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<meta name="keywords" content="C0265240, cfm1, craniofacial microsomia, craniofacial microsomia 1, craniofacial microsomias, disease or syndrome, dysostosis, otomandibular, dysplasia, facioauriculovertebral, dysplasia, lateral facial, dysplasia, oculoauriculovertebral, dysplasias, facioauriculovertebral, dysplasias, lateral facial, dysplasias, oculoauriculovertebral, expanded spectrum hemifacial microsomia, expanded spectrum of hemifacial microsomia, facial dysplasia, lateral, facial dysplasias, lateral, facio-auriculo-vertebral spectrum, facio-auriculo-vertebral syndrome, facioauriculovertebral dysplasia, facioauriculovertebral dysplasias, facioauriculovertebral sequence, facioauriculovertebral sequences, fav sequence, first and second branchial arch syndrome, first and second pharyngeal arch syndromes, first arch syndrome, first branchial arch syndrome, goldenhar disease, goldenhar gorlin syndrome, goldenhar syndrome, goldenhar-gorlin syndrome, goldenhar-gorlin syndromes, hemifacial microsomia, hfm, lateral facial dysplasia, lateral facial dysplasias, laterofacial microsomia, microsomia, craniofacial, microsomias, craniofacial, moeschler clarren syndrome, oav (oculo-auriculo-vertebral) spectrum, oav (oculoauriculovertebral) dysplasia, oav dysplasia, oav spectrum, oavd, oavs, oculo-auriculo-vertebral dysplasia, oculo-auriculo-vertebral spectrum, oculoauricular vertebral dysplasia, oculoauriculovertebral dysplasia, oculoauriculovertebral dysplasias, oculoauriculovertebral spectrum, oculoauriculovertebral spectrums, oculoauriculovertebral syndrome, oral mandibular auricular syndrome, oral-mandibular-auricular syndrome, oral-mandibular-auricular syndromes, otomandibular dysostosis, otomandibular syndrome, unilateral or bilateral and asymmetric otomandibular dysplasia, 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 rare congenital malformation syndrome, most commonly presenting with hemifacial microsomia associated with ear and/or eye malformations and vertebral anomalies of variable severity. Additional malformations involving the heart, kidneys, central nervous, digestive and skeletal systems may also be associated. The phenotypic spectrum ranges from isolated mild facial asymmetry to severe bilateral craniofacial microsomia and additional multiple extracranial abnormalities. Intelligence is typically normal. The aetiology is poorly understood but is suspected to be heterogeneous and multifactorial. The gene MYT1 (20q13.33) has been implicated in a few rare cases, and chromosomal abnormalities have been associated with some of the congenital malformations associated with this condition. The condition usually occurs sporadically, but autosomal dominant inheritance has been reported." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
|
||
UID=75554
|
||
ConceptID=C0265240
|
||
-->
|
||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Craniofacial microsomia<span class="h1sub">(HFM; OAVS; CFM1)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75554</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.">C0265240</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Facio-auriculo-vertebral Syndrome; First and second branchial arch syndrome; Goldenhar syndrome; Oculo-auriculo-vertebral spectrum</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Otomandibular dysostosis (109393007); Otomandibular syndrome (109393007); Facio-auriculo-vertebral spectrum (367462009); First and second branchial arch syndrome (703973009); Goldenhar syndrome (205418005); Oculoauricular vertebral dysplasia (205418005); Craniofacial microsomia (254026007); Oculo-auriculo-vertebral spectrum (1010685005); Oculoauriculovertebral spectrum (1010685005); OAV (oculo-auriculo-vertebral) spectrum (1010685005)</td></tr>
|
||
<tr><td>Modes of inheritance:</td>
|
||
<td>
|
||
<div class="divPopper rprt" id="moi_988794"><div><strong>Not genetically inherited</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>988794</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier assigned by MedGen (starting with CN) for terms that cannot be identified in NLM's Unified Medical Language system (UMLS) Click for more information.">CN307044</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">clinical entity without genetic inheritance.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/988794">This record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_988794" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Not genetically inherited</a><span> (Orphanet)</span></div></td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help" data-jig="ncbipopper" href="#target-gene-related">Related genes:<img src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div id="target-gene-related" class="display-none">
|
||
Gene(s) associated with related conditions. For conditions<br />
|
||
in a hierarchy, the parent condition will list the genes<br />
|
||
associated with the children conditions.</div></td>
|
||
<td><a target="_blank" href="/gene/344167">FOXI3</a>, <a target="_blank" href="/gene/10992">SF3B2</a></td></tr><tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0015397" target="_blank">MONDO:0015397</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/164210" target="_blank">164210</a>; <a href="https://omim.org/entry/605591" target="_blank">605591</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span> Phenotypic series:</td>
|
||
<td><a href="https://omim.org/phenotypicSeries/PS164210" target="_blank">PS164210</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=141132">ORPHA141132</a></td></tr></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 rare congenital malformation syndrome, most commonly presenting with hemifacial microsomia associated with ear and/or eye malformations and vertebral anomalies of variable severity. Additional malformations involving the heart, kidneys, central nervous, digestive and skeletal systems may also be associated. The phenotypic spectrum ranges from isolated mild facial asymmetry to severe bilateral craniofacial microsomia and additional multiple extracranial abnormalities. Intelligence is typically normal. The aetiology is poorly understood but is suspected to be heterogeneous and multifactorial. The gene MYT1 (20q13.33) has been implicated in a few rare cases, and chromosomal abnormalities have been associated with some of the congenital malformations associated with this condition. The condition usually occurs sporadically, but autosomal dominant inheritance has been reported. [from <a title="US Edition of SNOMED CT" href="http://www.nlm.nih.gov/research/umls/Snomed/us_edition.html" class="defSource" target="_blank">SNOMEDCT_US</a>]</div>
|
||
</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="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=75554" target="_blank" href="/omim/164210">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=75554" ref="ncbi_uid=75554">V</a></span></span><span class="TLline">Craniofacial microsomia</span><ul><li class="TLclosed"><span class="TLline"><a href="/medgen/501171" ref="tree=GTR&ncbi_uid=501171&link_uid=501171" title="View MedGen record for 'Craniofacial microsomia 1'">Craniofacial microsomia 1</a></span></li><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=1830923" target="_blank" href="/omim/612351">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=1830923" ref="ncbi_uid=1830923">V</a></span></span><span class="TLline"><a href="/medgen/1830923" ref="tree=GTR&ncbi_uid=1830923&link_uid=1830923" title="View MedGen record for 'Craniofacial microsomia 2'">Craniofacial microsomia 2</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/1826092" ref="tree=MeSH" title="MedGen record for Branchial arch or oral-acral syndrome">Branchial arch or oral-acral syndrome</a></span><ul><li><span class="matched_ds">Craniofacial microsomia</span><ul><li><span class="TLline"><a href="/medgen/501171" ref="tree=MeSH" title="MedGen record for Craniofacial microsomia 1">Craniofacial microsomia 1</a></span></li><li><span class="TLline"><a href="/medgen/1830923" ref="tree=MeSH" title="MedGen record for Craniofacial microsomia 2">Craniofacial microsomia 2</a></span></li></ul></li></ul></li></ul></div></div></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/37264504">Evaluation of Research Diagnostic Criteria in Craniofacial Microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Renkema RW,
|
||
de Vreugt V,
|
||
Heike CL,
|
||
Padwa BL,
|
||
Forrest CR,
|
||
Dunaway DJ,
|
||
Wolvius EB,
|
||
Caron CJJM,
|
||
Koudstaal MJ</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2023 Sep 1;34(6):1780-1783.
|
||
Epub 2023 Jun 2
|
||
doi: 10.1097/SCS.0000000000009446.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37264504" target="_blank">37264504</a><a href="/pmc/articles/PMC10445631" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34727477">Velopharyngeal Insufficiency in Craniofacial Microsomia: Prevalence, Diagnosis, and Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chan CH,
|
||
Hu AC,
|
||
Jain NS,
|
||
Dang BN,
|
||
Liu MT,
|
||
Bertrand AA,
|
||
Wilson LF,
|
||
Lee JC</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2021 Nov-Dec 01;32(8):2771-2773.
|
||
doi: 10.1097/SCS.0000000000007938.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34727477" target="_blank">34727477</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29264890">The treatment of facial asymmetry: Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kobus K,
|
||
Kobus-Zaleśna K</span><br />
|
||
<span class="medgenPMjournal">Adv Clin Exp Med</span>
|
||
2017 Nov;26(8):1301-1311.
|
||
doi: 10.17219/acem/68976.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29264890" target="_blank">29264890</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22craniofacial%20microsomia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (14)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34730031">Longitudinal Skeletal Growth Analysis of Mandibular Asymmetry in Unoperated Patients With Unilateral Craniofacial Microsomia (UCFM).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shetye PR,
|
||
Grayson BH,
|
||
McCarthy JG</span><br />
|
||
<span class="medgenPMjournal">Cleft Palate Craniofac J</span>
|
||
2023 Jan;60(1):69-74.
|
||
Epub 2021 Nov 3
|
||
doi: 10.1177/10556656211054002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34730031" target="_blank">34730031</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35125269">Hearing impairment and ear anomalies in craniofacial microsomia: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rooijers W,
|
||
Tio PAE,
|
||
van der Schroeff MP,
|
||
Padwa BL,
|
||
Dunaway DJ,
|
||
Forrest CR,
|
||
Koudstaal MJ,
|
||
Caron CJJM</span><br />
|
||
<span class="medgenPMjournal">Int J Oral Maxillofac Surg</span>
|
||
2022 Oct;51(10):1296-1304.
|
||
Epub 2022 Feb 3
|
||
doi: 10.1016/j.ijom.2022.01.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35125269" target="_blank">35125269</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34320587">European Guideline on Craniofacial Microsomia: A Version for Patients and Families.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Renkema RW,
|
||
Spivack OKC;
|
||
ERN CRANIO Working Group on Craniofacial Microsomia</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2022 Jan-Feb 01;33(1):11-14.
|
||
doi: 10.1097/SCS.0000000000007987.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34320587" target="_blank">34320587</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27712817">Craniofacial Microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Brandstetter KA,
|
||
Patel KG</span><br />
|
||
<span class="medgenPMjournal">Facial Plast Surg Clin North Am</span>
|
||
2016 Nov;24(4):495-515.
|
||
doi: 10.1016/j.fsc.2016.06.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27712817" target="_blank">27712817</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25686430">Craniofacial malformations and the orthodontist.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Akram A,
|
||
McKnight MM,
|
||
Bellardie H,
|
||
Beale V,
|
||
Evans RD</span><br />
|
||
<span class="medgenPMjournal">Br Dent J</span>
|
||
2015 Feb 16;218(3):129-41.
|
||
doi: 10.1038/sj.bdj.2015.48.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25686430" target="_blank">25686430</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Craniofacial%20microsomia%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 (133)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37126414">Craniofacial Microsomia: New Updates in Spinal Anomalies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gonçalves Ferraz B,
|
||
Vendramini-Pittoli S,
|
||
Gomes LP,
|
||
Madeira Brandão M,
|
||
Alonso N,
|
||
Tonello C</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2023 Jun 1;34(4):e398-e401.
|
||
Epub 2023 May 1
|
||
doi: 10.1097/SCS.0000000000009326.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37126414" target="_blank">37126414</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35125269">Hearing impairment and ear anomalies in craniofacial microsomia: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rooijers W,
|
||
Tio PAE,
|
||
van der Schroeff MP,
|
||
Padwa BL,
|
||
Dunaway DJ,
|
||
Forrest CR,
|
||
Koudstaal MJ,
|
||
Caron CJJM</span><br />
|
||
<span class="medgenPMjournal">Int J Oral Maxillofac Surg</span>
|
||
2022 Oct;51(10):1296-1304.
|
||
Epub 2022 Feb 3
|
||
doi: 10.1016/j.ijom.2022.01.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35125269" target="_blank">35125269</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33215817">Genomic imbalances in craniofacial microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Spineli-Silva S,
|
||
Sgardioli IC,
|
||
Dos Santos AP,
|
||
Bergamini LL,
|
||
Monlleó IL,
|
||
Fontes MIB,
|
||
Félix TM,
|
||
Ribeiro EM,
|
||
Xavier AC,
|
||
Lustosa-Mendes E,
|
||
Gil-da-Silva-Lopes VL,
|
||
Vieira TP</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet C Semin Med Genet</span>
|
||
2020 Dec;184(4):970-985.
|
||
Epub 2020 Nov 20
|
||
doi: 10.1002/ajmg.c.31857.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33215817" target="_blank">33215817</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30851752">Craniofacial Microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Birgfeld C,
|
||
Heike C</span><br />
|
||
<span class="medgenPMjournal">Clin Plast Surg</span>
|
||
2019 Apr;46(2):207-221.
|
||
doi: 10.1016/j.cps.2018.12.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30851752" target="_blank">30851752</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27712817">Craniofacial Microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Brandstetter KA,
|
||
Patel KG</span><br />
|
||
<span class="medgenPMjournal">Facial Plast Surg Clin North Am</span>
|
||
2016 Nov;24(4):495-515.
|
||
doi: 10.1016/j.fsc.2016.06.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27712817" target="_blank">27712817</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Craniofacial%20microsomia%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 (89)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37852887">Condylar resorption post mandibular distraction osteogenesis in craniofacial microsomia: A retrospective study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shu KY,
|
||
Liu W,
|
||
Zhao JL,
|
||
Zhang ZY,
|
||
Shan BG,
|
||
Li XY,
|
||
Ma LK</span><br />
|
||
<span class="medgenPMjournal">J Craniomaxillofac Surg</span>
|
||
2023 Nov;51(11):675-681.
|
||
Epub 2023 Oct 6
|
||
doi: 10.1016/j.jcms.2023.10.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37852887" target="_blank">37852887</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29084117">A Review of Randomized Controlled Trials in Cleft and Craniofacial Surgery.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bekisz JM,
|
||
Fryml E,
|
||
Flores RL</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2018 Mar;29(2):293-301.
|
||
doi: 10.1097/SCS.0000000000004100.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29084117" target="_blank">29084117</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27891784">Characterizing facial features in individuals with craniofacial microsomia: A systematic approach for clinical research.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Heike CL,
|
||
Wallace E,
|
||
Speltz ML,
|
||
Siebold B,
|
||
Werler MM,
|
||
Hing AV,
|
||
Birgfeld CB,
|
||
Collett BR,
|
||
Leroux BG,
|
||
Luquetti DV</span><br />
|
||
<span class="medgenPMjournal">Birth Defects Res A Clin Mol Teratol</span>
|
||
2016 Nov;106(11):915-926.
|
||
doi: 10.1002/bdra.23560.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27891784" target="_blank">27891784</a><a href="/pmc/articles/PMC11749019" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27763969">Orbital Expansion for Congenital Anophthalmia May Be Achievable in Infancy But Not in Childhood.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Morrow BT,
|
||
Albright WB,
|
||
Neves RI,
|
||
Wilkinson MJ,
|
||
Samson TD</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2016 Oct;27(7):1642-1646.
|
||
doi: 10.1097/SCS.0000000000002937.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27763969" target="_blank">27763969</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17993874">Effect of calcium sulfate pellets on early bone mineralization in distraction osteogenesis for craniofacial microsomia in adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kim JY,
|
||
Cho BC</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2007 Nov;18(6):1309-21.
|
||
doi: 10.1097/SCS.0b013e3180a771c6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17993874" target="_blank">17993874</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Craniofacial%20microsomia%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 (10)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36608091">Spontaneous Closure of Congenital Cranial Defect: Is Early Surgical Intervention Warranted?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Seu MY,
|
||
Aminzada A,
|
||
Harmon KA,
|
||
Guidetti M,
|
||
Espinoza Orías AA,
|
||
Figueroa AA,
|
||
Tragos C</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2023 Jan-Feb 01;34(1):e96-e98.
|
||
Epub 2022 Nov 15
|
||
doi: 10.1097/SCS.0000000000009117.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36608091" target="_blank">36608091</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34261967">Determination of Extra Craniofacial Abnormalities in Patients With Craniofacial Microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raposo BK,
|
||
Ferreira GB,
|
||
Silva ABDE,
|
||
Ono MCC,
|
||
de Souza J,
|
||
da Silva Freitas R</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2022 Jan-Feb 01;33(1):230-232.
|
||
doi: 10.1097/SCS.0000000000007962.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34261967" target="_blank">34261967</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33900643">Craniofacial microsomia: Reflections on diagnosis and severity assessment based on a series of cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bergamini LL,
|
||
Spineli-Silva S,
|
||
Félix TM,
|
||
Gil-da-Silva-Lopes VL,
|
||
Vieira TP,
|
||
Ribeiro EM,
|
||
Xavier AC,
|
||
Lustosa-Mendes E,
|
||
Fontes MÍB,
|
||
Monlleó IL</span><br />
|
||
<span class="medgenPMjournal">Congenit Anom (Kyoto)</span>
|
||
2021 Sep;61(5):148-158.
|
||
Epub 2021 May 10
|
||
doi: 10.1111/cga.12422.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33900643" target="_blank">33900643</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7813161">The role of distraction osteogenesis in the reconstruction of the mandible in unilateral craniofacial microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McCarthy JG</span><br />
|
||
<span class="medgenPMjournal">Clin Plast Surg</span>
|
||
1994 Oct;21(4):625-31.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7813161" target="_blank">7813161</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2467470">Reconstruction of craniofacial microsomia and hemifacial atrophy with free latissimus dorsi flap.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pisarek W</span><br />
|
||
<span class="medgenPMjournal">Acta Chir Plast</span>
|
||
1988;30(4):194-201.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2467470" target="_blank">2467470</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Craniofacial%20microsomia%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 (42)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37126414">Craniofacial Microsomia: New Updates in Spinal Anomalies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gonçalves Ferraz B,
|
||
Vendramini-Pittoli S,
|
||
Gomes LP,
|
||
Madeira Brandão M,
|
||
Alonso N,
|
||
Tonello C</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2023 Jun 1;34(4):e398-e401.
|
||
Epub 2023 May 1
|
||
doi: 10.1097/SCS.0000000000009326.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37126414" target="_blank">37126414</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36608091">Spontaneous Closure of Congenital Cranial Defect: Is Early Surgical Intervention Warranted?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Seu MY,
|
||
Aminzada A,
|
||
Harmon KA,
|
||
Guidetti M,
|
||
Espinoza Orías AA,
|
||
Figueroa AA,
|
||
Tragos C</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2023 Jan-Feb 01;34(1):e96-e98.
|
||
Epub 2022 Nov 15
|
||
doi: 10.1097/SCS.0000000000009117.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36608091" target="_blank">36608091</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34261967">Determination of Extra Craniofacial Abnormalities in Patients With Craniofacial Microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Raposo BK,
|
||
Ferreira GB,
|
||
Silva ABDE,
|
||
Ono MCC,
|
||
de Souza J,
|
||
da Silva Freitas R</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2022 Jan-Feb 01;33(1):230-232.
|
||
doi: 10.1097/SCS.0000000000007962.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34261967" target="_blank">34261967</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33752938">Ocular and adnexal anomalies in craniofacial microsomia: Type and prevalence in a multicentre cohort study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rooijers W,
|
||
Renkema RW,
|
||
Loudon SE,
|
||
Khoshnaw T,
|
||
Padwa BL,
|
||
Dunaway DJ,
|
||
Koudstaal MJ,
|
||
Forrest CR,
|
||
Caron CJJM</span><br />
|
||
<span class="medgenPMjournal">Int J Oral Maxillofac Surg</span>
|
||
2021 Oct;50(10):1303-1311.
|
||
Epub 2021 Mar 20
|
||
doi: 10.1016/j.ijom.2021.02.032.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33752938" target="_blank">33752938</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29685618">Neurodevelopment of Infants with and without Craniofacial Microsomia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Speltz ML,
|
||
Kapp-Simon KA,
|
||
Johns AL,
|
||
Wallace ER,
|
||
Collett BR,
|
||
Magee L,
|
||
Leroux BG,
|
||
Luquetti DV,
|
||
Heike CL</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2018 Jul;198:226-233.e3.
|
||
Epub 2018 Apr 22
|
||
doi: 10.1016/j.jpeds.2018.02.076.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29685618" target="_blank">29685618</a><a href="/pmc/articles/PMC6019149" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Craniofacial%20microsomia%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 (54)</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/35125269">Hearing impairment and ear anomalies in craniofacial microsomia: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rooijers W,
|
||
Tio PAE,
|
||
van der Schroeff MP,
|
||
Padwa BL,
|
||
Dunaway DJ,
|
||
Forrest CR,
|
||
Koudstaal MJ,
|
||
Caron CJJM</span><br />
|
||
<span class="medgenPMjournal">Int J Oral Maxillofac Surg</span>
|
||
2022 Oct;51(10):1296-1304.
|
||
Epub 2022 Feb 3
|
||
doi: 10.1016/j.ijom.2022.01.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35125269" target="_blank">35125269</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32217034">Ocular and adnexal anomalies in craniofacial microsomia: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rooijers W,
|
||
Caron CJJM,
|
||
Loudon SE,
|
||
Padwa BL,
|
||
Dunaway DJ,
|
||
Forrest CR,
|
||
Koudstaal MJ</span><br />
|
||
<span class="medgenPMjournal">Int J Oral Maxillofac Surg</span>
|
||
2020 Sep;49(9):1107-1114.
|
||
Epub 2020 Mar 23
|
||
doi: 10.1016/j.ijom.2020.03.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32217034" target="_blank">32217034</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31608577">Dental anomalies in craniofacial microsomia: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Elsten EECM,
|
||
Caron CJJM,
|
||
Dunaway DJ,
|
||
Padwa BL,
|
||
Forrest C,
|
||
Koudstaal MJ</span><br />
|
||
<span class="medgenPMjournal">Orthod Craniofac Res</span>
|
||
2020 Feb;23(1):16-26.
|
||
Epub 2019 Oct 28
|
||
doi: 10.1111/ocr.12351.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31608577" target="_blank">31608577</a><a href="/pmc/articles/PMC7003932" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28669484">Vertebral anomalies in craniofacial microsomia: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Renkema RW,
|
||
Caron CJJM,
|
||
Mathijssen IMJ,
|
||
Wolvius EB,
|
||
Dunaway DJ,
|
||
Forrest CR,
|
||
Padwa BL,
|
||
Koudstaal MJ</span><br />
|
||
<span class="medgenPMjournal">Int J Oral Maxillofac Surg</span>
|
||
2017 Oct;46(10):1319-1329.
|
||
Epub 2017 Jun 29
|
||
doi: 10.1016/j.ijom.2017.04.025.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28669484" target="_blank">28669484</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25771070">Feeding difficulties in craniofacial microsomia: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Caron CJ,
|
||
Pluijmers BI,
|
||
Joosten KF,
|
||
Mathijssen IM,
|
||
van der Schroeff MP,
|
||
Dunaway DJ,
|
||
Wolvius EB,
|
||
Koudstaal MJ</span><br />
|
||
<span class="medgenPMjournal">Int J Oral Maxillofac Surg</span>
|
||
2015 Jun;44(6):732-7.
|
||
Epub 2015 Mar 12
|
||
doi: 10.1016/j.ijom.2015.02.014.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25771070" target="_blank">25771070</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Craniofacial%20microsomia%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 (14)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
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|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="https://www.omim.org/phenotypicSeries/PS164210" target="_blank">OMIM</a></li><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=141132" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Craniofacial%20microsomia" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22craniofacial%20microsomia%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(%22Craniofacial%20microsomia%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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<a href="https://www.nlm.nih.gov/careers/careers.html" class="text-white">Careers</a></p>
|
||
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<div class="row">
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<div class="col-lg-12 centered-lg">
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<nav class="bottom-links">
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<li>
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||
<a class="text-white" href="//www.nlm.nih.gov/">NLM</a>
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||
</li>
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<li>
|
||
<a class="text-white" href="https://www.nih.gov/">NIH</a>
|
||
</li>
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||
<li>
|
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<a class="text-white" href="https://www.hhs.gov/">HHS</a>
|
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</li>
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<li>
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<a class="text-white" href="https://www.usa.gov/">USA.gov</a>
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