Underlying Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Strupp ML,
|
||
Straumann D,
|
||
Helmchen C</span><br />
|
||
<span class="medgenPMjournal">Klin Monbl Augenheilkd</span>
|
||
2021 Nov;238(11):1197-1211.
|
||
Epub 2021 Nov 16
|
||
doi: 10.1055/a-1654-0632.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34784643" target="_blank">34784643</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32797299">Acute binocular diplopia: peripheral or central?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kremmyda O,
|
||
Frenzel C,
|
||
Hüfner K,
|
||
Goldschagg N,
|
||
Brem C,
|
||
Linn J,
|
||
Strupp M</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2020 Dec;267(Suppl 1):136-142.
|
||
Epub 2020 Aug 14
|
||
doi: 10.1007/s00415-020-10088-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32797299" target="_blank">32797299</a><a href="/pmc/articles/PMC7718182" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32157568">A Variation in FGF14 Is Associated with Downbeat Nystagmus in a Genome-Wide Association Study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Strupp M,
|
||
Maul S,
|
||
Konte B,
|
||
Hartmann AM,
|
||
Giegling I,
|
||
Wollenteit S,
|
||
Feil K,
|
||
Rujescu D</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2020 Jun;19(3):348-357.
|
||
doi: 10.1007/s12311-020-01113-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32157568" target="_blank">32157568</a><a href="/pmc/articles/PMC7198638" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30552638">What Is Behind Cerebellar Vertigo and Dizziness?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Feil K,
|
||
Strobl R,
|
||
Schindler A,
|
||
Krafczyk S,
|
||
Goldschagg N,
|
||
Frenzel C,
|
||
Glaser M,
|
||
Schöberl F,
|
||
Zwergal A,
|
||
Strupp M</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2019 Jun;18(3):320-332.
|
||
doi: 10.1007/s12311-018-0992-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30552638" target="_blank">30552638</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25522697">Esophoria or esotropia in adulthood: a sign of cerebellar dysfunction?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hüfner K,
|
||
Frenzel C,
|
||
Kremmyda O,
|
||
Adrion C,
|
||
Bardins S,
|
||
Glasauer S,
|
||
Brandt T,
|
||
Strupp M</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2015 Mar;262(3):585-92.
|
||
Epub 2014 Dec 19
|
||
doi: 10.1007/s00415-014-7614-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25522697" target="_blank">25522697</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Saccadic%20smooth%20pursuit%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 (14)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/9579670">Stimulus predictability and the gap effect on pre-saccadic smooth pursuit.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Knox PC</span><br />
|
||
<span class="medgenPMjournal">Neuroreport</span>
|
||
1998 Mar 30;9(5):809-12.
|
||
doi: 10.1097/00001756-199803300-00008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9579670" target="_blank">9579670</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3122069">Bedside and electro-oculographic analysis of abnormal ocular movements in spinocerebellar degenerations: effects of thyrotropin-releasing hormone.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yamamoto H,
|
||
Saito S,
|
||
Sobue I</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
1988 Jan;38(1):110-4.
|
||
doi: 10.1212/wnl.38.1.110.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3122069" target="_blank">3122069</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6127062">Identification of abnormal patterns in eye movements of schizophrenic patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Levin S,
|
||
Jones A,
|
||
Stark L,
|
||
Merrin EL,
|
||
Holzman PS</span><br />
|
||
<span class="medgenPMjournal">Arch Gen Psychiatry</span>
|
||
1982 Oct;39(10):1125-30.
|
||
doi: 10.1001/archpsyc.1982.04290100005002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6127062" target="_blank">6127062</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Saccadic%20smooth%20pursuit%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 (3)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34784643">Central Ocular Motor Disorders: Clinical and Topographic Anatomical Diagnosis, Syndromes and Underlying Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Strupp ML,
|
||
Straumann D,
|
||
Helmchen C</span><br />
|
||
<span class="medgenPMjournal">Klin Monbl Augenheilkd</span>
|
||
2021 Nov;238(11):1197-1211.
|
||
Epub 2021 Nov 16
|
||
doi: 10.1055/a-1654-0632.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34784643" target="_blank">34784643</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32797299">Acute binocular diplopia: peripheral or central?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kremmyda O,
|
||
Frenzel C,
|
||
Hüfner K,
|
||
Goldschagg N,
|
||
Brem C,
|
||
Linn J,
|
||
Strupp M</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2020 Dec;267(Suppl 1):136-142.
|
||
Epub 2020 Aug 14
|
||
doi: 10.1007/s00415-020-10088-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32797299" target="_blank">32797299</a><a href="/pmc/articles/PMC7718182" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9579670">Stimulus predictability and the gap effect on pre-saccadic smooth pursuit.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Knox PC</span><br />
|
||
<span class="medgenPMjournal">Neuroreport</span>
|
||
1998 Mar 30;9(5):809-12.
|
||
doi: 10.1097/00001756-199803300-00008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9579670" target="_blank">9579670</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8539013">Relation between backward masking deficits and smooth pursuit dysfunction in schizophrenia?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Allen JS</span><br />
|
||
<span class="medgenPMjournal">Optom Vis Sci</span>
|
||
1995 Jul;72(7):493-501.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8539013" target="_blank">8539013</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Saccadic%20smooth%20pursuit%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 (4)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32797299">Acute binocular diplopia: peripheral or central?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kremmyda O,
|
||
Frenzel C,
|
||
Hüfner K,
|
||
Goldschagg N,
|
||
Brem C,
|
||
Linn J,
|
||
Strupp M</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2020 Dec;267(Suppl 1):136-142.
|
||
Epub 2020 Aug 14
|
||
doi: 10.1007/s00415-020-10088-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32797299" target="_blank">32797299</a><a href="/pmc/articles/PMC7718182" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27401169">Evaluation of the Tobii EyeX Eye tracking controller and Matlab toolkit for research.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gibaldi A,
|
||
Vanegas M,
|
||
Bex PJ,
|
||
Maiello G</span><br />
|
||
<span class="medgenPMjournal">Behav Res Methods</span>
|
||
2017 Jun;49(3):923-946.
|
||
doi: 10.3758/s13428-016-0762-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27401169" target="_blank">27401169</a><a href="/pmc/articles/PMC5429393" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9579670">Stimulus predictability and the gap effect on pre-saccadic smooth pursuit.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Knox PC</span><br />
|
||
<span class="medgenPMjournal">Neuroreport</span>
|
||
1998 Mar 30;9(5):809-12.
|
||
doi: 10.1097/00001756-199803300-00008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9579670" target="_blank">9579670</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2242390">Smooth pursuit eye movements of normal and schizophrenic subjects tracking an unpredictable target.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Allen JS,
|
||
Matsunaga K,
|
||
Hacisalihzade S,
|
||
Stark L</span><br />
|
||
<span class="medgenPMjournal">Biol Psychiatry</span>
|
||
1990 Oct 15;28(8):705-20.
|
||
doi: 10.1016/0006-3223(90)90457-d.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2242390" target="_blank">2242390</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7070792">Oculomotor abnormalities after labyrinthine and cerebellar lesion. A case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cherubino M,
|
||
Mira E,
|
||
Mevio E</span><br />
|
||
<span class="medgenPMjournal">ORL J Otorhinolaryngol Relat Spec</span>
|
||
1982;44(1):24-35.
|
||
doi: 10.1159/000275564.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7070792" target="_blank">7070792</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Saccadic%20smooth%20pursuit%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 (5)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
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|
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|
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||
|
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|
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</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
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|
||
|
||
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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=Saccadic%20smooth%20pursuit" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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|
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<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>
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