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<meta name="keywords" content="C1328407, acetabular dysplasia, anatomical abnormality, decreased femoral head coverage by acetabulum, dysplasia, hip, dysplasias, hip, dysplastic acetabulae, finding, hip dysplasia, hip dysplasias, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="A smaller than normal acetabulum that has insufficient femoral head coverage leading to abnormal hip joint contact pressures, instability and pain." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Acetabular dysplasia (Concept Id: C1328407)
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<!--
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||
UID=233069
|
||
ConceptID=C1328407
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Acetabular dysplasia</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>233069</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C1328407</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Dysplasia, Hip; Dysplasias, Hip; Hip Dysplasia; Hip Dysplasias</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:0008807">HP:0008807</a></td></tr>
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</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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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>
|
||
<div class="portlet_content ln">A smaller than normal acetabulum that has insufficient femoral head coverage leading to abnormal hip joint contact pressures, instability and pain. [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>
|
||
<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="TLline">Acetabular dysplasia</span><ul><li class="TLclosed"><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 Ocolor" title="OMIM"><a ref="ncbi_uid=1640560" target="_blank" href="/omim/142700">O</a></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=1640560" ref="ncbi_uid=1640560">V</a></span></span><span class="TLline"><a href="/medgen/1640560" ref="tree=GTR&ncbi_uid=1640560&link_uid=1640560" title="View MedGen record for 'Developmental dysplasia of the hip'">Developmental dysplasia of the hip</a></span></li></ul></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/536898" ref="tree=MeSH" title="MedGen record for Abnormality of limbs">Abnormality of limbs</a></span><ul><li><span class="TLline"><a href="/medgen/242750" ref="tree=MeSH" title="MedGen record for Abnormality of the lower limb">Abnormality of the lower limb</a></span><ul><li><span class="TLline"><a href="/medgen/866624" ref="tree=MeSH" title="MedGen record for Abnormality of lower limb joint">Abnormality of lower limb joint</a></span><ul><li><span class="TLline"><a href="/medgen/866552" ref="tree=MeSH" title="MedGen record for Abnormal hip joint morphology">Abnormal hip joint morphology</a></span><ul><li><span class="TLline"><a href="/medgen/867374" ref="tree=MeSH" title="MedGen record for Abnormal acetabulum morphology">Abnormal acetabulum morphology</a></span><ul><li><span class="matched_ds">Acetabular dysplasia</span><ul><li><span class="TLline"><a href="/medgen/1640560" ref="tree=MeSH" title="MedGen record for Developmental dysplasia of the hip">Developmental dysplasia of the hip</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
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||
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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>
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||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_43108"><div><strong>Mucopolysaccharidosis type 7</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>43108</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.">C0085132</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Individuals with mucopolysaccharidosis type VII (MPS VII) can present perinatally with early demise, nonimmune hydrops fetalis, cholestatic jaundice, and hepatosplenomegaly, or in early childhood with developmental delay and characteristic musculoskeletal features (e.g., short neck, short-trunk short stature, pectus deformity, gibbus, and joint stiffness/contractures) and craniofacial features (e.g., macrocephaly, coarse hair, coarse facies, corneal clouding, and macroglossia). Skeletal survey shows features of dysostosis multiplex including thickened cortical bone, abnormal J-shaped sella turcica, paddle- or oar-shaped ribs, short, thickened clavicles, platyspondyly with anterior beaking of the lower thoracic and lumbar vertebrae, and proximal pointing of the metacarpals and metatarsals. Complications include developmental delay, intellectual disability, hepatosplenomegaly, spinal stenosis, recurrent otitis media, hearing loss, pulmonary disease, obstructive sleep apnea, hernias, feeding difficulties, and heart valve disease.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/43108">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_82696"><div><strong>Autosomal recessive multiple pterygium syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>82696</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.">C0265261</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Multiple pterygium syndromes comprise a group of multiple congenital anomaly disorders characterized by webbing (pterygia) of the neck, elbows, and/or knees and joint contractures (arthrogryposis) (Morgan et al., 2006). The multiple pterygium syndromes are phenotypically and genetically heterogeneous but are traditionally divided into prenatally lethal (253290) and nonlethal (Escobar) types.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/82696">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_266288"><div><strong>Developmental dysplasia of the hip 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>266288</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.">C1306065</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/266288">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_374912"><div><strong>Hermansky-Pudlak syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>374912</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.">C1842362</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hermansky-Pudlak syndrome (HPS) is characterized by oculocutaneous albinism, a bleeding diathesis, and, in some individuals, pulmonary fibrosis, granulomatous colitis, and/or immunodeficiency. Ocular findings include nystagmus, reduced iris pigment, reduced retinal pigment, foveal hypoplasia with significant reduction in visual acuity (usually in the range of 20/50 to 20/400), and strabismus in many individuals. Hair color ranges from white to brown; skin color ranges from white to olive and is usually at least a shade lighter than that of other family members. The bleeding diathesis can result in variable degrees of bruising, epistaxis, gingival bleeding, postpartum hemorrhage, colonic bleeding, and prolonged bleeding with menses or after tooth extraction, circumcision, and/or other surgeries. Pulmonary fibrosis, colitis, and/or neutropenia have been reported in individuals with pathogenic variants in some HPS-related genes. Pulmonary fibrosis, a restrictive lung disease, typically causes symptoms in the early 30s and can progress to death within a decade. Granulomatous colitis is severe in about 15% of affected individuals. Neutropenia and/or immune defects occur primarily in individuals with pathogenic variants in AP3B1 and AP3D1.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/374912">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_336581"><div><strong>Richieri Costa-Pereira syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>336581</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.">C1849348</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Patients with Richieri-Costa-Pereira syndrome display a pattern of anomalies consisting of microstomia, micrognathia, abnormal fusion of the mandible, cleft palate/Robin sequence, absence of lower central incisors, minor ear anomalies, hypoplastic first ray, abnormal tibiae, hypoplastic halluces, and clubfeet. Learning disability is also a common finding (summary by Favaro et al., 2011).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/336581">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_462230"><div><strong>Familial clubfoot due to 17q23.1q23.2 microduplication</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>462230</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.">C3150880</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">17q23.1-q23.2 microduplication is a newly described cause of familial isolated clubfoot.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/462230">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_481368"><div><strong>Hereditary spastic paraplegia 47</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>481368</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.">C3279738</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">AP-4-associated hereditary spastic paraplegia (AP-4-HSP) is a childhood-onset and complex form of hereditary spastic paraplegia. Spastic paraparesis is a universal feature in affected individuals. Manifestations typically begin before age one year, with infants presenting with hypotonia, mild postnatal microcephaly, and delayed developmental milestones. Seizures are common in early childhood, often starting as prolonged febrile seizures. As the disease progresses, older children have intellectual disability that is usually moderate to severe; most affected individuals communicate nonverbally. Neurobehavioral/psychiatric manifestations (e.g., impulsivity, hyperactivity, and inattention) are common. Hypotonia transitions to progressive lower-extremity weakness and spasticity, accompanied by pyramidal signs such as plantar extension, ankle clonus, and hyperreflexia. Although some children achieve independent ambulation, most eventually lose this ability and rely on mobility aids or wheelchairs. In adolescence or early adulthood, spasticity may affect the upper extremities in some individuals but is generally less severe and not significantly disabling. Complications in some individuals include contractures, foot deformities, and bladder and bowel dysfunction. Dysphagia may emerge in advanced stages of the disease.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/481368">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_816016"><div><strong>Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>816016</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.">C3809686</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CTCF-related disorder is characterized by developmental delay / intellectual disability (ranging from mild to severe), with both speech and motor delays being common; feeding difficulties, including dysphagia, and other gastrointestinal issues (gastroesophageal reflux disease and/or irritable bowel syndrome) that can lead to growth deficiency; hypotonia; eye anomalies (strabismus and/or refractive errors); scoliosis; nonspecific dysmorphic features; sleep disturbance; tooth anomalies (crowded teeth and/or abnormal decay); and, less commonly, other congenital anomalies (cleft palate, gastrointestinal malrotation, genitourinary anomalies, and congenital heart defects, including aortic ectasia). Short stature, seizures, hearing loss, recurrent infections, microcephaly, and autistic features have also been described in a minority of affected individuals. At least four reported individuals with CTCF-related disorder developed Wilms tumor, one of whom had bilateral Wilms tumor. However, there is no clear evidence of a significant predisposition for the development of cancer in individuals with CTCF-related disorder at this time.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/816016">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_816240"><div><strong>Autism spectrum disorder - epilepsy - arthrogryposis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>816240</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.">C3809910</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Arthrogryposis, impaired intellectual development, and seizures (AMRS) is an autosomal recessive disorder characterized by skeletal abnormalities, including arthrogryposis, short limbs, and vertebral malformations, impaired intellectual development, and seizures consistent with early-onset epileptic encephalopathy in some patients. Other features may include cleft palate, micrognathia, posterior embryotoxon, talipes valgus, rocker-bottom feet, and dysmorphic facies (Edmondson et al., 2017; Marini et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/816240">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_894399"><div><strong>Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>894399</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.">C4225285</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Klippel-Feil syndrome-4 with nemaline myopathy and facial dysmorphism (KFS4) is an autosomal recessive disorder characterized mainly by severe hypotonia apparent from infancy. Klippel-Feil anomaly is primarily defined by fusion of the cervical spine, with associated low posterior hairline and limited neck mobility being observed in about half of patients (summary by Alazami et al., 2015). For a general description and a discussion of genetic heterogeneity of Klippel-Feil syndrome, see KFS1 (118100).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/894399">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_903483"><div><strong>Acrofacial dysostosis Cincinnati type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>903483</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.">C4225317</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The Cincinnati type of acrofacial dysostosis is a ribosomopathy characterized by a spectrum of mandibulofacial dysostosis phenotypes, with or without extrafacial skeletal defects (Weaver et al., 2015). In addition, a significant number of neurologic abnormalities have been reported, ranging from mild delays to refractory epilepsy, as well as an increased incidence of congenital heart defects, primarily septal in nature (Smallwood et al., 2023).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/903483">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934594"><div><strong>Mucopolysaccharidosis-plus syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934594</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.">C4310627</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">MPSPS is an autosomal recessive inborn error of metabolism resulting in a multisystem disorder with features of the mucopolysaccharidosis lysosomal storage diseases (see, e.g., 607016). Patients present in infancy or early childhood with respiratory difficulties, cardiac problems, anemia, dysostosis multiplex, renal involvement, coarse facies, and delayed psychomotor development. Most patients die of cardiorespiratory failure in the first years of life (summary by Kondo et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934594">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1632008"><div><strong>Acrofrontofacionasal dysostosis 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1632008</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.">C4551987</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/1632008">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1674961"><div><strong>Diamond-Blackfan anemia 20</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1674961</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.">C5193022</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Diamond-Blackfan anemia (DBA) is characterized by a profound normochromic and usually macrocytic anemia with normal leukocytes and platelets, congenital malformations in up to 50%, and growth deficiency in 30% of affected individuals. The hematologic complications occur in 90% of affected individuals during the first year of life. The phenotypic spectrum ranges from a mild form (e.g., mild anemia or no anemia with only subtle erythroid abnormalities, physical malformations without anemia) to a severe form of fetal anemia resulting in nonimmune hydrops fetalis. DBA is associated with an increased risk for acute myelogenous leukemia (AML), myelodysplastic syndrome (MDS), and solid tumors including osteogenic sarcoma.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1674961">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1718250"><div><strong>Combined oxidative phosphorylation deficiency 43</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1718250</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.">C5394284</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/1718250">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1803456"><div><strong>Neurodevelopmental disorder with neuromuscular and skeletal abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1803456</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.">C5676965</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with neuromuscular and skeletal abnormalities (NEDNMS) is an autosomal recessive disorder characterized by global developmental delay apparent from infancy or early childhood. The severity of the disorder is highly variable. Affected individuals show impaired intellectual development and motor delay associated with either severe hypotonia or hypertonia and spasticity. Most affected individuals have skeletal defects and dysmorphic facial features. Some may have ocular or auditory problems, peripheral neuropathy, behavioral abnormalities, and nonspecific findings on brain imaging (Kurolap et al., 2022).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1803456">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_903483" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acrofacial dysostosis Cincinnati type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1632008" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acrofrontofacionasal dysostosis 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_816240" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autism spectrum disorder - epilepsy - arthrogryposis syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_82696" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive multiple pterygium syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1718250" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Combined oxidative phosphorylation deficiency 43</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (16)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_266288" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental dysplasia of the hip 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1674961" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Diamond-Blackfan anemia 20</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_462230" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Familial clubfoot due to 17q23.1q23.2 microduplication</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_481368" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hereditary spastic paraplegia 47</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_374912" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hermansky-Pudlak syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_816016" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_894399" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_43108" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis type 7</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934594" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis-plus syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1803456" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with neuromuscular and skeletal abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_336581" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Richieri Costa-Pereira syndrome</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31959678">Consensus recommendations on the classification, definition and diagnostic criteria of hip-related pain in young and middle-aged active adults from the International Hip-related Pain Research Network, Zurich 2018.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Reiman MP,
|
||
Agricola R,
|
||
Kemp JL,
|
||
Heerey JJ,
|
||
Weir A,
|
||
van Klij P,
|
||
Kassarjian A,
|
||
Mosler AB,
|
||
Ageberg E,
|
||
Hölmich P,
|
||
Warholm KM,
|
||
Griffin D,
|
||
Mayes S,
|
||
Khan KM,
|
||
Crossley KM,
|
||
Bizzini M,
|
||
Bloom N,
|
||
Casartelli NC,
|
||
Diamond LE,
|
||
Di Stasi S,
|
||
Drew M,
|
||
Friedman DJ,
|
||
Freke M,
|
||
Gojanovic B,
|
||
Glyn-Jones S,
|
||
Harris-Hayes M,
|
||
Hunt MA,
|
||
Impellizzeri FM,
|
||
Ishøi L,
|
||
Jones DM,
|
||
King MG,
|
||
Lawrenson PR,
|
||
Leunig M,
|
||
Lewis CL,
|
||
Mathieu N,
|
||
Moksnes H,
|
||
Risberg MA,
|
||
Scholes MJ,
|
||
Semciw AI,
|
||
Serner A,
|
||
Thorborg K,
|
||
Wörner T,
|
||
Dijkstra HP</span><br />
|
||
<span class="medgenPMjournal">Br J Sports Med</span>
|
||
2020 Jun;54(11):631-641.
|
||
Epub 2020 Jan 20
|
||
doi: 10.1136/bjsports-2019-101453.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31959678" target="_blank">31959678</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25439013">Evaluation and treatment of developmental hip dysplasia in the newborn and infant.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schwend RM,
|
||
Shaw BA,
|
||
Segal LS</span><br />
|
||
<span class="medgenPMjournal">Pediatr Clin North Am</span>
|
||
2014 Dec;61(6):1095-107.
|
||
Epub 2014 Sep 18
|
||
doi: 10.1016/j.pcl.2014.08.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25439013" target="_blank">25439013</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15972928">Acetabular dysplasia after treatment for developmental dysplasia of the hip.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ibrahim S</span><br />
|
||
<span class="medgenPMjournal">J Bone Joint Surg Br</span>
|
||
2005 Jul;87(7):1025; author reply 1025.
|
||
doi: 10.1302/0301-620X.87B7.16662.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15972928" target="_blank">15972928</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22acetabular%20dysplasia%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 (53)</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/33673886">Hip Dysplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harris JD,
|
||
Lewis BD,
|
||
Park KJ</span><br />
|
||
<span class="medgenPMjournal">Clin Sports Med</span>
|
||
2021 Apr;40(2):271-288.
|
||
Epub 2021 Jan 19
|
||
doi: 10.1016/j.csm.2020.11.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33673886" target="_blank">33673886</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32436427">Sclerotic lesions of the femoral head-neck junction for diagnosis of femoroacetabular impingement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hananouchi T,
|
||
Aoki SK</span><br />
|
||
<span class="medgenPMjournal">J Orthop Surg (Hong Kong)</span>
|
||
2020 Jan-Apr;28(2):2309499020924161.
|
||
doi: 10.1177/2309499020924161.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32436427" target="_blank">32436427</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12198462">Natural history of hips with borderline acetabular index and acetabular dysplasia in infants.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mladenov K,
|
||
Dora C,
|
||
Wicart P,
|
||
Seringe R</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Orthop</span>
|
||
2002 Sep-Oct;22(5):607-12.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12198462" target="_blank">12198462</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11730331">Developmental dysplasia of the hip from six months to four years of age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vitale MG,
|
||
Skaggs DL</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Orthop Surg</span>
|
||
2001 Nov-Dec;9(6):401-11.
|
||
doi: 10.5435/00124635-200111000-00005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11730331" target="_blank">11730331</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8370774">Triple innominate osteotomy for acetabular dysplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Faciszewski T,
|
||
Coleman SS,
|
||
Biddulph G</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Orthop</span>
|
||
1993 Jul-Aug;13(4):426-30.
|
||
doi: 10.1097/01241398-199307000-00002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8370774" target="_blank">8370774</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acetabular%20dysplasia%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 (727)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31959678">Consensus recommendations on the classification, definition and diagnostic criteria of hip-related pain in young and middle-aged active adults from the International Hip-related Pain Research Network, Zurich 2018.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Reiman MP,
|
||
Agricola R,
|
||
Kemp JL,
|
||
Heerey JJ,
|
||
Weir A,
|
||
van Klij P,
|
||
Kassarjian A,
|
||
Mosler AB,
|
||
Ageberg E,
|
||
Hölmich P,
|
||
Warholm KM,
|
||
Griffin D,
|
||
Mayes S,
|
||
Khan KM,
|
||
Crossley KM,
|
||
Bizzini M,
|
||
Bloom N,
|
||
Casartelli NC,
|
||
Diamond LE,
|
||
Di Stasi S,
|
||
Drew M,
|
||
Friedman DJ,
|
||
Freke M,
|
||
Gojanovic B,
|
||
Glyn-Jones S,
|
||
Harris-Hayes M,
|
||
Hunt MA,
|
||
Impellizzeri FM,
|
||
Ishøi L,
|
||
Jones DM,
|
||
King MG,
|
||
Lawrenson PR,
|
||
Leunig M,
|
||
Lewis CL,
|
||
Mathieu N,
|
||
Moksnes H,
|
||
Risberg MA,
|
||
Scholes MJ,
|
||
Semciw AI,
|
||
Serner A,
|
||
Thorborg K,
|
||
Wörner T,
|
||
Dijkstra HP</span><br />
|
||
<span class="medgenPMjournal">Br J Sports Med</span>
|
||
2020 Jun;54(11):631-641.
|
||
Epub 2020 Jan 20
|
||
doi: 10.1136/bjsports-2019-101453.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31959678" target="_blank">31959678</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30271085">Novel methionyl-tRNA synthetase gene variants/phenotypes in interstitial lung and liver disease: A case report and review of literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Abuduxikuer K,
|
||
Feng JY,
|
||
Lu Y,
|
||
Xie XB,
|
||
Chen L,
|
||
Wang JS</span><br />
|
||
<span class="medgenPMjournal">World J Gastroenterol</span>
|
||
2018 Sep 28;24(36):4208-4216.
|
||
doi: 10.3748/wjg.v24.i36.4208.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30271085" target="_blank">30271085</a><a href="/pmc/articles/PMC6158480" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28566387">Acetabular dysplasia: multiple pathologies and myriad solutions.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Witt JD,
|
||
Haddad FS</span><br />
|
||
<span class="medgenPMjournal">Bone Joint J</span>
|
||
2017 Jun;99-B(6):705-707.
|
||
doi: 10.1302/0301-620X.99B6.BJJ-2017-0491.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28566387" target="_blank">28566387</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27343395">Hip Instability: Current Concepts and Treatment Options.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dumont GD</span><br />
|
||
<span class="medgenPMjournal">Clin Sports Med</span>
|
||
2016 Jul;35(3):435-447.
|
||
Epub 2016 Apr 20
|
||
doi: 10.1016/j.csm.2016.02.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27343395" target="_blank">27343395</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11730331">Developmental dysplasia of the hip from six months to four years of age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vitale MG,
|
||
Skaggs DL</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Orthop Surg</span>
|
||
2001 Nov-Dec;9(6):401-11.
|
||
doi: 10.5435/00124635-200111000-00005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11730331" target="_blank">11730331</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acetabular%20dysplasia%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 (309)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28567213">Rotational Acetabular Osteotomy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yasunaga Y,
|
||
Fujii J,
|
||
Tanaka R,
|
||
Yasuhara S,
|
||
Yamasaki T,
|
||
Adachi N,
|
||
Ochi M</span><br />
|
||
<span class="medgenPMjournal">Clin Orthop Surg</span>
|
||
2017 Jun;9(2):129-135.
|
||
Epub 2017 May 8
|
||
doi: 10.4055/cios.2017.9.2.129.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28567213" target="_blank">28567213</a><a href="/pmc/articles/PMC5435649" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28566390">The Birmingham Interlocking Pelvic Osteotomy for acetabular dysplasia: 13- to 21-year survival outcomes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mei-Dan O,
|
||
Jewell D,
|
||
Garabekyan T,
|
||
Brockwell J,
|
||
Young DA,
|
||
McBryde CW,
|
||
O'Hara JN</span><br />
|
||
<span class="medgenPMjournal">Bone Joint J</span>
|
||
2017 Jun;99-B(6):724-731.
|
||
doi: 10.1302/0301-620X.99B6.BJJ-2016-0198.R3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28566390" target="_blank">28566390</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24460107">Incomplete periacetabular acetabuloplasty.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carsi B,
|
||
Al-Hallao S,
|
||
Wahed K,
|
||
Page J,
|
||
Clarke NM</span><br />
|
||
<span class="medgenPMjournal">Acta Orthop</span>
|
||
2014 Feb;85(1):66-70.
|
||
Epub 2014 Jan 24
|
||
doi: 10.3109/17453674.2014.886030.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24460107" target="_blank">24460107</a><a href="/pmc/articles/PMC3940994" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23452416">Acetabular fractures in children: a review of the literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gänsslen A,
|
||
Hildebrand F,
|
||
Heidari N,
|
||
Weinberg AM</span><br />
|
||
<span class="medgenPMjournal">Acta Chir Orthop Traumatol Cech</span>
|
||
2013;80(1):10-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23452416" target="_blank">23452416</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11433159">Use of allografts in Pemberton osteotomies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kessler JI,
|
||
Stevens PM,
|
||
Smith JT,
|
||
Carroll KL</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Orthop</span>
|
||
2001 Jul-Aug;21(4):468-73.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11433159" target="_blank">11433159</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acetabular%20dysplasia%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 (169)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31959678">Consensus recommendations on the classification, definition and diagnostic criteria of hip-related pain in young and middle-aged active adults from the International Hip-related Pain Research Network, Zurich 2018.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Reiman MP,
|
||
Agricola R,
|
||
Kemp JL,
|
||
Heerey JJ,
|
||
Weir A,
|
||
van Klij P,
|
||
Kassarjian A,
|
||
Mosler AB,
|
||
Ageberg E,
|
||
Hölmich P,
|
||
Warholm KM,
|
||
Griffin D,
|
||
Mayes S,
|
||
Khan KM,
|
||
Crossley KM,
|
||
Bizzini M,
|
||
Bloom N,
|
||
Casartelli NC,
|
||
Diamond LE,
|
||
Di Stasi S,
|
||
Drew M,
|
||
Friedman DJ,
|
||
Freke M,
|
||
Gojanovic B,
|
||
Glyn-Jones S,
|
||
Harris-Hayes M,
|
||
Hunt MA,
|
||
Impellizzeri FM,
|
||
Ishøi L,
|
||
Jones DM,
|
||
King MG,
|
||
Lawrenson PR,
|
||
Leunig M,
|
||
Lewis CL,
|
||
Mathieu N,
|
||
Moksnes H,
|
||
Risberg MA,
|
||
Scholes MJ,
|
||
Semciw AI,
|
||
Serner A,
|
||
Thorborg K,
|
||
Wörner T,
|
||
Dijkstra HP</span><br />
|
||
<span class="medgenPMjournal">Br J Sports Med</span>
|
||
2020 Jun;54(11):631-641.
|
||
Epub 2020 Jan 20
|
||
doi: 10.1136/bjsports-2019-101453.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31959678" target="_blank">31959678</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25842248">Mild to Moderate Hip OA: Joint Preservation or Total Hip Arthroplasty?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Peters CL</span><br />
|
||
<span class="medgenPMjournal">J Arthroplasty</span>
|
||
2015 Jul;30(7):1109-12.
|
||
Epub 2015 Mar 25
|
||
doi: 10.1016/j.arth.2015.02.046.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25842248" target="_blank">25842248</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11730331">Developmental dysplasia of the hip from six months to four years of age.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vitale MG,
|
||
Skaggs DL</span><br />
|
||
<span class="medgenPMjournal">J Am Acad Orthop Surg</span>
|
||
2001 Nov-Dec;9(6):401-11.
|
||
doi: 10.5435/00124635-200111000-00005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11730331" target="_blank">11730331</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7790492">Pelvic remodeling after Salter osteotomy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Saleh JM,
|
||
O'Sullivan ME,
|
||
O'Brien TM</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Orthop</span>
|
||
1995 May-Jun;15(3):342-5.
|
||
doi: 10.1097/01241398-199505000-00016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7790492" target="_blank">7790492</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8370774">Triple innominate osteotomy for acetabular dysplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Faciszewski T,
|
||
Coleman SS,
|
||
Biddulph G</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Orthop</span>
|
||
1993 Jul-Aug;13(4):426-30.
|
||
doi: 10.1097/01241398-199307000-00002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8370774" target="_blank">8370774</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acetabular%20dysplasia%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 (409)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34896582">Residual acetabular dysplasia in congenital hip dysplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">de Courtivron B,
|
||
Brulefert K,
|
||
Portet A,
|
||
Odent T</span><br />
|
||
<span class="medgenPMjournal">Orthop Traumatol Surg Res</span>
|
||
2022 Feb;108(1S):103172.
|
||
Epub 2021 Dec 9
|
||
doi: 10.1016/j.otsr.2021.103172.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34896582" target="_blank">34896582</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32436427">Sclerotic lesions of the femoral head-neck junction for diagnosis of femoroacetabular impingement.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hananouchi T,
|
||
Aoki SK</span><br />
|
||
<span class="medgenPMjournal">J Orthop Surg (Hong Kong)</span>
|
||
2020 Jan-Apr;28(2):2309499020924161.
|
||
doi: 10.1177/2309499020924161.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32436427" target="_blank">32436427</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27379671">The management of residual acetabular dysplasia: updates and controversies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mansour E,
|
||
Eid R,
|
||
Romanos E,
|
||
Ghanem I</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Orthop B</span>
|
||
2017 Jul;26(4):344-349.
|
||
doi: 10.1097/BPB.0000000000000358.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27379671" target="_blank">27379671</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25842248">Mild to Moderate Hip OA: Joint Preservation or Total Hip Arthroplasty?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Peters CL</span><br />
|
||
<span class="medgenPMjournal">J Arthroplasty</span>
|
||
2015 Jul;30(7):1109-12.
|
||
Epub 2015 Mar 25
|
||
doi: 10.1016/j.arth.2015.02.046.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25842248" target="_blank">25842248</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24460107">Incomplete periacetabular acetabuloplasty.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carsi B,
|
||
Al-Hallao S,
|
||
Wahed K,
|
||
Page J,
|
||
Clarke NM</span><br />
|
||
<span class="medgenPMjournal">Acta Orthop</span>
|
||
2014 Feb;85(1):66-70.
|
||
Epub 2014 Jan 24
|
||
doi: 10.3109/17453674.2014.886030.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24460107" target="_blank">24460107</a><a href="/pmc/articles/PMC3940994" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acetabular%20dysplasia%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 (459)</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/37555638">Prevalence and radiological definitions of acetabular dysplasia after the age of 2 years: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">de Vos-Jakobs S,
|
||
Boel F,
|
||
Bramer WM,
|
||
Bierma-Zeinstra SMA,
|
||
Agricola R</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Orthop B</span>
|
||
2024 Jul 1;33(4):334-339.
|
||
Epub 2023 Aug 7
|
||
doi: 10.1097/BPB.0000000000001113.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37555638" target="_blank">37555638</a><a href="/pmc/articles/PMC11132094" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36892224">What is the Rate of Response to Nonoperative Treatment for Hip-Related Pain? A Systematic Review With Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Probst DT,
|
||
Sookochoff MF,
|
||
Harris-Hayes M,
|
||
Prather H,
|
||
Lipsey KL,
|
||
Cheng AL</span><br />
|
||
<span class="medgenPMjournal">J Orthop Sports Phys Ther</span>
|
||
2023 May;53(5):286–306.
|
||
doi: 10.2519/jospt.2023.11666.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36892224" target="_blank">36892224</a><a href="/pmc/articles/PMC10176100" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35470119">Hip survivorship following the Bernese periacetabular osteotomy for the treatment of acetabular dysplasia: A systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tan JHI,
|
||
Tan SHS,
|
||
Rajoo MS,
|
||
Lim AKS,
|
||
Hui JH</span><br />
|
||
<span class="medgenPMjournal">Orthop Traumatol Surg Res</span>
|
||
2022 Jun;108(4):103283.
|
||
Epub 2022 Apr 22
|
||
doi: 10.1016/j.otsr.2022.103283.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35470119" target="_blank">35470119</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31809799">Surgical Outcomes in the Treatment of Concomitant Mild Acetabular Dysplasia and Femoroacetabular Impingement: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tang HC,
|
||
Dienst M</span><br />
|
||
<span class="medgenPMjournal">Arthroscopy</span>
|
||
2020 Apr;36(4):1176-1184.
|
||
Epub 2019 Dec 4
|
||
doi: 10.1016/j.arthro.2019.11.122.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31809799" target="_blank">31809799</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30611355">The Utility of Hip Arthroscopy in the Setting of Acetabular Dysplasia: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adler KL,
|
||
Giordano BD</span><br />
|
||
<span class="medgenPMjournal">Arthroscopy</span>
|
||
2019 Jan;35(1):237-248.
|
||
doi: 10.1016/j.arthro.2018.07.048.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30611355" target="_blank">30611355</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acetabular%20dysplasia%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 (22)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
||
|
||
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|
||
<div class=" bottom">
|
||
|
||
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|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
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||
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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="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=Acetabular%20dysplasia" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
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<div class="portlet mgSection" id="ID_121">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22acetabular%20dysplasia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Acetabular%20dysplasia%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>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Acetabular%20dysplasia" target="_blank">MedlinePlus</a></li></ul></div>
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<a href="/pubmed/clinical?term=Acetabular%20dysplasia" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Acetabular%20dysplasia%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=233069" ref="log$=recordlinks">ClinVar</a>
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<div class="brieflinkpop offscreen_noflow">Related medical variations</div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d20096a68b6b5afccb61ee">Acetabular dysplasia</a>
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<div class="ralinkpop offscreen_noflow">Acetabular dysplasia<div class="brieflinkpopdesc"></div></div>
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<a class="htb" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d20095a68b6b5afccb5d0d">C1328407[conceptid] <span class="number">(1)</span></a>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d20094a68b6b5afccb58f8">"Rheumatology and Immunology Department, Shandong Provincial Hosp... <span class="number">(1)</span></a>
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<div class="ralinkpop offscreen_noflow">"Rheumatology and Immunology Department, Shandong Provincial Hospital Affiliated to Shandong First Medicial University"[submitter] AND "COL2A1"[gene]<div class="brieflinkpopdesc">Search</div></div>
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<div class="tertiary">ClinVar</div>
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