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<!--
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UID=412568
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ConceptID=C2748518
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Lumbar scoliosis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>412568</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.">C2748518</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome; Finding; 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:0004626">HP:0004626</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 Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C2748518[DISCUI]&test_type=Clinical" ref="ncbi_uid=412568">C</a></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 Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=412568" ref="ncbi_uid=412568">V</a></span></span><span class="TLline">Lumbar scoliosis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/868760" ref="tree=MeSH" title="MedGen record for Abnormal skeletal morphology">Abnormal skeletal morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892434" ref="tree=MeSH" title="MedGen record for Abnormal axial skeleton morphology">Abnormal axial skeleton morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892426" ref="tree=MeSH" title="MedGen record for Abnormality of the vertebral column">Abnormality of the vertebral column</a></span><ul><li><span class="TLline"><a href="/medgen/869321" ref="tree=MeSH" title="MedGen record for Abnormal curvature of the vertebral column">Abnormal curvature of the vertebral column</a></span><ul><li><span class="TLline"><a href="/medgen/11348" ref="tree=MeSH" title="MedGen record for Scoliosis">Scoliosis</a></span><ul><li><span class="TLline"><a href="/medgen/196671" ref="tree=MeSH" title="MedGen record for Thoracolumbar scoliosis">Thoracolumbar scoliosis</a></span><ul><li><span class="matched_ds">Lumbar scoliosis</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">
|
||
<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_6009"><div><strong>Langer-Giedion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>6009</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.">C0023003</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Trichorhinophalangeal syndrome (TRPS) comprises TRPS I (caused by a heterozygous pathogenic variant in TRPS1) and TRPS II (caused by a contiguous gene deletion of TRPS1, RAD21, and EXT1). Both TRPS types are characterized by distinctive facial features (large nose with broad nasal ridge and tip and underdeveloped alae; thick and broad medial eyebrows; long philtrum; thin vermilion of the upper lip; and large prominent ears); ectodermal features (fine, sparse, depigmented, and slow-growing hair and dystrophic nails); and skeletal findings (short stature, brachydactyly with ulnar or radial deviation of the fingers, short feet, and early, marked hip dysplasia). TRPS II is additionally characterized by multiple osteochondromas and an increased risk of mild-to-moderate intellectual disability.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/6009">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_226942"><div><strong>Deficiency of hyaluronoglucosaminidase</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>226942</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.">C1291490</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Mucopolysaccharidosis type IX (MPS9) is a rare progressive lysosomal storage disorder caused by the deficiency of the enzyme hyaluronoglucosaminidase-1, which degrades hyaluronan (summary by Imundo et al., 2011).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/226942">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_373169"><div><strong>Arthrogryposis-severe scoliosis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>373169</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.">C1836756</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Distal arthrogryposis type 4 (DA4) is distinguished by the presence of scoliosis (summary by Bamshad et al., 2009). For a phenotypic description and a discussion of genetic heterogeneity of distal arthrogryposis, see DA1 (108120).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/373169">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_333031"><div><strong>CODAS syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>333031</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.">C1838180</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CODAS is an acronym for cerebral, ocular, dental, auricular, and skeletal anomalies. CODAS syndrome is a rare disorder characterized by a distinctive constellation of features that includes developmental delay, craniofacial anomalies, cataracts, ptosis, median nasal groove, delayed tooth eruption, hearing loss, short stature, delayed epiphyseal ossification, metaphyseal hip dysplasia, and vertebral coronal clefts (summary by Strauss et al., 2015).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/333031">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_435914"><div><strong>Mucolipidosis type II</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>435914</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.">C2673377</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">GNPTAB-related disorders comprise the phenotypes mucolipidosis II (ML II) and mucolipidosis IIIa/ß (ML IIIa/ß), and phenotypes intermediate between ML II and ML IIIa/ß. ML II is evident at birth and slowly progressive; death most often occurs in early childhood. Orthopedic abnormalities present at birth may include thoracic deformity, kyphosis, clubfeet, deformed long bones, and/or dislocation of the hip(s). Growth often ceases in the second year of life; contractures develop in all large joints. The skin is thickened, facial features are coarse, and gingiva are hypertrophic. All children have cardiac involvement, most commonly thickening and insufficiency of the mitral valve and, less frequently, the aortic valve. Progressive mucosal thickening narrows the airways, and gradual stiffening of the thoracic cage contributes to respiratory insufficiency, the most common cause of death. ML IIIa/ß becomes evident at about age three years with slow growth rate and short stature; joint stiffness and pain initially in the shoulders, hips, and fingers; gradual mild coarsening of facial features; and normal to mildly impaired cognitive development. Pain from osteoporosis becomes more severe during adolescence. Cardiorespiratory complications (restrictive lung disease, thickening and insufficiency of the mitral and aortic valves, left and/or right ventricular hypertrophy) are common causes of death, typically in early to middle adulthood. Phenotypes intermediate between ML II and ML IIIa/ß are characterized by physical growth in infancy that resembles that of ML II and neuromotor and speech development that resemble that of ML IIIa/ß.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/435914">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_411234"><div><strong>Spondyloepimetaphyseal dysplasia, PAPSS2 type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>411234</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.">C2748515</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">This form of brachyolmia, here designated brachyolmia type 4, is characterized by short-trunk stature with normal intelligence and facies. The radiographic features include rectangular vertebral bodies with irregular endplates and narrow intervertebral discs, precocious calcification of rib cartilages, short femoral neck, mildly shortened metacarpals, and mild epiphyseal and metaphyseal changes of the tubular bones (summary by Miyake et al., 2012).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/411234">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766784"><div><strong>Seckel syndrome 7</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766784</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.">C3553870</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Microcephalic primordial dwarfism, Dauber type is a rare, genetic developmental defect during embryogenesis characterized by severe pre- and postnatal growth retardation, severe microcephaly, severe developmental delay and intelletual disability, severe adult short stature and facial dysmorphism (incl. hypotelorism, small ears, prominent nose). Other reported features include skeletal anomalies (Madelung deformity, clinodactyly, mild lumbar scoliosis, bilateral hip dysplasia) and seizures. Absence of thelarche and menarche is also associated.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766784">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_863825"><div><strong>Microcephaly and chorioretinopathy 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>863825</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.">C4015388</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Microcephaly and chorioretinopathy-2 is an autosomal recessive developmental disorder characterized by delayed psychomotor development, visual impairment, and short stature (summary by Martin et al., 2014). For a discussion of genetic heterogeneity of microcephaly and chorioretinopathy, see MCCRP1 (251270).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/863825">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1392054"><div><strong>Intellectual disability, X-linked, syndromic, 35</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1392054</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.">C4478383</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/1392054">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1615839"><div><strong>Intellectual disability, autosomal dominant 52</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1615839</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.">C4540478</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1615839">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794204"><div><strong>Usmani-Riazuddin syndrome, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794204</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.">C5561994</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive Usmani-Riazzudin syndrome (USRISR) is a neurodevelopmental disorder characterized by global developmental delay with impaired intellectual development and speech delay, hypotonia, spasticity, and behavioral abnormalities, most commonly aggressive behavior. More variable additional features may include seizures, scoliosis, and joint laxity (Usmani et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794204">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1840948"><div><strong>Leukodystrophy, hypomyelinating, 26, with chondrodysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1840948</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.">C5830312</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypomyelinating leukodystrophy-26 with chondrodysplasia (HLD26) is characterized by severe psychomotor delay, predominantly involving motor and expressive language development, with cerebral and cerebellar atrophy and corpus callosum hypoplasia. In addition, patients show pre- and postnatal growth retardation, early-onset scoliosis, and dislocations of large joints (Guasto et al., 2022). For a general phenotypic description and a discussion of genetic heterogeneity of HLD, see HLD1 (312080).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1840948">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_373169" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Arthrogryposis-severe scoliosis syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_333031" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">CODAS syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_226942" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Deficiency of hyaluronoglucosaminidase</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1615839" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, autosomal dominant 52</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1392054" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, X-linked, syndromic, 35</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (12)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_6009" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Langer-Giedion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1840948" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Leukodystrophy, hypomyelinating, 26, with chondrodysplasia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_863825" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Microcephaly and chorioretinopathy 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_435914" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucolipidosis type II</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766784" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Seckel syndrome 7</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_411234" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondyloepimetaphyseal dysplasia, PAPSS2 type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794204" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Usmani-Riazuddin syndrome, autosomal recessive</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/37437804">A New Objective Radiographic Criteria for Diagnosis of Adult Idiopathic Scoliosis: Apical Pedicle Diameter Asymmetry.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lin JD,
|
||
Schupper AJ,
|
||
Matthew J,
|
||
Lee N,
|
||
Osorio JA,
|
||
Marciano G,
|
||
Lombardi JM,
|
||
Sardar Z,
|
||
Lehman RA,
|
||
Lenke LG</span><br />
|
||
<span class="medgenPMjournal">World Neurosurg</span>
|
||
2023 Oct;178:e141-e146.
|
||
Epub 2023 Jul 10
|
||
doi: 10.1016/j.wneu.2023.07.010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37437804" target="_blank">37437804</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29412187">How does sagittal imbalance affect the appropriateness of surgical indications and selection of procedure in the treatment of degenerative scoliosis? Findings from the RAND/UCLA Appropriate Use Criteria study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Daubs MD,
|
||
Brara HS,
|
||
Raaen LB,
|
||
Chen PG,
|
||
Anderson AT,
|
||
Asch SM,
|
||
Nuckols TK</span><br />
|
||
<span class="medgenPMjournal">Spine J</span>
|
||
2018 May;18(5):900-911.
|
||
Epub 2018 Feb 2
|
||
doi: 10.1016/j.spinee.2018.01.027.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29412187" target="_blank">29412187</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26679874">Surgery for Degenerative Lumbar Scoliosis: The Development of Appropriateness Criteria.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen PG,
|
||
Daubs MD,
|
||
Berven S,
|
||
Raaen LB,
|
||
Anderson AT,
|
||
Asch SM,
|
||
Nuckols TK;
|
||
Degenerative Lumbar Scoliosis Appropriateness Group</span><br />
|
||
<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
|
||
2016 May;41(10):910-8.
|
||
doi: 10.1097/BRS.0000000000001392.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26679874" target="_blank">26679874</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22lumbar%20scoliosis%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 (14)</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/37774911">How to manage a ureteral injury after anterior lumbar spine interbody fusion surgery.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leroy HA,
|
||
De Buck P,
|
||
Marcq G,
|
||
Assaker R</span><br />
|
||
<span class="medgenPMjournal">Neurochirurgie</span>
|
||
2023 Nov;69(6):101503.
|
||
Epub 2023 Sep 27
|
||
doi: 10.1016/j.neuchi.2023.101503.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37774911" target="_blank">37774911</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35351065">The classification of coronal deformity based on preoperative global coronal malalignment for adult spinal deformity is questionable.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang J,
|
||
Yu Y,
|
||
Gao S,
|
||
Hai Y,
|
||
Wu B,
|
||
Su X,
|
||
Wang Z</span><br />
|
||
<span class="medgenPMjournal">BMC Musculoskelet Disord</span>
|
||
2022 Mar 29;23(1):300.
|
||
doi: 10.1186/s12891-022-05246-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35351065" target="_blank">35351065</a><a href="/pmc/articles/PMC8962466" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28598493">Adult Degenerative Lumbar Scoliosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wong E,
|
||
Altaf F,
|
||
Oh LJ,
|
||
Gray RJ</span><br />
|
||
<span class="medgenPMjournal">Orthopedics</span>
|
||
2017 Nov 1;40(6):e930-e939.
|
||
Epub 2017 Jun 9
|
||
doi: 10.3928/01477447-20170606-02.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28598493" target="_blank">28598493</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28594511">Adult Lumbar Scoliosis: Nonsurgical Versus Surgical Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Falakassa J,
|
||
Hu SS</span><br />
|
||
<span class="medgenPMjournal">Instr Course Lect</span>
|
||
2017 Feb 15;66:353-360.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28594511" target="_blank">28594511</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27544679">Lumbar scoliosis associated with spinal stenosis in idiopathic and degenerative cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Le Huec JC,
|
||
Cogniet A,
|
||
Mazas S,
|
||
Faundez A</span><br />
|
||
<span class="medgenPMjournal">Eur J Orthop Surg Traumatol</span>
|
||
2016 Oct;26(7):705-12.
|
||
Epub 2016 Aug 20
|
||
doi: 10.1007/s00590-016-1829-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27544679" target="_blank">27544679</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Lumbar%20scoliosis%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 (407)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37774911">How to manage a ureteral injury after anterior lumbar spine interbody fusion surgery.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leroy HA,
|
||
De Buck P,
|
||
Marcq G,
|
||
Assaker R</span><br />
|
||
<span class="medgenPMjournal">Neurochirurgie</span>
|
||
2023 Nov;69(6):101503.
|
||
Epub 2023 Sep 27
|
||
doi: 10.1016/j.neuchi.2023.101503.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37774911" target="_blank">37774911</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29747234">Laparoscopic nephrectomy in a patient with severe scoliosis: A case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tamura D,
|
||
Ito A,
|
||
Kikuchi D,
|
||
Tsuyukubo T,
|
||
Kato R,
|
||
Kato Y,
|
||
Konari S,
|
||
Omori S,
|
||
Obara W</span><br />
|
||
<span class="medgenPMjournal">Asian J Endosc Surg</span>
|
||
2019 Jan;12(1):122-124.
|
||
Epub 2018 May 10
|
||
doi: 10.1111/ases.12597.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29747234" target="_blank">29747234</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28598493">Adult Degenerative Lumbar Scoliosis.</a></div>
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<span class="bold">PMID: </span><a href="/pubmed/28598493" target="_blank">28598493</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/26679874">Surgery for Degenerative Lumbar Scoliosis: The Development of Appropriateness Criteria.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Chen PG,
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Daubs MD,
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Raaen LB,
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Asch SM,
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Nuckols TK;
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<div class="nl"><a target="_blank" href="/pubmed/12602636">Adult degenerative lumbar scoliosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Daffner SD,
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<div class="nl"><a target="_blank" href="/pubmed/37774911">How to manage a ureteral injury after anterior lumbar spine interbody fusion surgery.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Leroy HA,
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<span class="bold">PMID: </span><a href="/pubmed/37774911" target="_blank">37774911</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Lumbar%20scoliosis%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 (139)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/29747234">Laparoscopic nephrectomy in a patient with severe scoliosis: A case report.</a></div>
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Ito A,
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<span class="bold">PMID: </span><a href="/pubmed/29747234" target="_blank">29747234</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28598493">Adult Degenerative Lumbar Scoliosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wong E,
|
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Altaf F,
|
||
Oh LJ,
|
||
Gray RJ</span><br />
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<span class="medgenPMjournal">Orthopedics</span>
|
||
2017 Nov 1;40(6):e930-e939.
|
||
Epub 2017 Jun 9
|
||
doi: 10.3928/01477447-20170606-02.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28598493" target="_blank">28598493</a></div>
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||
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<div class="nl"><a target="_blank" href="/pubmed/27489322">Morphology and Prevalence Study of Lumbar Scoliosis in 7,075 Multiracial Asian Adults.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Liu G,
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Tan JH,
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Ee G,
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Chan YH,
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Low SL,
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<div class="nl"><a target="_blank" href="/pubmed/27220970">De novo degenerative lumbar scoliosis: a systematic review of prognostic factors for curve progression.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Faraj SS,
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Holewijn RM,
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van Hooff ML,
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de Kleuver M,
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Pellisé F,
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Haanstra TM</span><br />
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<span class="medgenPMjournal">Eur Spine J</span>
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2016 Aug;25(8):2347-58.
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Epub 2016 May 24
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||
<span class="bold">PMID: </span><a href="/pubmed/27220970" target="_blank">27220970</a></div>
|
||
|
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<div class="nl"><a target="_blank" href="/pubmed/6635787">The effect of the Milwaukee brace on spinal decompensation in idiopathic scoliosis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Rudicel S,
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<span class="bold">PMID: </span><a href="/pubmed/6635787" target="_blank">6635787</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Lumbar%20scoliosis%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 (173)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37179281">Biomechanical modeling and assessment of lumbar vertebral body tethering configurations.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Martin S,
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<span class="bold">PMID: </span><a href="/pubmed/37179281" target="_blank">37179281</a></div>
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||
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||
<div class="nl"><a target="_blank" href="/pubmed/36933036">Treatment of degenerative lumbar scoliosis using transforaminal lumbar interbody fusion based on the concept of intervertebral correction.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Lai J,
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Tan H,
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Feng H,
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Lan Z,
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Sun Z,
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Wang J,
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Fu Y,
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He S</span><br />
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<span class="medgenPMjournal">Int Orthop</span>
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2023 May;47(5):1303-1313.
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<span class="bold">PMID: </span><a href="/pubmed/36933036" target="_blank">36933036</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/36509364">Malpractice litigation after spinal surgery: A review of allegations in France in 1990-2020.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Rougereau G,
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Marty-Diloy T,
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Bonaccorsi R,
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Vialle R,
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Boisrenoult P,
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Pascal-Moussellard H,
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Langlais T</span><br />
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2023 Apr;109(2):103510.
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<span class="bold">PMID: </span><a href="/pubmed/36509364" target="_blank">36509364</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/35428916">The impact of lumbar alignment targets on mechanical complications after adult lumbar scoliosis surgery.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Dial BL,
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Hills JM,
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Smith JS,
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Sardi JP,
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Lazaro B,
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Shaffrey CI,
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Bess S,
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Schwab FJ,
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Lafage V,
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Lafage R,
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Kelly MP,
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Bridwell KH</span><br />
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<span class="medgenPMjournal">Eur Spine J</span>
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<span class="bold">PMID: </span><a href="/pubmed/35428916" target="_blank">35428916</a></div>
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||
|
||
<div class="nl"><a target="_blank" href="/pubmed/6635787">The effect of the Milwaukee brace on spinal decompensation in idiopathic scoliosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rudicel S,
|
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Renshaw TS</span><br />
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<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
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1983 May-Jun;8(4):385-7.
|
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doi: 10.1097/00007632-198305000-00008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/6635787" target="_blank">6635787</a></div>
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||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Lumbar%20scoliosis%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 (253)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<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/37228067">Prevalence of osteoporosis in spinal surgery patients older than 50 years: A systematic review and meta-analysis.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Fan ZQ,
|
||
Yan XA,
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||
Li BF,
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||
Shen E,
|
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Xu X,
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||
Wang H,
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Zhuang Y</span><br />
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<span class="medgenPMjournal">PLoS One</span>
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||
2023;18(5):e0286110.
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||
Epub 2023 May 25
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||
doi: 10.1371/journal.pone.0286110.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37228067" target="_blank">37228067</a><a href="/pmc/articles/PMC10212156" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29178306">Outcomes of Short Fusion versus Long Fusion for Adult Degenerative Scoliosis: A Systematic Review and Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Phan K,
|
||
Xu J,
|
||
Maharaj MM,
|
||
Li J,
|
||
Kim JS,
|
||
Di Capua J,
|
||
Somani S,
|
||
Tan KA,
|
||
Mobbs RJ,
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||
Cho SK</span><br />
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<span class="medgenPMjournal">Orthop Surg</span>
|
||
2017 Nov;9(4):342-349.
|
||
doi: 10.1111/os.12357.
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||
<span class="bold">PMID: </span><a href="/pubmed/29178306" target="_blank">29178306</a><a href="/pmc/articles/PMC6584300" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27220970">De novo degenerative lumbar scoliosis: a systematic review of prognostic factors for curve progression.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Faraj SS,
|
||
Holewijn RM,
|
||
van Hooff ML,
|
||
de Kleuver M,
|
||
Pellisé F,
|
||
Haanstra TM</span><br />
|
||
<span class="medgenPMjournal">Eur Spine J</span>
|
||
2016 Aug;25(8):2347-58.
|
||
Epub 2016 May 24
|
||
doi: 10.1007/s00586-016-4619-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27220970" target="_blank">27220970</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26679874">Surgery for Degenerative Lumbar Scoliosis: The Development of Appropriateness Criteria.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen PG,
|
||
Daubs MD,
|
||
Berven S,
|
||
Raaen LB,
|
||
Anderson AT,
|
||
Asch SM,
|
||
Nuckols TK;
|
||
Degenerative Lumbar Scoliosis Appropriateness Group</span><br />
|
||
<span class="medgenPMjournal">Spine (Phila Pa 1976)</span>
|
||
2016 May;41(10):910-8.
|
||
doi: 10.1097/BRS.0000000000001392.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26679874" target="_blank">26679874</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20718168">Correction with instrumented fusion versus non-corrective surgery for degenerative lumbar scoliosis: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Prommahachai A,
|
||
Wittayapirot K,
|
||
Jirarattanaphochai K,
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Sae-Jung S</span><br />
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<span class="medgenPMjournal">J Med Assoc Thai</span>
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||
2010 Aug;93(8):920-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20718168" target="_blank">20718168</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Lumbar%20scoliosis%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 (5)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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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>
|
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|
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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="Genetic_Testing_Registry">Genetic Testing Registry</h1><a sid="106" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C2748518%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (3)</a></li>
|
||
<li><a href="/gtr/tests?term=C2748518%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (3)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C2748518%5bDISCUI%5d" target="_blank">See all (3)</a></total></li>
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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=Lumbar%20scoliosis" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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