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<!--
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||
UID=167271
|
||
ConceptID=C0852866
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Cervical cord compression</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>167271</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.">C0852866</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Cervical cord compression myelopathy</td></tr>
|
||
<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:0002341">HP:0002341</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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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">Compression of the spinal cord in the cervical region, generally manifested by paresthesias and numbness, weakness, difficulty walking, abnormalities of coordination, and neck pain or stiffness. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Cervical cord compression</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/868416" ref="tree=MeSH" title="MedGen record for Abnormal nervous system morphology">Abnormal nervous system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892343" ref="tree=MeSH" title="MedGen record for Morphological central nervous system abnormality">Morphological central nervous system abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/892345" ref="tree=MeSH" title="MedGen record for Abnormal spinal cord morphology">Abnormal spinal cord morphology</a></span><ul><li><span class="TLline"><a href="/medgen/11549" ref="tree=MeSH" title="MedGen record for Spinal cord compression">Spinal cord compression</a></span><ul><li><span class="matched_ds">Cervical cord compression</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">
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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_7734"><div><strong>Mucopolysaccharidosis, MPS-II</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>7734</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.">C0026705</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Mucopolysaccharidosis type II (MPS II; also known as Hunter syndrome) is an X-linked multisystem disorder characterized by glycosaminoglycan (GAG) accumulation. The vast majority of affected individuals are male; on rare occasion heterozygous females manifest findings. Age of onset, disease severity, and rate of progression vary significantly among affected males. In those with the neuronopathic phenotype, central nervous system (CNS) involvement (manifesting primarily as progressive cognitive deterioration), progressive airway disease, and cardiac disease usually results in death in the first or second decade of life. In those with the non-neuronopathic phenotype, the CNS is minimally or not affected. However, the effect of GAG accumulation on other organ systems can be severe. Survival into the early adult years with normal intelligence is common in the non-neuronopathic phenotype. Additional findings in neuronopathic and non-neuronopathic MPS II include: short stature, macrocephaly with or without communicating hydrocephalus, macroglossia, hoarse voice, conductive and sensorineural hearing loss, dysostosis multiplex, spinal stenosis, carpal tunnel syndrome, and hepatosplenomegaly.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/7734">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_6453"><div><strong>Mucopolysaccharidosis, MPS-I-S</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>6453</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.">C0026708</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Mucopolysaccharidosis type I (MPS I) is a progressive multisystem disorder with features ranging over a continuum of severity. While affected individuals have traditionally been classified as having one of three MPS I syndromes (Hurler syndrome, Hurler-Scheie syndrome, or Scheie syndrome), no easily measurable biochemical differences have been identified and the clinical findings overlap. Affected individuals are best described as having either a phenotype consistent with either severe (Hurler syndrome) or attenuated MPS I, a distinction that influences therapeutic options. Severe MPS I: Infants appear normal at birth. Typical early manifestations are nonspecific (e.g., umbilical or inguinal hernia, frequent upper respiratory tract infections before age 1 year). Coarsening of the facial features may not become apparent until after age one year. Gibbus deformity of the lower spine is common and often noted within the first year. Progressive skeletal dysplasia (dysostosis multiplex) involving all bones is universal, as is progressive arthropathy involving most joints. By age three years, linear growth decreases. Intellectual disability is progressive and profound but may not be readily apparent in the first year of life. Progressive cardiorespiratory involvement, hearing loss, and corneal clouding are common. Without treatment, death (typically from cardiorespiratory failure) usually occurs within the first ten years of life. Attenuated MPS I: Clinical onset is usually between ages three and ten years. The severity and rate of disease progression range from serious life-threatening complications leading to death in the second to third decade, to a normal life span complicated by significant disability from progressive joint manifestations and cardiorespiratory disease. While some individuals have no neurologic involvement and psychomotor development may be normal in early childhood, learning disabilities and psychiatric manifestations can be present later in life. Hearing loss, cardiac valvular disease, respiratory involvement, and corneal clouding are common.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/6453">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_75551"><div><strong>Marshall-Smith syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75551</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.">C0265211</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The Marshall-Smith syndrome (MRSHSS) is a malformation syndrome characterized by accelerated skeletal maturation, relative failure to thrive, respiratory difficulties, mental retardation, and unusual facies, including prominent forehead, shallow orbits, blue sclerae, depressed nasal bridge, and micrognathia (Adam et al., 2005).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75551">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_98378"><div><strong>Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>98378</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:">C0410538</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">COMP-related pseudoachondroplasia (COMP-PSACH) is characterized by normal length at birth and normal facies. Often the presenting feature is a waddling gait, recognized at the onset of walking. Typically, the growth rate falls below the standard growth curve by approximately age two years, leading to a moderately severe form of disproportionate short-limb short stature. Joint pain during childhood, particularly in the large joints of the lower extremities, is common. Degenerative joint disease is progressive; approximately 50% of individuals with COMP-PSACH eventually require hip replacement surgery.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/98378">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1638106"><div><strong>Anauxetic dysplasia 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1638106</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.">C4551965</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The cartilage-hair hypoplasia – anauxetic dysplasia (CHH-AD) spectrum disorders are a continuum that includes the following phenotypes: Metaphyseal dysplasia without hypotrichosis (MDWH). Cartilage-hair hypoplasia (CHH). Anauxetic dysplasia (AD). CHH-AD spectrum disorders are characterized by severe disproportionate (short-limb) short stature that is usually recognized in the newborn, and occasionally prenatally because of the short extremities. Other findings include joint hypermobility, fine, silky hair, immunodeficiency, anemia, increased risk for malignancy, gastrointestinal dysfunction, and impaired spermatogenesis. The most severe phenotype, AD, has the most pronounced skeletal phenotype, may be associated with atlantoaxial subluxation in the newborn, and may include cognitive deficiency. The clinical manifestations of the CHH-AD spectrum disorders are variable, even within the same family.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1638106">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1638106" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Anauxetic dysplasia 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75551" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Marshall-Smith syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_6453" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis, MPS-I-S</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_7734" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis, MPS-II</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_98378" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29173427">Management of the Patient with Cervical Cord Compression but no Evidence of Myelopathy: What Should We do?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Naito K,
|
||
Yamagata T,
|
||
Ohata K,
|
||
Takami T</span><br />
|
||
<span class="medgenPMjournal">Neurosurg Clin N Am</span>
|
||
2018 Jan;29(1):145-152.
|
||
Epub 2017 Oct 27
|
||
doi: 10.1016/j.nec.2017.09.010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29173427" target="_blank">29173427</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25036872">Management of asymptomatic cervical spinal stenosis in the setting of symptomatic tandem lumbar stenosis: a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ghobrial GM,
|
||
Oppenlander ME,
|
||
Maulucci CM,
|
||
Viereck M,
|
||
Prasad S,
|
||
Sharan AD,
|
||
Harrop JS</span><br />
|
||
<span class="medgenPMjournal">Clin Neurol Neurosurg</span>
|
||
2014 Sep;124:114-8.
|
||
Epub 2014 Jul 2
|
||
doi: 10.1016/j.clineuro.2014.06.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25036872" target="_blank">25036872</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22938833">A multinational, multidisciplinary consensus for the diagnosis and management of spinal cord compression among patients with mucopolysaccharidosis VI.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Solanki GA,
|
||
Alden TD,
|
||
Burton BK,
|
||
Giugliani R,
|
||
Horovitz DD,
|
||
Jones SA,
|
||
Lampe C,
|
||
Martin KW,
|
||
Ryan ME,
|
||
Schaefer MK,
|
||
Siddiqui A,
|
||
White KK,
|
||
Harmatz P</span><br />
|
||
<span class="medgenPMjournal">Mol Genet Metab</span>
|
||
2012 Sep;107(1-2):15-24.
|
||
Epub 2012 Jul 21
|
||
doi: 10.1016/j.ymgme.2012.07.018.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22938833" target="_blank">22938833</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22cervical%20cord%20compression%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 (7)</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/34287724">Higher incidence of cervical spinal cord compression in amyotrophic lateral sclerosis: a single-institute cohort study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsuzono K,
|
||
Suzuki M,
|
||
Miura K,
|
||
Ozawa T,
|
||
Mashiko T,
|
||
Koide R,
|
||
Tanaka R,
|
||
Fujimoto S</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2022 Feb;43(2):1079-1086.
|
||
Epub 2021 Jul 21
|
||
doi: 10.1007/s10072-021-05465-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34287724" target="_blank">34287724</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29173427">Management of the Patient with Cervical Cord Compression but no Evidence of Myelopathy: What Should We do?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Naito K,
|
||
Yamagata T,
|
||
Ohata K,
|
||
Takami T</span><br />
|
||
<span class="medgenPMjournal">Neurosurg Clin N Am</span>
|
||
2018 Jan;29(1):145-152.
|
||
Epub 2017 Oct 27
|
||
doi: 10.1016/j.nec.2017.09.010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29173427" target="_blank">29173427</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24878549">Monoparesis of upper extremity due to ipsilateral upper cervical cord compression: report of two cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kawaguchi Y,
|
||
Yasuda T,
|
||
Seki S,
|
||
Hori T,
|
||
Nakano M,
|
||
Kimura T</span><br />
|
||
<span class="medgenPMjournal">J Orthop Sci</span>
|
||
2015 Sep;20(5):939-42.
|
||
Epub 2014 May 31
|
||
doi: 10.1007/s00776-014-0588-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24878549" target="_blank">24878549</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23700231">Risk factors for development of myelopathy in patients with cervical spondylotic cord compression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsunaga S,
|
||
Komiya S,
|
||
Toyama Y</span><br />
|
||
<span class="medgenPMjournal">Eur Spine J</span>
|
||
2015 Apr;24 Suppl 2:142-9.
|
||
Epub 2013 May 23
|
||
doi: 10.1007/s00586-013-2839-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23700231" target="_blank">23700231</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23316777">Quadriplegia in a child following adenotonsillectomy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agarwal J,
|
||
Tandon MS,
|
||
Singh D,
|
||
Ganjoo P</span><br />
|
||
<span class="medgenPMjournal">Anaesthesia</span>
|
||
2013 May;68(5):523-6.
|
||
Epub 2013 Jan 14
|
||
doi: 10.1111/anae.12118.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23316777" target="_blank">23316777</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20cord%20compression%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 (93)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30249680">Clinical Reasoning: A 58-year-old woman with systemic scleroderma and progressive cervical cord compression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Karschnia P,
|
||
Fulbright RK,
|
||
Laurans MS,
|
||
Huttner AJ,
|
||
Baehring JM</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2018 Sep 25;91(13):e1262-e1264.
|
||
doi: 10.1212/WNL.0000000000006242.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30249680" target="_blank">30249680</a><a href="/pmc/articles/PMC6161549" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20385007">Mucopolysaccharidosis VI.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Valayannopoulos V,
|
||
Nicely H,
|
||
Harmatz P,
|
||
Turbeville S</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2010 Apr 12;5:5.
|
||
doi: 10.1186/1750-1172-5-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20385007" target="_blank">20385007</a><a href="/pmc/articles/PMC2873242" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18328977">Achondroplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baujat G,
|
||
Legeai-Mallet L,
|
||
Finidori G,
|
||
Cormier-Daire V,
|
||
Le Merrer M</span><br />
|
||
<span class="medgenPMjournal">Best Pract Res Clin Rheumatol</span>
|
||
2008 Mar;22(1):3-18.
|
||
doi: 10.1016/j.berh.2007.12.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18328977" target="_blank">18328977</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9246353">Quadriplegia with cervical cord compression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tammam A,
|
||
Crockard HA</span><br />
|
||
<span class="medgenPMjournal">Postgrad Med J</span>
|
||
1997 Jun;73(860):381-2.
|
||
doi: 10.1136/pgmj.73.860.381.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9246353" target="_blank">9246353</a><a href="/pmc/articles/PMC2431347" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8915062">Tophaceous pseudogout.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rivera-Sanfeliz G,
|
||
Resnick D,
|
||
Haghighi P,
|
||
Wong W,
|
||
Lanier T</span><br />
|
||
<span class="medgenPMjournal">Skeletal Radiol</span>
|
||
1996 Oct;25(7):699-701.
|
||
doi: 10.1007/s002560050164.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8915062" target="_blank">8915062</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20cord%20compression%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 (149)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36763843">Deep Learning Algorithm for Identifying Cervical Cord Compression Due to Degenerative Canal Stenosis on Radiography.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tamai K,
|
||
Terai H,
|
||
Hoshino M,
|
||
Tabuchi H,
|
||
Kato M,
|
||
Toyoda H,
|
||
Suzuki A,
|
||
Takahashi S,
|
||
Yabu A,
|
||
Sawada Y,
|
||
Iwamae M,
|
||
Oka M,
|
||
Nakaniwa K,
|
||
Okada M,
|
||
Nakamura H</span><br />
|
||
<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
|
||
2023 Apr 15;48(8):519-525.
|
||
Epub 2023 Feb 10
|
||
doi: 10.1097/BRS.0000000000004595.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36763843" target="_blank">36763843</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24846845">Spontaneous resolution of cervical cord compression induced by hydrogel (Duraseal).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rustagi T,
|
||
Lavelle WF</span><br />
|
||
<span class="medgenPMjournal">Spine J</span>
|
||
2014 Oct 1;14(10):2511-2.
|
||
Epub 2014 May 16
|
||
doi: 10.1016/j.spinee.2014.05.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24846845" target="_blank">24846845</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23316777">Quadriplegia in a child following adenotonsillectomy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agarwal J,
|
||
Tandon MS,
|
||
Singh D,
|
||
Ganjoo P</span><br />
|
||
<span class="medgenPMjournal">Anaesthesia</span>
|
||
2013 May;68(5):523-6.
|
||
Epub 2013 Jan 14
|
||
doi: 10.1111/anae.12118.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23316777" target="_blank">23316777</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10633472">Extraskeletal problems and amyloid.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Drüeke TB</span><br />
|
||
<span class="medgenPMjournal">Kidney Int Suppl</span>
|
||
1999 Dec;73:S89-93.
|
||
doi: 10.1046/j.1523-1755.1999.07315.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10633472" target="_blank">10633472</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7572300">Cervical cord compression in diffuse idiopathic skeletal hyperostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Martínez-Berenguer L,
|
||
Gómez-Calcerrada D,
|
||
Martínez-López JJ</span><br />
|
||
<span class="medgenPMjournal">J Am Board Fam Pract</span>
|
||
1995 Jul-Aug;8(4):331-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7572300" target="_blank">7572300</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20cord%20compression%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 (38)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34287724">Higher incidence of cervical spinal cord compression in amyotrophic lateral sclerosis: a single-institute cohort study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsuzono K,
|
||
Suzuki M,
|
||
Miura K,
|
||
Ozawa T,
|
||
Mashiko T,
|
||
Koide R,
|
||
Tanaka R,
|
||
Fujimoto S</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2022 Feb;43(2):1079-1086.
|
||
Epub 2021 Jul 21
|
||
doi: 10.1007/s10072-021-05465-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34287724" target="_blank">34287724</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33764392">Tophaceous gout: an unusual cause of cervical cord compression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Park EH,
|
||
Yoo WH,
|
||
Choi Y</span><br />
|
||
<span class="medgenPMjournal">Rheumatology (Oxford)</span>
|
||
2021 Dec 24;61(1):467.
|
||
doi: 10.1093/rheumatology/keab301.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33764392" target="_blank">33764392</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29173427">Management of the Patient with Cervical Cord Compression but no Evidence of Myelopathy: What Should We do?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Naito K,
|
||
Yamagata T,
|
||
Ohata K,
|
||
Takami T</span><br />
|
||
<span class="medgenPMjournal">Neurosurg Clin N Am</span>
|
||
2018 Jan;29(1):145-152.
|
||
Epub 2017 Oct 27
|
||
doi: 10.1016/j.nec.2017.09.010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29173427" target="_blank">29173427</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23700231">Risk factors for development of myelopathy in patients with cervical spondylotic cord compression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsunaga S,
|
||
Komiya S,
|
||
Toyama Y</span><br />
|
||
<span class="medgenPMjournal">Eur Spine J</span>
|
||
2015 Apr;24 Suppl 2:142-9.
|
||
Epub 2013 May 23
|
||
doi: 10.1007/s00586-013-2839-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23700231" target="_blank">23700231</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20385007">Mucopolysaccharidosis VI.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Valayannopoulos V,
|
||
Nicely H,
|
||
Harmatz P,
|
||
Turbeville S</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2010 Apr 12;5:5.
|
||
doi: 10.1186/1750-1172-5-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20385007" target="_blank">20385007</a><a href="/pmc/articles/PMC2873242" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20cord%20compression%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 (63)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30830044">Prevalence and Predictive Factors of Concurrent Cervical Spinal Cord Compression in Adult Spinal Deformity.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shimizu T,
|
||
Lehman RA Jr,
|
||
Pongmanee S,
|
||
Alex Sielatycki J,
|
||
Leung E,
|
||
Riew KD,
|
||
Lenke LG</span><br />
|
||
<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
|
||
2019 Aug 1;44(15):1049-1056.
|
||
doi: 10.1097/BRS.0000000000003007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30830044" target="_blank">30830044</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28948090">Predictors of symptomatic myelopathy in degenerative cervical spinal cord compression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kadanka Z Jr,
|
||
Adamova B,
|
||
Kerkovsky M,
|
||
Kadanka Z,
|
||
Dusek L,
|
||
Jurova B,
|
||
Vlckova E,
|
||
Bednarik J</span><br />
|
||
<span class="medgenPMjournal">Brain Behav</span>
|
||
2017 Sep;7(9):e00797.
|
||
Epub 2017 Aug 11
|
||
doi: 10.1002/brb3.797.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28948090" target="_blank">28948090</a><a href="/pmc/articles/PMC5607559" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27815654">Musculoskeletal manifestations of primary hyperparathyroidism.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pappu R,
|
||
Jabbour SA,
|
||
Reginato AM,
|
||
Reginato AJ</span><br />
|
||
<span class="medgenPMjournal">Clin Rheumatol</span>
|
||
2016 Dec;35(12):3081-3087.
|
||
Epub 2016 Nov 4
|
||
doi: 10.1007/s10067-016-3450-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27815654" target="_blank">27815654</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23700231">Risk factors for development of myelopathy in patients with cervical spondylotic cord compression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Matsunaga S,
|
||
Komiya S,
|
||
Toyama Y</span><br />
|
||
<span class="medgenPMjournal">Eur Spine J</span>
|
||
2015 Apr;24 Suppl 2:142-9.
|
||
Epub 2013 May 23
|
||
doi: 10.1007/s00586-013-2839-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23700231" target="_blank">23700231</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23665161">Review of clinical presentation and diagnosis of mucopolysaccharidosis IVA.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hendriksz CJ,
|
||
Harmatz P,
|
||
Beck M,
|
||
Jones S,
|
||
Wood T,
|
||
Lachman R,
|
||
Gravance CG,
|
||
Orii T,
|
||
Tomatsu S</span><br />
|
||
<span class="medgenPMjournal">Mol Genet Metab</span>
|
||
2013 Sep-Oct;110(1-2):54-64.
|
||
Epub 2013 Apr 10
|
||
doi: 10.1016/j.ymgme.2013.04.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23665161" target="_blank">23665161</a><a href="/pmc/articles/PMC3755102" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20cord%20compression%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 (76)</a></div></div>
|
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</div>
|
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|
||
<div class="portlet mgSection" id="ID_104">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/23963006">Nonoperative management of cervical myelopathy: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rhee JM,
|
||
Shamji MF,
|
||
Erwin WM,
|
||
Bransford RJ,
|
||
Yoon ST,
|
||
Smith JS,
|
||
Kim HJ,
|
||
Ely CG,
|
||
Dettori JR,
|
||
Patel AA,
|
||
Kalsi-Ryan S</span><br />
|
||
<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
|
||
2013 Oct 15;38(22 Suppl 1):S55-67.
|
||
doi: 10.1097/BRS.0b013e3182a7f41d.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23963006" target="_blank">23963006</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19736557">Brain death and the cervical spinal cord: a confounding factor for the clinical examination.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Joffe AR,
|
||
Anton N,
|
||
Blackwood J</span><br />
|
||
<span class="medgenPMjournal">Spinal Cord</span>
|
||
2010 Jan;48(1):2-9.
|
||
Epub 2009 Sep 8
|
||
doi: 10.1038/sc.2009.115.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19736557" target="_blank">19736557</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cervical%20cord%20compression%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (2)</a></div></div>
|
||
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|
||
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<div class="supplemental col three_col last">
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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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=(%22cervical%20cord%20compression%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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