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<!--
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UID=893053
|
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ConceptID=C0240083
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormal joint morphology</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>893053</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.">C0240083</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Abnormal shape of joints; Abnormality of the joints; Anomaly of the joints; Joint disease</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0001367">HP:0001367</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">An abnormal structure or form of the joints, i.e., one or more of the articulations where two bones join. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Abnormal joint morphology</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/1763488" ref="tree=MeSH" title="MedGen record for Abnormality of the musculoskeletal system">Abnormality of the musculoskeletal system</a></span><ul><li><span class="TLline"><a href="/medgen/867418" ref="tree=MeSH" title="MedGen record for Abnormality of the skeletal system">Abnormality of the skeletal system</a></span><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="matched_ds">Abnormal joint morphology</span><ul><li><span class="TLline"><a href="/medgen/1841519" ref="tree=MeSH" title="MedGen record for Abnormal synovial membrane morphology">Abnormal synovial membrane morphology</a></span><ul><li><span class="TLline"><a href="/medgen/1841919" ref="tree=MeSH" title="MedGen record for Synovial granuloma">Synovial granuloma</a></span></li><li><span class="TLline"><a href="/medgen/140824" ref="tree=MeSH" title="MedGen record for Synovial lining hyperplasia">Synovial lining hyperplasia</a></span></li><li><span class="TLline"><a href="/medgen/21051" ref="tree=MeSH" title="MedGen record for Synovitis">Synovitis</a></span><ul><li><span class="TLline"><a href="/medgen/473482" ref="tree=MeSH" title="MedGen record for Acute Synovitis">Acute Synovitis</a></span></li><li><span class="TLline"><a href="/medgen/232927" ref="tree=MeSH" title="MedGen record for Tenosynovial giant cell tumor">Tenosynovial giant cell tumor</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/2043" ref="tree=MeSH" title="MedGen record for Arthritis">Arthritis</a></span><ul><li><span class="TLline"><a href="/medgen/116008" ref="tree=MeSH" title="MedGen record for Aggravated Arthritis">Aggravated Arthritis</a></span></li><li><span class="TLline"><a href="/medgen/57632" ref="tree=MeSH" title="MedGen record for Allergic arthritis">Allergic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/1375509" ref="tree=MeSH" title="MedGen record for Atrophic Arthritis">Atrophic Arthritis</a></span></li><li><span class="TLline"><a href="/medgen/120489" ref="tree=MeSH" title="MedGen record for Cervical osteoarthritis">Cervical osteoarthritis</a></span></li><li><span class="TLline"><a href="/medgen/154303" ref="tree=MeSH" title="MedGen record for Chondrocalcinosis">Chondrocalcinosis</a></span><ul><li><span class="TLline"><a href="/medgen/870801" ref="tree=MeSH" title="MedGen record for Polyarticular chondrocalcinosis">Polyarticular chondrocalcinosis</a></span></li><li><span class="TLline"><a href="/medgen/592677" ref="tree=MeSH" title="MedGen record for Rotator cuff tear arthropathy">Rotator cuff tear arthropathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/57851" ref="tree=MeSH" title="MedGen record for Climacteric arthritis">Climacteric arthritis</a></span></li><li><span class="TLline"><a href="/medgen/384947" ref="tree=MeSH" title="MedGen record for Destructive Arthritis">Destructive Arthritis</a></span></li><li><span class="TLline"><a href="/medgen/858875" ref="tree=MeSH" title="MedGen record for Early Inflammatory Arthritis">Early Inflammatory Arthritis</a></span></li><li><span class="TLline"><a href="/medgen/508755" ref="tree=MeSH" title="MedGen record for Enteropathic arthritis">Enteropathic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/42280" ref="tree=MeSH" title="MedGen record for Gout">Gout</a></span><ul><li><span 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of sacroiliac joint</a></span></li><li><span class="TLline"><a href="/medgen/215416" ref="tree=MeSH" title="MedGen record for Inflammatory spondylopathy">Inflammatory spondylopathy</a></span><ul><li><span class="TLline"><a href="/medgen/11561" ref="tree=MeSH" title="MedGen record for Ankylosing spondylitis">Ankylosing spondylitis</a></span></li><li><span class="TLline"><a href="/medgen/1784865" ref="tree=MeSH" title="MedGen record for Enteropathic Spondylitis">Enteropathic Spondylitis</a></span></li><li><span class="TLline"><a href="/medgen/592564" ref="tree=MeSH" title="MedGen record for Juvenile spondyloarthropathy">Juvenile spondyloarthropathy</a></span></li><li><span class="TLline"><a href="/medgen/389941" ref="tree=MeSH" title="MedGen record for Osteoarthritis, spine">Osteoarthritis, spine</a></span></li><li><span class="TLline"><a href="/medgen/181888" ref="tree=MeSH" title="MedGen record for Spondyloarthropathy">Spondyloarthropathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/760659" ref="tree=MeSH" title="MedGen record for Juvenile idiopathic arthritis">Juvenile idiopathic arthritis</a></span><ul><li><span class="TLline"><a href="/medgen/854059" ref="tree=MeSH" title="MedGen record for Enthesitis-related juvenile idiopathic arthritis">Enthesitis-related juvenile idiopathic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/443993" ref="tree=MeSH" title="MedGen record for Oligoarticular juvenile idiopathic arthritis">Oligoarticular juvenile idiopathic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/811463" ref="tree=MeSH" title="MedGen record for Psoriasis-related juvenile idiopathic arthritis">Psoriasis-related juvenile idiopathic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/855520" ref="tree=MeSH" title="MedGen record for Psoriatic Juvenile Idiopathic Arthritis">Psoriatic Juvenile Idiopathic Arthritis</a></span></li><li><span class="TLline"><a href="/medgen/855549" ref="tree=MeSH" title="MedGen record for Rheumatoid factor-negative juvenile idiopathic arthritis">Rheumatoid factor-negative juvenile idiopathic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/855737" ref="tree=MeSH" title="MedGen record for Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis">Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/730498" ref="tree=MeSH" title="MedGen record for Systemic onset juvenile chronic arthritis">Systemic onset juvenile chronic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/346934" ref="tree=MeSH" title="MedGen record for Systemic-onset juvenile idiopathic arthritis">Systemic-onset juvenile idiopathic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/856839" ref="tree=MeSH" title="MedGen record for Undifferentiated Juvenile Idiopathic Arthritis">Undifferentiated Juvenile Idiopathic Arthritis</a></span></li><li><span class="TLline"><a href="/medgen/1842681" ref="tree=MeSH" title="MedGen record for Unspecified juvenile idiopathic arthritis">Unspecified juvenile idiopathic arthritis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/66074" ref="tree=MeSH" title="MedGen record for Lyme arthritis">Lyme arthritis</a></span></li><li><span class="TLline"><a href="/medgen/536968" ref="tree=MeSH" title="MedGen record for Migratory arthritis">Migratory arthritis</a></span></li><li><span class="TLline"><a href="/medgen/857717" ref="tree=MeSH" title="MedGen record for Nonerosive Arthritis">Nonerosive Arthritis</a></span></li><li><span class="TLline"><a href="/medgen/856143" ref="tree=MeSH" title="MedGen record for Oligoarthritis">Oligoarthritis</a></span></li><li><span class="TLline"><a href="/medgen/45244" ref="tree=MeSH" title="MedGen record for Osteoarthritis">Osteoarthritis</a></span><ul><li><span class="TLline"><a href="/medgen/14530" ref="tree=MeSH" title="MedGen record for Osteoarthritis, hip">Osteoarthritis, hip</a></span></li><li><span class="TLline"><a href="/medgen/98371" ref="tree=MeSH" title="MedGen record for Osteoarthritis, knee">Osteoarthritis, knee</a></span></li><li><span class="TLline"><a href="/medgen/371977" ref="tree=MeSH" title="MedGen record for Premature osteoarthritis">Premature osteoarthritis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/45397" ref="tree=MeSH" title="MedGen record for Periarthritis">Periarthritis</a></span></li><li><span class="TLline"><a href="/medgen/56408" ref="tree=MeSH" title="MedGen record for Polyarticular arthritis">Polyarticular arthritis</a></span><ul><li><span class="TLline"><a href="/medgen/140816" ref="tree=MeSH" title="MedGen record for Juvenile chronic polyarthritis">Juvenile chronic polyarthritis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/712525" ref="tree=MeSH" title="MedGen record for Post-streptococcal reactive arthritis">Post-streptococcal reactive arthritis</a></span></li><li><span class="TLline"><a href="/medgen/19539" ref="tree=MeSH" title="MedGen record for Pseudogout">Pseudogout</a></span></li><li><span class="TLline"><a href="/medgen/2077" ref="tree=MeSH" title="MedGen record for Psoriatic arthritis">Psoriatic arthritis</a></span></li><li><span class="TLline"><a href="/medgen/48448" ref="tree=MeSH" title="MedGen record for Rheumatic Fever">Rheumatic Fever</a></span><ul><li><span class="TLline"><a href="/medgen/20565" ref="tree=MeSH" title="MedGen record for Rheumatic heart disease">Rheumatic heart disease</a></span></li><li><span class="TLline"><a href="/medgen/19780" ref="tree=MeSH" title="MedGen record for Rheumatic nodule">Rheumatic nodule</a></span></li><li><span class="TLline"><a href="/medgen/53087" ref="tree=MeSH" title="MedGen record for Wissler syndrome">Wissler syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/2078" ref="tree=MeSH" title="MedGen record for Rheumatoid arthritis">Rheumatoid arthritis</a></span><ul><li><span class="TLline"><a href="/medgen/39007" ref="tree=MeSH" title="MedGen record for Adult-onset Still disease">Adult-onset Still disease</a></span></li><li><span class="TLline"><a href="/medgen/743" ref="tree=MeSH" title="MedGen record for Caplan syndrome">Caplan syndrome</a></span></li><li><span class="TLline"><a href="/medgen/858872" ref="tree=MeSH" title="MedGen record for Early Rheumatoid Arthritis">Early Rheumatoid Arthritis</a></span></li><li><span class="TLline"><a href="/medgen/4674" ref="tree=MeSH" title="MedGen record for Felty syndrome">Felty syndrome</a></span></li><li><span class="TLline"><a href="/medgen/88662" ref="tree=MeSH" title="MedGen record for Juvenile onset Still disease">Juvenile onset Still disease</a></span></li><li><span class="TLline"><a href="/medgen/811462" ref="tree=MeSH" title="MedGen record for Juvenile rheumatoid arthritis">Juvenile rheumatoid arthritis</a></span></li><li><span class="TLline"><a href="/medgen/19781" ref="tree=MeSH" title="MedGen record for Rheumatoid nodule">Rheumatoid nodule</a></span></li><li><span class="TLline"><a href="/medgen/69122" ref="tree=MeSH" title="MedGen record for Rheumatoid vasculitis">Rheumatoid vasculitis</a></span></li><li><span class="TLline"><a href="/medgen/592547" ref="tree=MeSH" title="MedGen record for Seropositive rheumatoid arthritis">Seropositive rheumatoid arthritis</a></span></li><li><span class="TLline"><a href="/medgen/282890" ref="tree=MeSH" title="MedGen record for Sjogren syndrome">Sjogren syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1374751" ref="tree=MeSH" title="MedGen record for Sterile arthritis">Sterile arthritis</a></span></li><li><span class="TLline"><a href="/medgen/856092" ref="tree=MeSH" title="MedGen record for Suppurative arthritis">Suppurative arthritis</a></span></li><li><span class="TLline"><a href="/medgen/1788218" ref="tree=MeSH" title="MedGen record for Symmetric polyarthritis">Symmetric polyarthritis</a></span></li><li><span class="TLline"><a href="/medgen/672845" ref="tree=MeSH" title="MedGen record for Temporomandibular arthritis">Temporomandibular arthritis</a></span></li><li><span class="TLline"><a href="/medgen/1056641" ref="tree=MeSH" title="MedGen record for Wrist arthritis">Wrist arthritis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/7190" ref="tree=MeSH" title="MedGen record for Arthropathy">Arthropathy</a></span><ul><li><span class="TLline"><a href="/medgen/8101" ref="tree=MeSH" title="MedGen record for Ankylosis">Ankylosis</a></span><ul><li><span class="TLline"><a href="/medgen/870290" ref="tree=MeSH" title="MedGen record for Ankylosis of feet small joints">Ankylosis of feet small joints</a></span></li><li><span class="TLline"><a href="/medgen/923672" ref="tree=MeSH" title="MedGen record for Axial spondyloarthritis">Axial spondyloarthritis</a></span></li><li><span class="TLline"><a href="/medgen/592439" ref="tree=MeSH" title="MedGen record for Elbow ankylosis">Elbow ankylosis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/13917" ref="tree=MeSH" title="MedGen record for Arthralgia">Arthralgia</a></span><ul><li><span class="TLline"><a href="/medgen/870799" ref="tree=MeSH" title="MedGen record for Arthralgia/arthritis">Arthralgia/arthritis</a></span></li><li><span class="TLline"><a href="/medgen/11415" ref="tree=MeSH" title="MedGen record for Shoulder pain">Shoulder pain</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/2455" ref="tree=MeSH" title="MedGen record for Arthrogryposis">Arthrogryposis</a></span><ul><li><span class="TLline"><a href="/medgen/67391" ref="tree=MeSH" title="MedGen record for Congenital contractural arachnodactyly">Congenital contractural arachnodactyly</a></span></li><li><span class="TLline"><a href="/medgen/120516" ref="tree=MeSH" title="MedGen record for Freeman-Sheldon syndrome">Freeman-Sheldon syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/102354" ref="tree=MeSH" title="MedGen record for Behcet syndrome arthropathy">Behcet syndrome arthropathy</a></span></li><li><span class="TLline"><a href="/medgen/691" ref="tree=MeSH" title="MedGen record for Bursitis">Bursitis</a></span></li><li><span class="TLline"><a href="/medgen/508879" ref="tree=MeSH" title="MedGen record for Crystal arthropathy">Crystal arthropathy</a></span></li><li><span class="TLline"><a href="/medgen/445274" ref="tree=MeSH" title="MedGen record for Femoroacetabular impingement">Femoroacetabular impingement</a></span></li><li><span class="TLline"><a href="/medgen/75534" ref="tree=MeSH" title="MedGen record for Hallux rigidus">Hallux rigidus</a></span></li><li><span class="TLline"><a href="/medgen/222181" ref="tree=MeSH" title="MedGen record for Hydrarthrosis">Hydrarthrosis</a></span></li><li><span class="TLline"><a href="/medgen/5935" ref="tree=MeSH" title="MedGen record for Instability of joint">Instability of joint</a></span></li><li><span class="TLline"><a href="/medgen/41614" ref="tree=MeSH" title="MedGen record for Joint dislocation">Joint dislocation</a></span><ul><li><span class="TLline"><a href="/medgen/568603" ref="tree=MeSH" title="MedGen record for Diastasis of bone">Diastasis of bone</a></span></li><li><span class="TLline"><a href="/medgen/510527" ref="tree=MeSH" title="MedGen record for Diastasis of muscle">Diastasis of muscle</a></span></li><li><span class="TLline"><a href="/medgen/42455" ref="tree=MeSH" title="MedGen record for Hip dislocation">Hip dislocation</a></span></li><li><span class="TLline"><a href="/medgen/83065" ref="tree=MeSH" title="MedGen record for Joint subluxation">Joint subluxation</a></span></li><li><span class="TLline"><a href="/medgen/102364" ref="tree=MeSH" title="MedGen record for Knee dislocation">Knee dislocation</a></span></li><li><span class="TLline"><a href="/medgen/870803" ref="tree=MeSH" title="MedGen record for Large joint dislocations">Large joint dislocations</a></span></li><li><span class="TLline"><a href="/medgen/868125" ref="tree=MeSH" title="MedGen record for Lower extremity joint dislocation">Lower extremity joint dislocation</a></span></li><li><span class="TLline"><a href="/medgen/90698" ref="tree=MeSH" title="MedGen record for Multiple joint dislocation">Multiple joint dislocation</a></span></li><li><span class="TLline"><a href="/medgen/253896" ref="tree=MeSH" title="MedGen record for Patellar dislocation">Patellar dislocation</a></span></li><li><span class="TLline"><a href="/medgen/102355" ref="tree=MeSH" title="MedGen record for Pathological dislocation of joint">Pathological dislocation of joint</a></span></li><li><span class="TLline"><a href="/medgen/102356" ref="tree=MeSH" title="MedGen record for Recurrent joint dislocation">Recurrent joint dislocation</a></span></li><li><span class="TLline"><a href="/medgen/48655" ref="tree=MeSH" title="MedGen record for Shoulder dislocation">Shoulder dislocation</a></span></li><li><span class="TLline"><a href="/medgen/868126" ref="tree=MeSH" title="MedGen record for Upper extremity joint dislocation">Upper extremity joint dislocation</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/5479" ref="tree=MeSH" title="MedGen record for Joint hemorrhage">Joint hemorrhage</a></span></li><li><span class="TLline"><a href="/medgen/7191" ref="tree=MeSH" title="MedGen record for Loose body in joint">Loose body in joint</a></span></li><li><span class="TLline"><a href="/medgen/7575" ref="tree=MeSH" title="MedGen record for Metatarsalgia">Metatarsalgia</a></span><ul><li><span class="TLline"><a href="/medgen/90231" ref="tree=MeSH" title="MedGen record for Morton neuroma">Morton neuroma</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/3227" ref="tree=MeSH" title="MedGen record for Muscle contracture">Muscle contracture</a></span><ul><li><span class="TLline"><a href="/medgen/41672" ref="tree=MeSH" title="MedGen record for Contracture of palmar fascia">Contracture of palmar fascia</a></span></li><li><span class="TLline"><a href="/medgen/9257" ref="tree=MeSH" title="MedGen record for Contractures, Hip">Contractures, Hip</a></span></li><li><span class="TLline"><a href="/medgen/56385" ref="tree=MeSH" title="MedGen record for Plantar fibromatosis">Plantar fibromatosis</a></span></li><li><span class="TLline"><a href="/medgen/22684" ref="tree=MeSH" title="MedGen record for Volkmann contracture">Volkmann contracture</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10257" ref="tree=MeSH" title="MedGen record for Nail-patella syndrome">Nail-patella syndrome</a></span></li><li><span class="TLline"><a href="/medgen/13919" ref="tree=MeSH" title="MedGen record for Neuropathic arthropathy">Neuropathic arthropathy</a></span></li><li><span class="TLline"><a href="/medgen/18210" ref="tree=MeSH" title="MedGen record for Pachydermoperiostosis syndrome">Pachydermoperiostosis syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/1641972" ref="tree=MeSH" title="MedGen record for Hypertrophic osteoarthropathy, primary, autosomal recessive, 1">Hypertrophic osteoarthropathy, primary, autosomal recessive, 1</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/164080" ref="tree=MeSH" title="MedGen record for Patellofemoral pain syndrome">Patellofemoral pain syndrome</a></span></li><li><span class="TLline"><a href="/medgen/870782" ref="tree=MeSH" title="MedGen record for Polyarticular arthropathy">Polyarticular arthropathy</a></span></li><li><span class="TLline"><a href="/medgen/18211" ref="tree=MeSH" title="MedGen record for Secondary hypertrophic osteoarthropathy">Secondary hypertrophic osteoarthropathy</a></span></li><li><span class="TLline"><a href="/medgen/138249" ref="tree=MeSH" title="MedGen record for Shoulder impingement syndrome">Shoulder impingement syndrome</a></span></li><li><span class="TLline"><a href="/medgen/40275" ref="tree=MeSH" title="MedGen record for Synovial chondromatosis">Synovial chondromatosis</a></span></li><li><span class="TLline"><a href="/medgen/21092" ref="tree=MeSH" title="MedGen record for Temporomandibular joint disorder">Temporomandibular joint disorder</a></span><ul><li><span class="TLline"><a href="/medgen/21093" ref="tree=MeSH" title="MedGen record for Temporomandibular joint dysfunction syndrome">Temporomandibular joint dysfunction syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/101813" ref="tree=MeSH" title="MedGen record for Transient arthropathy">Transient arthropathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/347068" ref="tree=MeSH" title="MedGen record for Enlarged joints">Enlarged joints</a></span></li><li><span class="TLline"><a href="/medgen/56258" ref="tree=MeSH" title="MedGen record for Joint swelling">Joint swelling</a></span></li><li><span class="TLline"><a href="/medgen/1689016" ref="tree=MeSH" title="MedGen record for Periarticular soft-tissue mass">Periarticular soft-tissue mass</a></span></li><li><span class="TLline"><a href="/medgen/870786" ref="tree=MeSH" title="MedGen record for Progressive joint destruction">Progressive joint destruction</a></span></li><li><span class="TLline"><a href="/medgen/1842126" ref="tree=MeSH" title="MedGen record for Purulent synovial fluid">Purulent synovial fluid</a></span></li><li><span class="TLline"><a href="/medgen/606166" ref="tree=MeSH" title="MedGen record for Synovial fluid crystals">Synovial fluid crystals</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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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="divPopper rprt" id="rdis_78776"><div><strong>Laron-type isolated somatotropin defect</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>78776</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.">C0271568</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Laron syndrome is an autosomal recessive disorder characterized by marked short stature that results from failure to generate insulin-like growth factor I (IGF1; 147440) in response to growth hormone (GH; 139250). GH levels are normal or increased. The disorder is caused by dysfunction of the growth hormone receptor. A Laron syndrome-like phenotype associated with immunodeficiency (245590) is caused by a postreceptor defect, i.e., mutation in the STAT5B gene (604260). Patients with mutations in the GHR gene that cause only partial insensitivity to growth hormone have a form of short stature (604271).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/78776">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_98377"><div><strong>Metachondromatosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>98377</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.">C0410530</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Metachondromatosis is characterized by exostoses (osteochondromas), commonly of the hands and feet, and enchondromas of long bone metaphyses and iliac crests (summary by Sobreira et al., 2010).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/98377">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_224702"><div><strong>Progeroid short stature with pigmented nevi</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>224702</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.">C1261128</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Mulvihill-Smith syndrome is characterized by premature aging, multiple pigmented nevi, lack of facial subcutaneous fat, microcephaly, short stature, sensorineural hearing loss, and mental retardation. Immunodeficiency may also be a feature. Adult manifestations include the development of tumors, a sleep disorder with severe insomnia, and cognitive decline (summary by Yagihashi et al., 2009).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/224702">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_377706"><div><strong>Coracoclavicular joint, anomalous</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>377706</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.">C1852561</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/377706">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_349160"><div><strong>Bowen-Conradi syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>349160</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.">C1859405</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Bowen-Conradi syndrome (BWCNS) is an autosomal recessive disorder characterized by severely impaired prenatal and postnatal growth, microcephaly, prominent nose with absent glabellar angle, micrognathia, joint abnormalities including flexion contractures, camptodactyly, rocker-bottom feet, and severe psychomotor delay. Most patients do not survive beyond the first year of life as a result of complications associated with reduced mobility and failure to thrive (summary by Armistead et al., 2009).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/349160">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_355791"><div><strong>Spondyloarthropathy, susceptibility to, 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>355791</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.">C1866738</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/355791">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_477139"><div><strong>Multiple congenital anomalies-hypotonia-seizures syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>477139</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.">C3275508</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Multiple congenital anomalies-hypotonia-seizures syndrome-2 (MCAHS2) is an X-linked recessive neurodevelopmental disorder characterized by dysmorphic features, neonatal hypotonia, early-onset myoclonic seizures, and variable congenital anomalies involving the central nervous, cardiac, and urinary systems. Some affected individuals die in infancy (summary by Johnston et al., 2012). The phenotype shows clinical variability with regard to severity and extraneurologic features. However, most patients present in infancy with early-onset epileptic encephalopathy associated with developmental arrest and subsequent severe neurologic disability; these features are consistent with a form of developmental and epileptic encephalopathy (DEE) (summary by Belet et al., 2014, Kato et al., 2014). The disorder is caused by a defect in glycosylphosphatidylinositol (GPI) biosynthesis. For a discussion of genetic heterogeneity of MCAHS, see MCAHS1 (614080). For a discussion of nomenclature and genetic heterogeneity of DEE, see 308350. For a discussion of genetic heterogeneity of GPI biosynthesis defects, see GPIBD1 (610293).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/477139">Condition Record</a></div></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_349160" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Bowen-Conradi syndrome</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_377706" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Coracoclavicular joint, anomalous</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_78776" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Laron-type isolated somatotropin defect</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_98377" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Metachondromatosis</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_477139" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Multiple congenital anomalies-hypotonia-seizures syndrome 2</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_224702" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Progeroid short stature with pigmented nevi</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_355791" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondyloarthropathy, susceptibility to, 2</a></div></div>
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<div class="portlet mgSection" id="ID_105">
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<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/25822556">Diagnosis and treatment of temporomandibular disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gauer RL,
|
||
Semidey MJ</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2015 Mar 15;91(6):378-86.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25822556" target="_blank">25822556</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22149697">Evaluation and treatment of disorders of the infrapatellar fat pad.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dragoo JL,
|
||
Johnson C,
|
||
McConnell J</span><br />
|
||
<span class="medgenPMjournal">Sports Med</span>
|
||
2012 Jan 1;42(1):51-67.
|
||
doi: 10.2165/11595680-000000000-00000.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22149697" target="_blank">22149697</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20872595">2010 Rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aletaha D,
|
||
Neogi T,
|
||
Silman AJ,
|
||
Funovits J,
|
||
Felson DT,
|
||
Bingham CO 3rd,
|
||
Birnbaum NS,
|
||
Burmester GR,
|
||
Bykerk VP,
|
||
Cohen MD,
|
||
Combe B,
|
||
Costenbader KH,
|
||
Dougados M,
|
||
Emery P,
|
||
Ferraccioli G,
|
||
Hazes JM,
|
||
Hobbs K,
|
||
Huizinga TW,
|
||
Kavanaugh A,
|
||
Kay J,
|
||
Kvien TK,
|
||
Laing T,
|
||
Mease P,
|
||
Ménard HA,
|
||
Moreland LW,
|
||
Naden RL,
|
||
Pincus T,
|
||
Smolen JS,
|
||
Stanislawska-Biernat E,
|
||
Symmons D,
|
||
Tak PP,
|
||
Upchurch KS,
|
||
Vencovský J,
|
||
Wolfe F,
|
||
Hawker G</span><br />
|
||
<span class="medgenPMjournal">Arthritis Rheum</span>
|
||
2010 Sep;62(9):2569-81.
|
||
doi: 10.1002/art.27584.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20872595" target="_blank">20872595</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20joint%20morphology)%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 (417)</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/31431269">A pragmatic approach to prevent post-traumatic osteoarthritis after sport or exercise-related joint injury.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Whittaker JL,
|
||
Roos EM</span><br />
|
||
<span class="medgenPMjournal">Best Pract Res Clin Rheumatol</span>
|
||
2019 Feb;33(1):158-171.
|
||
Epub 2019 Mar 14
|
||
doi: 10.1016/j.berh.2019.02.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31431269" target="_blank">31431269</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30175856">Unravelling the hip pistol grip/cam deformity: Origins to joint degeneration.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Beaulé PE,
|
||
Grammatopoulos G,
|
||
Speirs A,
|
||
Geoffrey Ng KC,
|
||
Carsen S,
|
||
Frei H,
|
||
Melkus G,
|
||
Rakhra K,
|
||
Lamontagne M</span><br />
|
||
<span class="medgenPMjournal">J Orthop Res</span>
|
||
2018 Dec;36(12):3125-3135.
|
||
Epub 2018 Sep 21
|
||
doi: 10.1002/jor.24137.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30175856" target="_blank">30175856</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23123686">The hereditary predisposition to hip osteoarthritis and its association with abnormal joint morphology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pollard TC,
|
||
Batra RN,
|
||
Judge A,
|
||
Watkins B,
|
||
McNally EG,
|
||
Gill HS,
|
||
Thomas GE,
|
||
Glyn-Jones S,
|
||
Arden NK,
|
||
Carr AJ</span><br />
|
||
<span class="medgenPMjournal">Osteoarthritis Cartilage</span>
|
||
2013 Feb;21(2):314-21.
|
||
Epub 2012 Nov 1
|
||
doi: 10.1016/j.joca.2012.10.015.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23123686" target="_blank">23123686</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20130310">Genetic influences in the aetiology of femoroacetabular impingement: a sibling study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pollard TC,
|
||
Villar RN,
|
||
Norton MR,
|
||
Fern ED,
|
||
Williams MR,
|
||
Murray DW,
|
||
Carr AJ</span><br />
|
||
<span class="medgenPMjournal">J Bone Joint Surg Br</span>
|
||
2010 Feb;92(2):209-16.
|
||
doi: 10.1302/0301-620X.92B2.22850.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20130310" target="_blank">20130310</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20joint%20morphology%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 (4)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/20473125">Labrum: resection, repair and reconstruction sports medicine and arthroscopy review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Philippon MJ,
|
||
Schroder e Souza BG,
|
||
Briggs KK</span><br />
|
||
<span class="medgenPMjournal">Sports Med Arthrosc Rev</span>
|
||
2010 Jun;18(2):76-82.
|
||
doi: 10.1097/JSA.0b013e3181de376e.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20473125" target="_blank">20473125</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20joint%20morphology%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 (1)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/23123686">The hereditary predisposition to hip osteoarthritis and its association with abnormal joint morphology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pollard TC,
|
||
Batra RN,
|
||
Judge A,
|
||
Watkins B,
|
||
McNally EG,
|
||
Gill HS,
|
||
Thomas GE,
|
||
Glyn-Jones S,
|
||
Arden NK,
|
||
Carr AJ</span><br />
|
||
<span class="medgenPMjournal">Osteoarthritis Cartilage</span>
|
||
2013 Feb;21(2):314-21.
|
||
Epub 2012 Nov 1
|
||
doi: 10.1016/j.joca.2012.10.015.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23123686" target="_blank">23123686</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20joint%20morphology%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 (1)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/20130310">Genetic influences in the aetiology of femoroacetabular impingement: a sibling study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pollard TC,
|
||
Villar RN,
|
||
Norton MR,
|
||
Fern ED,
|
||
Williams MR,
|
||
Murray DW,
|
||
Carr AJ</span><br />
|
||
<span class="medgenPMjournal">J Bone Joint Surg Br</span>
|
||
2010 Feb;92(2):209-16.
|
||
doi: 10.1302/0301-620X.92B2.22850.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20130310" target="_blank">20130310</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19740213">The pathogenesis of osteoarthritis in cerebral palsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carter DR,
|
||
Tse B</span><br />
|
||
<span class="medgenPMjournal">Dev Med Child Neurol</span>
|
||
2009 Oct;51 Suppl 4:79-83.
|
||
doi: 10.1111/j.1469-8749.2009.03435.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19740213" target="_blank">19740213</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20joint%20morphology%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 (2)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
||
<div class="portlet mgSection" id="ID_113">
|
||
<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_content ln"><ul id="my-toc"></ul></div>
|
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</div>
|
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|
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<div class="portlet mgSection" id="ID_119">
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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>
|
||
<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Abnormal%20joint%20morphology" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_121">
|
||
<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>
|
||
<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20joint%20morphology)%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><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Abnormal%20joint%20morphology%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. 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>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_116">
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