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<!--
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UID=140861
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ConceptID=C0424690
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Skull asymmetry</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>140861</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.">C0424690</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Asymmetric skull; Asymmetry of skull</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Asymmetrical skull (248372000)</td></tr>
|
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<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0002678">HP:0002678</a></td></tr>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Skull asymmetry</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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="TLline"><a href="/medgen/892434" ref="tree=MeSH" title="MedGen record for Abnormal axial skeleton morphology">Abnormal axial skeleton morphology</a></span><ul><li><span class="TLline"><a href="/medgen/488801" ref="tree=MeSH" title="MedGen record for Abnormal skull morphology">Abnormal skull morphology</a></span><ul><li><span class="TLline"><a href="/medgen/871212" ref="tree=MeSH" title="MedGen record for Abnormal calvaria morphology">Abnormal calvaria morphology</a></span><ul><li><span class="matched_ds">Skull asymmetry</span></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>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_6009"><div><strong>Langer-Giedion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>6009</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0023003</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Trichorhinophalangeal syndrome (TRPS) comprises TRPS I (caused by a heterozygous pathogenic variant in TRPS1) and TRPS II (caused by a contiguous gene deletion of TRPS1, RAD21, and EXT1). Both TRPS types are characterized by distinctive facial features (large nose with broad nasal ridge and tip and underdeveloped alae; thick and broad medial eyebrows; long philtrum; thin vermilion of the upper lip; and large prominent ears); ectodermal features (fine, sparse, depigmented, and slow-growing hair and dystrophic nails); and skeletal findings (short stature, brachydactyly with ulnar or radial deviation of the fingers, short feet, and early, marked hip dysplasia). TRPS II is additionally characterized by multiple osteochondromas and an increased risk of mild-to-moderate intellectual disability.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/6009">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_64221"><div><strong>Saethre-Chotzen syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>64221</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.">C0175699</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Classic Saethre-Chotzen syndrome (SCS) is characterized by coronal synostosis (unilateral or bilateral), facial asymmetry (particularly in individuals with unicoronal synostosis), strabismus, ptosis, and characteristic appearance of the ear (small pinna with a prominent superior and/or inferior crus). Syndactyly of digits two and three of the hand is variably present. Cognitive development is usually normal, although those with a large genomic deletion are at an increased risk for intellectual challenges. Less common manifestations of SCS include other skeletal findings (parietal foramina, vertebral segmentation defects, radioulnar synostosis, maxillary hypoplasia, ocular hypertelorism, hallux valgus, duplicated or curved distal hallux), hypertelorism, palatal anomalies, obstructive sleep apnea, increased intracranial pressure, short stature, and congenital heart malformations.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/64221">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_163201"><div><strong>Gomez Lopez Hernandez syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>163201</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.">C0795959</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Gomez-Lopez-Hernandez syndrome (GLHS), also known as cerebellotrigeminal dermal dysplasia, is a rare neurocutaneous syndrome classically characterized by the triad of rhombencephalosynapsis, trigeminal anesthesia, often giving rise to corneal opacities, and bilateral parietal or parietooccipital alopecia. However, trigeminal anesthesia is an inconsistent finding (summary by Sukhudyan et al., 2010).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/163201">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_167100"><div><strong>3MC syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>167100</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.">C0796059</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The term '3MC syndrome' encompasses 4 rare autosomal recessive disorders that were previously designated the Carnevale, Mingarelli, Malpuech, and Michels syndromes, respectively. The main features of these syndromes are facial dysmorphism that includes hypertelorism, blepharophimosis, blepharoptosis, and highly arched eyebrows, which are present in 70 to 95% of cases. Cleft lip and palate, postnatal growth deficiency, cognitive impairment, and hearing loss are also consistent findings, occurring in 40 to 68% of cases. Craniosynostosis, radioulnar synostosis, and genital and vesicorenal anomalies occur in 20 to 30% of cases. Rare features include anterior chamber defects, cardiac anomalies, caudal appendage, umbilical hernia (omphalocele), and diastasis recti (summary by Rooryck et al., 2011). Genetic Heterogeneity of 3MC Syndrome Also see 3MC syndrome-2 (3MC2; 265050), caused by mutation in the COLEC11 gene (612502), and 3MC syndrome-3 (3MC3; 248340), caused by mutation in the COLEC1 gene (607620).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/167100">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_167115"><div><strong>3MC syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>167115</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.">C0796279</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The term '3MC syndrome' encompasses 4 rare autosomal recessive disorders that were previously designated the Carnevale, Mingarelli, Malpuech, and Michels syndromes, respectively. The main features of these syndromes are facial dysmorphism that includes hypertelorism, blepharophimosis, blepharoptosis, and highly arched eyebrows, which are present in 70 to 95% of cases. Cleft lip and palate, postnatal growth deficiency, cognitive impairment, and hearing loss are also consistent findings, occurring in 40 to 68% of cases. Craniosynostosis, radioulnar synostosis, and genital and vesicorenal anomalies occur in 20 to 30% of cases. Rare features include anterior chamber defects, cardiac anomalies, caudal appendage, umbilical hernia (omphalocele), and diastasis recti (summary by Rooryck et al., 2011). For a discussion of genetic heterogeneity of 3MC syndrome, see 3MC1 (257920).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/167115">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_414158"><div><strong>Lethal polymalformative syndrome, Boissel type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>414158</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.">C2752001</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Growth retardation, developmental delay, and facial dysmorphism (GDFD) is an autosomal recessive multiple congenital anomaly syndrome characterized by severe psychomotor retardation, poor overall growth, and dysmorphic facial features. Additional features may include cardiac malformations and deafness (summary by Daoud et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/414158">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766431"><div><strong>Cornelia de Lange syndrome 4</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766431</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.">C3553517</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cornelia de Lange syndrome (CdLS) encompasses a spectrum of findings from mild to severe. Severe (classic) CdLS is characterized by distinctive facial features, growth restriction (prenatal onset; <5th centile throughout life), hypertrichosis, and upper-limb reduction defects that range from subtle phalangeal abnormalities to oligodactyly (missing digits). Craniofacial features include synophrys, highly arched and/or thick eyebrows, long eyelashes, short nasal bridge with anteverted nares, small widely spaced teeth, and microcephaly. Individuals with a milder phenotype have less severe growth, cognitive, and limb involvement, but often have facial features consistent with CdLS. Across the CdLS spectrum IQ ranges from below 30 to 102 (mean: 53). Many individuals demonstrate autistic and self-destructive tendencies. Other frequent findings include cardiac septal defects, gastrointestinal dysfunction, hearing loss, myopia, and cryptorchidism or hypoplastic genitalia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766431">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1800305"><div><strong>Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1800305</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.">C5568882</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of global developmental delay and intellectual disability, progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals and dysmorphic craniofacial features (including microcephaly, hypertelorism, epicanthal folds, mild ptosis, strabismus, malar hypoplasia, short nose, depressed nasal bridge, full lips, small, low-set ears and short neck). Craniosynostosis, generalized hypotonia, as well as asymmetry of the cerebral hemispheres and mild thinning of the corpus callosum on brain imaging have also been described.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1800305">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_167100" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">3MC syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_167115" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">3MC syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766431" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cornelia de Lange syndrome 4</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_163201" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Gomez Lopez Hernandez syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_6009" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Langer-Giedion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_414158" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lethal polymalformative syndrome, Boissel type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1800305" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_64221" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Saethre-Chotzen syndrome</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31232996">Treatment of Deformational Plagiocephaly With Physiotherapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Di Chiara A,
|
||
La Rosa E,
|
||
Ramieri V,
|
||
Vellone V,
|
||
Cascone P</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2019 Oct;30(7):2008-2013.
|
||
doi: 10.1097/SCS.0000000000005665.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31232996" target="_blank">31232996</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22920774">Evidence-based care of the child with deformational plagiocephaly, part II: management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Flannery AB,
|
||
Looman WS,
|
||
Kemper K</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Health Care</span>
|
||
2012 Sep-Oct;26(5):320-31.
|
||
doi: 10.1016/j.pedhc.2011.10.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22920774" target="_blank">22920774</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18678803">Nonsurgical treatment of deformational plagiocephaly: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xia JJ,
|
||
Kennedy KA,
|
||
Teichgraeber JF,
|
||
Wu KQ,
|
||
Baumgartner JB,
|
||
Gateno J</span><br />
|
||
<span class="medgenPMjournal">Arch Pediatr Adolesc Med</span>
|
||
2008 Aug;162(8):719-27.
|
||
doi: 10.1001/archpedi.162.8.719.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18678803" target="_blank">18678803</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22skull%20asymmetry%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 (4)</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/37382098">Ophthalmic Manifestations of Unilateral Coronal Synostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Huynh EM,
|
||
Elhusseiny AM,
|
||
Dagi LR</span><br />
|
||
<span class="medgenPMjournal">Curr Eye Res</span>
|
||
2023 Oct;48(10):879-886.
|
||
Epub 2023 Jun 29
|
||
doi: 10.1080/02713683.2023.2224536.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37382098" target="_blank">37382098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28746283">Head Orthosis Therapy in Positional Plagiocephaly: Influence of Age and Severity of Asymmetry on Effect and Duration of Therapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kunz F,
|
||
Schweitzer T,
|
||
Kunz J,
|
||
Waßmuth N,
|
||
Stellzig-Eisenhauer A,
|
||
Böhm H,
|
||
Meyer-Marcotty P,
|
||
Linz C</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2017 Aug;140(2):349-358.
|
||
doi: 10.1097/PRS.0000000000003517.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28746283" target="_blank">28746283</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20066632">Spontaneous resolution of calcified cephalhematomas of infancy: report of two cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Daglioglu E,
|
||
Okay O,
|
||
Hatipoglu HG,
|
||
Dalgic A,
|
||
Ergungor F</span><br />
|
||
<span class="medgenPMjournal">Turk Neurosurg</span>
|
||
2010 Jan;20(1):96-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20066632" target="_blank">20066632</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18678803">Nonsurgical treatment of deformational plagiocephaly: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xia JJ,
|
||
Kennedy KA,
|
||
Teichgraeber JF,
|
||
Wu KQ,
|
||
Baumgartner JB,
|
||
Gateno J</span><br />
|
||
<span class="medgenPMjournal">Arch Pediatr Adolesc Med</span>
|
||
2008 Aug;162(8):719-27.
|
||
doi: 10.1001/archpedi.162.8.719.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18678803" target="_blank">18678803</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3696912">Skull asymmetry and handedness in adults: a possibility of their association with lateral head turning in infancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Myslobodsky MS,
|
||
Ingraham LJ,
|
||
Weinberger DR</span><br />
|
||
<span class="medgenPMjournal">Percept Mot Skills</span>
|
||
1987 Oct;65(2):415-21.
|
||
doi: 10.2466/pms.1987.65.2.415.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3696912" target="_blank">3696912</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Skull%20asymmetry%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 (15)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37382098">Ophthalmic Manifestations of Unilateral Coronal Synostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Huynh EM,
|
||
Elhusseiny AM,
|
||
Dagi LR</span><br />
|
||
<span class="medgenPMjournal">Curr Eye Res</span>
|
||
2023 Oct;48(10):879-886.
|
||
Epub 2023 Jun 29
|
||
doi: 10.1080/02713683.2023.2224536.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37382098" target="_blank">37382098</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31232996">Treatment of Deformational Plagiocephaly With Physiotherapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Di Chiara A,
|
||
La Rosa E,
|
||
Ramieri V,
|
||
Vellone V,
|
||
Cascone P</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2019 Oct;30(7):2008-2013.
|
||
doi: 10.1097/SCS.0000000000005665.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31232996" target="_blank">31232996</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23816888">Skull asymmetry as an unusual presentation of an intracranial tumour.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Boyle M,
|
||
Hurley A,
|
||
Curtis E</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neurosurg</span>
|
||
2012;48(5):333-4.
|
||
Epub 2013 Jun 25
|
||
doi: 10.1159/000351548.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23816888" target="_blank">23816888</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22532473">Unilateral and bilateral expression of a quantitative trait: asymmetry and symmetry in coronal craniosynostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Heuzé Y,
|
||
Martínez-Abadías N,
|
||
Stella JM,
|
||
Senders CW,
|
||
Boyadjiev SA,
|
||
Lo LJ,
|
||
Richtsmeier JT</span><br />
|
||
<span class="medgenPMjournal">J Exp Zool B Mol Dev Evol</span>
|
||
2012 Mar;318(2):109-22.
|
||
doi: 10.1002/jezb.21449.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22532473" target="_blank">22532473</a><a href="/pmc/articles/PMC3315613" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20066632">Spontaneous resolution of calcified cephalhematomas of infancy: report of two cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Daglioglu E,
|
||
Okay O,
|
||
Hatipoglu HG,
|
||
Dalgic A,
|
||
Ergungor F</span><br />
|
||
<span class="medgenPMjournal">Turk Neurosurg</span>
|
||
2010 Jan;20(1):96-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20066632" target="_blank">20066632</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Skull%20asymmetry%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 (17)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/18678803">Nonsurgical treatment of deformational plagiocephaly: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xia JJ,
|
||
Kennedy KA,
|
||
Teichgraeber JF,
|
||
Wu KQ,
|
||
Baumgartner JB,
|
||
Gateno J</span><br />
|
||
<span class="medgenPMjournal">Arch Pediatr Adolesc Med</span>
|
||
2008 Aug;162(8):719-27.
|
||
doi: 10.1001/archpedi.162.8.719.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18678803" target="_blank">18678803</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Skull%20asymmetry%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 (1)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30155873">Incidence, number and topography of Wormian bones in Greek adult dry skulls.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Natsis K,
|
||
Piagkou M,
|
||
Lazaridis N,
|
||
Anastasopoulos N,
|
||
Nousios G,
|
||
Piagkos G,
|
||
Loukas M</span><br />
|
||
<span class="medgenPMjournal">Folia Morphol (Warsz)</span>
|
||
2019;78(2):359-370.
|
||
Epub 2018 Aug 29
|
||
doi: 10.5603/FM.a2018.0078.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30155873" target="_blank">30155873</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22418716">Squamosal suture synostosis: a cause of atypical skull asymmetry.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Smartt JM Jr,
|
||
Singh DJ,
|
||
Reid RR,
|
||
Hellinger JC,
|
||
Hsu VM,
|
||
Bartlett SP</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2012 Jul;130(1):165-176.
|
||
doi: 10.1097/PRS.0b013e318254b271.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22418716" target="_blank">22418716</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20066632">Spontaneous resolution of calcified cephalhematomas of infancy: report of two cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Daglioglu E,
|
||
Okay O,
|
||
Hatipoglu HG,
|
||
Dalgic A,
|
||
Ergungor F</span><br />
|
||
<span class="medgenPMjournal">Turk Neurosurg</span>
|
||
2010 Jan;20(1):96-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20066632" target="_blank">20066632</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18678803">Nonsurgical treatment of deformational plagiocephaly: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xia JJ,
|
||
Kennedy KA,
|
||
Teichgraeber JF,
|
||
Wu KQ,
|
||
Baumgartner JB,
|
||
Gateno J</span><br />
|
||
<span class="medgenPMjournal">Arch Pediatr Adolesc Med</span>
|
||
2008 Aug;162(8):719-27.
|
||
doi: 10.1001/archpedi.162.8.719.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18678803" target="_blank">18678803</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3696912">Skull asymmetry and handedness in adults: a possibility of their association with lateral head turning in infancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Myslobodsky MS,
|
||
Ingraham LJ,
|
||
Weinberger DR</span><br />
|
||
<span class="medgenPMjournal">Percept Mot Skills</span>
|
||
1987 Oct;65(2):415-21.
|
||
doi: 10.2466/pms.1987.65.2.415.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3696912" target="_blank">3696912</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Skull%20asymmetry%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 (9)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36847664">Neurocognitive Outcomes in Deformational Plagiocephaly: Is There an Association between Morphologic Severity and Results?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Park KE,
|
||
Chandler L,
|
||
Ahmad M,
|
||
Singh A,
|
||
Allam O,
|
||
Mets E,
|
||
Bridgett DJ,
|
||
Persing JA,
|
||
Alperovich M</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2023 Sep 1;152(3):488e-498e.
|
||
Epub 2023 Feb 28
|
||
doi: 10.1097/PRS.0000000000010330.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36847664" target="_blank">36847664</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30920633">Correlation between otitis media with effusion and cranial deformation in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Orlando MP,
|
||
Bonanno MA,
|
||
Russo FY,
|
||
Ralli M,
|
||
Turchetta R,
|
||
Passali FM,
|
||
Minni A,
|
||
Greco A,
|
||
De Vincentiis M,
|
||
Tattoli M</span><br />
|
||
<span class="medgenPMjournal">Eur Rev Med Pharmacol Sci</span>
|
||
2019 Mar;23(1 Suppl):55-59.
|
||
doi: 10.26355/eurrev_201903_17350.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30920633" target="_blank">30920633</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23274633">Ping pong fractures: treatment using a new medical device.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">López-Elizalde R,
|
||
Leyva-Mastrapa T,
|
||
Muñoz-Serrano JA,
|
||
Godínez-Rubí M,
|
||
Preciado-Barón K,
|
||
Velázquez-Santana H,
|
||
Santana-Ramírez A</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2013 Apr;29(4):679-83.
|
||
Epub 2012 Dec 30
|
||
doi: 10.1007/s00381-012-1979-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23274633" target="_blank">23274633</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22191437">The inter-rater and intra-rater reliability of a modified "severity scale for assessment of plagiocephaly" among physical therapists.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Öhman A</span><br />
|
||
<span class="medgenPMjournal">Physiother Theory Pract</span>
|
||
2012 Jul;28(5):402-6.
|
||
Epub 2011 Dec 22
|
||
doi: 10.3109/09593985.2011.639850.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22191437" target="_blank">22191437</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3696912">Skull asymmetry and handedness in adults: a possibility of their association with lateral head turning in infancy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Myslobodsky MS,
|
||
Ingraham LJ,
|
||
Weinberger DR</span><br />
|
||
<span class="medgenPMjournal">Percept Mot Skills</span>
|
||
1987 Oct;65(2):415-21.
|
||
doi: 10.2466/pms.1987.65.2.415.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3696912" target="_blank">3696912</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Skull%20asymmetry%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (7)</a></div></div>
|
||
</div>
|
||
|
||
<div 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/18678803">Nonsurgical treatment of deformational plagiocephaly: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xia JJ,
|
||
Kennedy KA,
|
||
Teichgraeber JF,
|
||
Wu KQ,
|
||
Baumgartner JB,
|
||
Gateno J</span><br />
|
||
<span class="medgenPMjournal">Arch Pediatr Adolesc Med</span>
|
||
2008 Aug;162(8):719-27.
|
||
doi: 10.1001/archpedi.162.8.719.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18678803" target="_blank">18678803</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Skull%20asymmetry%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 (1)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
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|
||
|
||
</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">
|
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<div class="portlet mgSection" id="ID_113">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul id="my-toc"></ul></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>
|
||
<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Skull%20asymmetry" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
||
<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=(%22skull%20asymmetry%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
|
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|
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|
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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=Skull%20asymmetry" target="_blank">MedlinePlus</a></li></ul></div>
|
||
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|
||
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|
||
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|
||
<div class="portlet_head">
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||
<li>
|
||
<a href="/pubmed/clinical?term=Skull%20asymmetry" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed?term=Skull%20asymmetry%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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|
||
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|
||
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|
||
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|
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|
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<!-- MedGen supplemental column ends here -->
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<h3>Related information</h3>
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=140861" ref="log$=recordlinks">PMC Articles</a>
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<div class="brieflinkpop offscreen_noflow">Related information in PubMed Central Links</div>
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=140861" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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|
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Clear
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Turn On
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<ul id="activity">
|
||
<li class="ra_rcd ralinkpopper two_line">
|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d5512284f3725e591e1b62">Skull asymmetry</a>
|
||
<div class="ralinkpop offscreen_noflow">Skull asymmetry<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary">MedGen</div>
|
||
</li>
|
||
<li class="ra_rcd ralinkpopper two_line">
|
||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d55120cde49f3df7c55d5d">Partial duplication of the distal phalanx of the 2nd finger</a>
|
||
<div class="ralinkpop offscreen_noflow">Partial duplication of the distal phalanx of the 2nd finger<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary">MedGen</div>
|
||
</li>
|
||
<li class="ra_rcd ralinkpopper two_line">
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d5511e67c23b31e099721d">Partial duplication of the distal phalanx of the 3rd finger</a>
|
||
<div class="ralinkpop offscreen_noflow">Partial duplication of the distal phalanx of the 3rd finger<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary">MedGen</div>
|
||
</li>
|
||
<li class="ra_rcd ralinkpopper two_line">
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=4" href="/portal/utils/pageresolver.fcgi?recordid=67d5511ccde49f3df7c54ee2">Absent first metatarsal</a>
|
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<div class="ralinkpop offscreen_noflow">Absent first metatarsal<div class="brieflinkpopdesc"></div></div>
|
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<div class="tertiary">MedGen</div>
|
||
</li>
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<li class="ra_rcd ralinkpopper two_line">
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=5" href="/portal/utils/pageresolver.fcgi?recordid=67d5510b67c23b31e09921f5">Saethre-Chotzen Syndrome - GeneReviews®</a>
|
||
<div class="ralinkpop offscreen_noflow">Saethre-Chotzen Syndrome - GeneReviews®<div class="brieflinkpopdesc"></div></div>
|
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