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<!--
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UID=335355
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ConceptID=C1846176
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Hyperactive deep tendon reflexes</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>335355</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.">C1846176</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><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:0006801">HP:0006801</a></td></tr>
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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">Hyperactive deep tendon reflexes</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/868417" ref="tree=MeSH" title="MedGen record for Abnormal nervous system physiology">Abnormal nervous system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/10113" ref="tree=MeSH" title="MedGen record for Movement disorder">Movement disorder</a></span><ul><li><span class="TLline"><a href="/medgen/19707" ref="tree=MeSH" title="MedGen record for Abnormal reflex">Abnormal reflex</a></span><ul><li><span class="TLline"><a href="/medgen/57738" ref="tree=MeSH" title="MedGen record for Hyperreflexia">Hyperreflexia</a></span><ul><li><span class="matched_ds">Hyperactive deep tendon reflexes</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_44131"><div><strong>Galactosylceramide beta-galactosidase deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>44131</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.">C0023521</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Krabbe disease comprises a spectrum ranging from infantile-onset disease (i.e., onset of extreme irritability, spasticity, and developmental delay before age 12 months) to later-onset disease (i.e., onset of manifestations after age 12 months and as late as the seventh decade). Although historically 85%-90% of symptomatic individuals with Krabbe disease diagnosed by enzyme activity alone have infantile-onset Krabbe disease and 10%-15% have later-onset Krabbe disease, the experience with newborn screening (NBS) suggests that the proportion of individuals with possible later-onset Krabbe disease is higher than previously thought. Infantile-onset Krabbe disease is characterized by normal development in the first few months followed by rapid severe neurologic deterioration; the average age of death is 24 months (range 8 months to 9 years). Later-onset Krabbe disease is much more variable in its presentation and disease course.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/44131">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_167236"><div><strong>Oculodentodigital dysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>167236</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.">C0812437</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Oculodentodigital dysplasia (ODDD) is characterized by a typical facial appearance and variable involvement of the eyes, dentition, and fingers. Characteristic facial features include a narrow, pinched nose with hypoplastic alae nasi, prominent columella and thin anteverted nares together with a narrow nasal bridge, and prominent epicanthic folds giving the impression of hypertelorism. The teeth are usually small and carious. Typical eye findings include microphthalmia and microcornea. The characteristic digital malformation is complete syndactyly of the fourth and fifth fingers (syndactyly type III) but the third finger may be involved and associated camptodactyly is a common finding (summary by Judisch et al., 1979). Neurologic abnormalities are sometimes associated (Gutmann et al., 1991), and lymphedema has been reported in some patients with ODDD (Brice et al., 2013). See review by De Bock et al. (2013). Genetic Heterogeneity of Oculodentodigital Syndrome An autosomal recessive form of ODDD (257850) is also caused by mutation in the GJA1 gene, but the majority of cases are autosomal dominant.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/167236">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_230896"><div><strong>Ataxia-pancytopenia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>230896</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.">C1327919</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">SAMD9L ataxia-pancytopenia (ATXPC) syndrome is characterized by cerebellar ataxia, variable hematologic cytopenias, and predisposition to marrow failure, myelodysplasia, and myeloid leukemia, sometimes associated with monosomy 7. The onset of hematologic abnormalities has been reported as early as age three months. The cytopenias in all cell lineages range from mild to very severe. Onset of neurologic impairment is variable. Nystagmus, dysmetria, increased deep tendon reflexes, and clonus are common. Gait impairment and other neurologic abnormalities are slowly progressive.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/230896">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_344468"><div><strong>Intellectual disability, autosomal recessive 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>344468</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.">C1855304</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the PRSS12 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/344468">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_395174"><div><strong>Infantile choroidocerebral calcification syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>395174</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.">C1859092</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">This syndrome has characteristics of intellectual deficit, calcification of the choroid plexus and elevated levels of cerebrospinal fluid protein. It has been described in two sibships from two unrelated families. The seven children of one of the sibships were born to consanguineous parents. Some patients also had strabismus, hyperactive deep tendon reflexes and foot deformities.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/395174">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_413474"><div><strong>Neuropathy, hereditary sensory and autonomic, type 2B</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>413474</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.">C2751092</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hereditary sensory and autonomic neuropathy type II (HSAN2) is characterized by progressively reduced sensation to pain, temperature, and touch. Onset can be at birth and is often before puberty. The sensory deficit is predominantly distal with the lower limbs more severely affected than the upper limbs. Over time sensory function becomes severely reduced. Unnoticed injuries and neuropathic skin promote ulcerations and infections that result in spontaneous amputation of digits or the need for surgical amputation. Osteomyelitis is common. Painless fractures can complicate the disease. Autonomic disturbances are variable and can include hyperhidrosis, tonic pupils, and urinary incontinence in those with more advanced disease.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/413474">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_462419"><div><strong>Chromosome 17p13.1 deletion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>462419</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.">C3151069</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/462419">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934760"><div><strong>Heart and brain malformation syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934760</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.">C4310793</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Heart and brain malformation syndrome (HBMS) is a severe autosomal recessive multiple congenital anomaly syndrome characterized by profoundly delayed psychomotor development, dysmorphic facial features, microphthalmia, cardiac malformations, mainly septal defects, and brain malformations, including Dandy-Walker malformation (summary by Shaheen et al., 2016). Homozygous mutation in the SMG9 gene can also cause neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies (NEDITPDO; 619995), a less severe neurodevelopmental disorder.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934760">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1680057"><div><strong>Cerebellar, ocular, craniofacial, and genital syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1680057</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.">C5193118</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cerebellar, ocular, craniofacial, and genital syndrome (COFG) is characterized by moderate to severe developmental delay and impaired intellectual development, severe cerebellar hypoplasia, a noticeably short forehead, medially sparse/flared and laterally extended eyebrows, corneal dystrophy, underdeveloped labioscrotal folds, and tufts of hair extruding from the lactiferous ducts with breast and nipple underdevelopment. Additional features such as pontine involvement, retinal degeneration, anteverted nares, and low-set ears have been variably observed (Rad et al., 2019).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1680057">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1798947"><div><strong>Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1798947</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.">C5567524</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">TANGO2 deficiency is characterized by developmental delay, intellectual disability, gait incoordination, speech difficulties, seizures, and hypothyroidism. Most individuals have TANGO2 spells, non-life-threatening paroxysmal worsening of baseline symptoms, including sudden onset of hypotonia, ataxia with loss of balance, head and body tilt, increased dysarthria, drooling, lethargy, and disorientation. In addition, life-threatening acute metabolic crises can occur, including rhabdomyolysis with elevated creatine phosphokinase and liver transaminases, hypoglycemia, prolonged QTc on EKG, ventricular arrhythmias, and/or cardiomyopathy.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1798947">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_230896" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ataxia-pancytopenia syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1680057" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebellar, ocular, craniofacial, and genital syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_462419" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chromosome 17p13.1 deletion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_44131" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Galactosylceramide beta-galactosidase deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934760" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Heart and brain malformation syndrome</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (10)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_395174" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Infantile choroidocerebral calcification syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_344468" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, autosomal recessive 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_413474" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neuropathy, hereditary sensory and autonomic, type 2B</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_167236" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Oculodentodigital dysplasia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1798947" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome</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/39982496">Diagnostic utility of deep tendon reflex responses in rectus femoris and triceps brachii in fibromyalgia: a clinical and electrophysiological study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Coskun Benlidayi I,
|
||
Deniz V,
|
||
Ornek C,
|
||
Sariyildiz A</span><br />
|
||
<span class="medgenPMjournal">Rheumatol Int</span>
|
||
2025 Feb 21;45(3):57.
|
||
doi: 10.1007/s00296-025-05808-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39982496" target="_blank">39982496</a><a href="/pmc/articles/PMC11845418" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22hyperactive%20deep%20tendon%20reflexes%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/39982496">Diagnostic utility of deep tendon reflex responses in rectus femoris and triceps brachii in fibromyalgia: a clinical and electrophysiological study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Coskun Benlidayi I,
|
||
Deniz V,
|
||
Ornek C,
|
||
Sariyildiz A</span><br />
|
||
<span class="medgenPMjournal">Rheumatol Int</span>
|
||
2025 Feb 21;45(3):57.
|
||
doi: 10.1007/s00296-025-05808-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39982496" target="_blank">39982496</a><a href="/pmc/articles/PMC11845418" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/39639192">A rare case of recurrent spinal hydatid cyst in a 17-year-old man with neurological deficits and balance impairment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Farjam M,
|
||
Changizi F,
|
||
Ebrahimzadeh K,
|
||
Sabeti S,
|
||
Bidari Zerehpoush F,
|
||
Javandoust Gharehbagh F,
|
||
Alavi Darazam I</span><br />
|
||
<span class="medgenPMjournal">BMC Infect Dis</span>
|
||
2024 Dec 6;24(1):1392.
|
||
doi: 10.1186/s12879-024-10286-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39639192" target="_blank">39639192</a><a href="/pmc/articles/PMC11622484" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33175256">Spinocerebellar ataxia type 23 (SCA23): a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wu F,
|
||
Wang X,
|
||
Li X,
|
||
Teng H,
|
||
Tian T,
|
||
Bai J</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2021 Dec;268(12):4630-4645.
|
||
Epub 2020 Nov 11
|
||
doi: 10.1007/s00415-020-10297-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33175256" target="_blank">33175256</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18262342">Pure primary lateral sclerosis--Case reports.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tomik B,
|
||
Zur KA,
|
||
Szczudlik A</span><br />
|
||
<span class="medgenPMjournal">Clin Neurol Neurosurg</span>
|
||
2008 Apr;110(4):387-91.
|
||
Epub 2008 Feb 8
|
||
doi: 10.1016/j.clineuro.2007.12.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18262342" target="_blank">18262342</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10660022">Medically treated intraspinal "Brucella" granuloma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bingöl A,
|
||
Yücemen N,
|
||
Meço O</span><br />
|
||
<span class="medgenPMjournal">Surg Neurol</span>
|
||
1999 Dec;52(6):570-6.
|
||
doi: 10.1016/s0090-3019(99)00110-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10660022" target="_blank">10660022</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hyperactive%20deep%20tendon%20reflexes%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (8)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39982496">Diagnostic utility of deep tendon reflex responses in rectus femoris and triceps brachii in fibromyalgia: a clinical and electrophysiological study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Coskun Benlidayi I,
|
||
Deniz V,
|
||
Ornek C,
|
||
Sariyildiz A</span><br />
|
||
<span class="medgenPMjournal">Rheumatol Int</span>
|
||
2025 Feb 21;45(3):57.
|
||
doi: 10.1007/s00296-025-05808-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39982496" target="_blank">39982496</a><a href="/pmc/articles/PMC11845418" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32988246">Multiple sclerosis attack case presenting with pseudo-vestibular neuritis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Surmeli R,
|
||
Surmeli M,
|
||
Yalcin AD,
|
||
Yilmaz AAS,
|
||
Kucuk F</span><br />
|
||
<span class="medgenPMjournal">Int J Neurosci</span>
|
||
2022 Jun;132(6):601-605.
|
||
Epub 2020 Oct 6
|
||
doi: 10.1080/00207454.2020.1829617.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32988246" target="_blank">32988246</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33175256">Spinocerebellar ataxia type 23 (SCA23): a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wu F,
|
||
Wang X,
|
||
Li X,
|
||
Teng H,
|
||
Tian T,
|
||
Bai J</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2021 Dec;268(12):4630-4645.
|
||
Epub 2020 Nov 11
|
||
doi: 10.1007/s00415-020-10297-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33175256" target="_blank">33175256</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18262342">Pure primary lateral sclerosis--Case reports.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tomik B,
|
||
Zur KA,
|
||
Szczudlik A</span><br />
|
||
<span class="medgenPMjournal">Clin Neurol Neurosurg</span>
|
||
2008 Apr;110(4):387-91.
|
||
Epub 2008 Feb 8
|
||
doi: 10.1016/j.clineuro.2007.12.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18262342" target="_blank">18262342</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1875026">Jitteriness beyond the neonatal period: a benign pattern of movement in infancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shuper A,
|
||
Zalzberg J,
|
||
Weitz R,
|
||
Mimouni M</span><br />
|
||
<span class="medgenPMjournal">J Child Neurol</span>
|
||
1991 Jul;6(3):243-5.
|
||
doi: 10.1177/088307389100600307.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1875026" target="_blank">1875026</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hyperactive%20deep%20tendon%20reflexes%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 (16)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39639192">A rare case of recurrent spinal hydatid cyst in a 17-year-old man with neurological deficits and balance impairment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Farjam M,
|
||
Changizi F,
|
||
Ebrahimzadeh K,
|
||
Sabeti S,
|
||
Bidari Zerehpoush F,
|
||
Javandoust Gharehbagh F,
|
||
Alavi Darazam I</span><br />
|
||
<span class="medgenPMjournal">BMC Infect Dis</span>
|
||
2024 Dec 6;24(1):1392.
|
||
doi: 10.1186/s12879-024-10286-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39639192" target="_blank">39639192</a><a href="/pmc/articles/PMC11622484" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15235352">Spastic diplegia and other motor disturbances in infants receiving interferon-alpha.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Michaud AP,
|
||
Bauman NM,
|
||
Burke DK,
|
||
Manaligod JM,
|
||
Smith RJ</span><br />
|
||
<span class="medgenPMjournal">Laryngoscope</span>
|
||
2004 Jul;114(7):1231-6.
|
||
doi: 10.1097/00005537-200407000-00017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15235352" target="_blank">15235352</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12760433">Central pontine and extrapontine myelinolysis owing to disequilibrium syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aydin OF,
|
||
Uner C,
|
||
Senbil N,
|
||
Bek K,
|
||
Erdoğan O,
|
||
Gürer YK</span><br />
|
||
<span class="medgenPMjournal">J Child Neurol</span>
|
||
2003 Apr;18(4):292-6.
|
||
doi: 10.1177/08830738030180040701.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12760433" target="_blank">12760433</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10660022">Medically treated intraspinal "Brucella" granuloma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bingöl A,
|
||
Yücemen N,
|
||
Meço O</span><br />
|
||
<span class="medgenPMjournal">Surg Neurol</span>
|
||
1999 Dec;52(6):570-6.
|
||
doi: 10.1016/s0090-3019(99)00110-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10660022" target="_blank">10660022</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3687370">Vaccine-associated contact paralytic poliomyelitis with atypical neurological presentation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Arlazoroff A,
|
||
Bleicher Z,
|
||
Klein C,
|
||
Vure E,
|
||
Lahat E,
|
||
Gross B,
|
||
Handsher R</span><br />
|
||
<span class="medgenPMjournal">Acta Neurol Scand</span>
|
||
1987 Sep;76(3):210-4.
|
||
doi: 10.1111/j.1600-0404.1987.tb03569.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3687370" target="_blank">3687370</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hyperactive%20deep%20tendon%20reflexes%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 (6)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33175256">Spinocerebellar ataxia type 23 (SCA23): a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wu F,
|
||
Wang X,
|
||
Li X,
|
||
Teng H,
|
||
Tian T,
|
||
Bai J</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2021 Dec;268(12):4630-4645.
|
||
Epub 2020 Nov 11
|
||
doi: 10.1007/s00415-020-10297-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33175256" target="_blank">33175256</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18262342">Pure primary lateral sclerosis--Case reports.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tomik B,
|
||
Zur KA,
|
||
Szczudlik A</span><br />
|
||
<span class="medgenPMjournal">Clin Neurol Neurosurg</span>
|
||
2008 Apr;110(4):387-91.
|
||
Epub 2008 Feb 8
|
||
doi: 10.1016/j.clineuro.2007.12.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18262342" target="_blank">18262342</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10660022">Medically treated intraspinal "Brucella" granuloma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bingöl A,
|
||
Yücemen N,
|
||
Meço O</span><br />
|
||
<span class="medgenPMjournal">Surg Neurol</span>
|
||
1999 Dec;52(6):570-6.
|
||
doi: 10.1016/s0090-3019(99)00110-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10660022" target="_blank">10660022</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1875026">Jitteriness beyond the neonatal period: a benign pattern of movement in infancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shuper A,
|
||
Zalzberg J,
|
||
Weitz R,
|
||
Mimouni M</span><br />
|
||
<span class="medgenPMjournal">J Child Neurol</span>
|
||
1991 Jul;6(3):243-5.
|
||
doi: 10.1177/088307389100600307.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1875026" target="_blank">1875026</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hyperactive%20deep%20tendon%20reflexes%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/39982496">Diagnostic utility of deep tendon reflex responses in rectus femoris and triceps brachii in fibromyalgia: a clinical and electrophysiological study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Coskun Benlidayi I,
|
||
Deniz V,
|
||
Ornek C,
|
||
Sariyildiz A</span><br />
|
||
<span class="medgenPMjournal">Rheumatol Int</span>
|
||
2025 Feb 21;45(3):57.
|
||
doi: 10.1007/s00296-025-05808-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39982496" target="_blank">39982496</a><a href="/pmc/articles/PMC11845418" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/39639192">A rare case of recurrent spinal hydatid cyst in a 17-year-old man with neurological deficits and balance impairment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Farjam M,
|
||
Changizi F,
|
||
Ebrahimzadeh K,
|
||
Sabeti S,
|
||
Bidari Zerehpoush F,
|
||
Javandoust Gharehbagh F,
|
||
Alavi Darazam I</span><br />
|
||
<span class="medgenPMjournal">BMC Infect Dis</span>
|
||
2024 Dec 6;24(1):1392.
|
||
doi: 10.1186/s12879-024-10286-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39639192" target="_blank">39639192</a><a href="/pmc/articles/PMC11622484" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18262342">Pure primary lateral sclerosis--Case reports.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tomik B,
|
||
Zur KA,
|
||
Szczudlik A</span><br />
|
||
<span class="medgenPMjournal">Clin Neurol Neurosurg</span>
|
||
2008 Apr;110(4):387-91.
|
||
Epub 2008 Feb 8
|
||
doi: 10.1016/j.clineuro.2007.12.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18262342" target="_blank">18262342</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7572078">Amyotrophic lateral sclerosis with marked neurological asymmetry: clinicopathological study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mochizuki Y,
|
||
Mizutani T,
|
||
Takasu T</span><br />
|
||
<span class="medgenPMjournal">Acta Neuropathol</span>
|
||
1995;90(1):44-50.
|
||
doi: 10.1007/BF00294458.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7572078" target="_blank">7572078</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1875026">Jitteriness beyond the neonatal period: a benign pattern of movement in infancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shuper A,
|
||
Zalzberg J,
|
||
Weitz R,
|
||
Mimouni M</span><br />
|
||
<span class="medgenPMjournal">J Child Neurol</span>
|
||
1991 Jul;6(3):243-5.
|
||
doi: 10.1177/088307389100600307.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1875026" target="_blank">1875026</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hyperactive%20deep%20tendon%20reflexes%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 (7)</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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|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
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|
||
|
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|
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<div class="portlet 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=Hyperactive%20deep%20tendon%20reflexes" target="_blank">ClinicalTrials.gov</a></li></ul></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=(%22hyperactive%20deep%20tendon%20reflexes%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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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d4461084f3725e59a1ba2b">Hyperactive deep tendon reflexes</a>
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<div class="ralinkpop offscreen_noflow">Hyperactive deep tendon reflexes<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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