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<!--
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UID=866810
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ConceptID=C4021164
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Bicoronal synostosis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>866810</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.">C4021164</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Bilateral coronal craniosynostosis; Bilateral coronal suture craniosynostosis; Bilateral coronal suture synostosis</td></tr>
|
||
<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:0011318">HP:0011318</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln">Synostosis affecting the right and the left coronal suture. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</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>
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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="TLline">Bicoronal synostosis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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/871380" ref="tree=MeSH" title="MedGen record for Abnormal cranial suture/fontanelle morphology">Abnormal cranial suture/fontanelle morphology</a></span><ul><li><span class="TLline"><a href="/medgen/868996" ref="tree=MeSH" title="MedGen record for Abnormality of cranial sutures">Abnormality of cranial sutures</a></span><ul><li><span class="TLline"><a href="/medgen/1163" ref="tree=MeSH" title="MedGen record for Craniosynostosis syndrome">Craniosynostosis syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/344694" ref="tree=MeSH" title="MedGen record for Coronal craniosynostosis">Coronal craniosynostosis</a></span><ul><li><span class="matched_ds">Bicoronal synostosis</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<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_120532"><div><strong>Baller-Gerold syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>120532</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.">C0265308</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Baller-Gerold syndrome (BGS) can be suspected at birth in an infant with craniosynostosis and upper limb abnormality. The coronal suture is most commonly affected; the metopic, lambdoid, and sagittal sutures may also be involved alone or in combination. Upper limb abnormality can include a combination of thumb hypo- or aplasia and radial hypo- or aplasia and may be asymmetric. Malformation or absence of carpal or metacarpal bones has also been described. Skin lesions may appear anytime within the first few years after birth, typically beginning with erythema of the face and extremities and evolving into poikiloderma. Slow growth is apparent in infancy with eventual height and length typically at 4 SD below the mean.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/120532">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_167083"><div><strong>Curry-Jones syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>167083</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.">C0795915</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Curry-Jones syndrome (CRJS) is a multisystem disorder characterized by patchy skin lesions, polysyndactyly, diverse cerebral malformations, unicoronal craniosynostosis, iris colobomas, microphthalmia, and intestinal malrotation with myofibromas or hamartomas (summary by Twigg et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/167083">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_322167"><div><strong>Craniosynostosis 4</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>322167</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.">C1833340</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Craniosynostosis (CRS) is a primary abnormality of skull growth involving premature fusion of the cranial sutures such that the growth velocity of the skull often cannot match that of the developing brain. This produces skull deformity and, in some cases, raises intracranial pressure, which must be treated promptly to avoid permanent neurodevelopmental disability (summary by Fitzpatrick, 2013). Craniosynostosis-4 (CRS4) includes lambdoid, sagittal, metopic, coronal, and multisuture forms. For a discussion of genetic heterogeneity of craniosynostosis, see CRS1 (123100).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/322167">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_346753"><div><strong>Craniosynostosis 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>346753</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.">C1858160</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Craniosynostosis is a primary abnormality of skull growth involving premature fusion of the cranial sutures such that the growth velocity of the skull often cannot match that of the developing brain. This produces skull deformity and, in some cases, raises intracranial pressure, which must be treated promptly to avoid permanent neurodevelopmental disability (summary by Fitzpatrick, 2013). For a discussion of genetic heterogeneity of craniosynostosis, see CRS1 (123100).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/346753">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_811568"><div><strong>TCF12-related craniosynostosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>811568</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.">C3715051</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Craniosynostosis (CRS) is a primary abnormality of skull growth involving premature fusion of the cranial sutures such that the growth velocity of the skull often cannot match that of the developing brain. This produces skull deformity and, in some cases, raises intracranial pressure, which must be treated promptly to avoid permanent neurodevelopmental disability (summary by Fitzpatrick, 2013). Craniosynostosis-3 (CRS3) includes coronal, sagittal, and multisuture forms (Sharma et al., 2013). For discussion of genetic heterogeneity of craniosynostosis, see CRS1 (123100).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/811568">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_904675"><div><strong>Craniosynostosis 6</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>904675</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.">C4225269</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Craniosynostosis is a primary abnormality of skull growth involving premature fusion of the cranial sutures such that the growth velocity of the skull often cannot match that of the developing brain. This produces skull deformity and, in some cases, raises intracranial pressure, which must be treated promptly to avoid permanent neurodevelopmental disability (summary by Fitzpatrick, 2013). Craniosynostosis-6 (CRS6) is a bicoronal form associated with bony defects in the sagittal, metopic, or lambdoid sutures (Twigg et al., 2015). For a discussion of genetic heterogeneity of craniosynostosis, see CRS1 (123100).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/904675">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684861"><div><strong>Structural brain anomalies with impaired intellectual development and craniosynostosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684861</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.">C5231485</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Patients with BAIDCS have small head circumference with abnormalities in brain anatomy including variable deficiency of the corpus callosum (including agenesis), abnormal conformation of the ventricles and posterior fossa, hypoplasia of both cerebellar hemispheres, colpocephaly, and partial rhombencephalosynapsis (absence of the cerebellar vermis with fusion of the cerebellar hemispheres). Intellectual development is moderately to severely impaired. Bicoronal synostosis, scoliosis, and tethered cord may be present (Twigg et al., 2015; Vandervore et al., 2018). Craniosynostosis-6 (CRS6; 616602) is an allelic disorder.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684861">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1782253"><div><strong>Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1782253</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.">C5543057</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies-2 (SSFSC2) is characterized by thin and short long bones, distinctive facial dysmorphism, and dental and skeletal abnormalities, in the absence of developmental delay or intellectual disability. Cardiac anomalies have been reported in some patients (Lin et al., 2021). For a discussion of genetic heterogeneity of SSFSC, see SSFSC1 (617877).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1782253">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1811919"><div><strong>Hypogonadotropic hypogonadism 26 with or without anosmia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1811919</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.">C5676903</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">HH26 is characterized by micropenis and cryptorchidism at birth in male patients, and absent puberty and anosmia in male or female patients. Some affected individuals also exhibit craniosynostosis (Davis et al., 2020). Congenital idiopathic hypogonadotropic hypogonadism (IHH) is a disorder characterized by absent or incomplete sexual maturation by the age of 18 years, in conjunction with low levels of circulating gonadotropins and testosterone and no other abnormalities of the hypothalamic-pituitary axis. Idiopathic hypogonadotropic hypogonadism can be caused by an isolated defect in gonadotropin-releasing hormone (GNRH; 152760) release, action, or both. Other associated nonreproductive phenotypes, such as anosmia, cleft palate, and sensorineural hearing loss, occur with variable frequency. In the presence of anosmia, idiopathic hypogonadotropic hypogonadism has been called 'Kallmann syndrome (KS),' whereas in the presence of a normal sense of smell, it has been termed 'normosmic idiopathic hypogonadotropic hypogonadism (nIHH)' (summary by Raivio et al., 2007). Because families have been found to segregate both KS and nIHH, the disorder is here referred to as 'hypogonadotropic hypogonadism with or without anosmia (HH).' For a discussion of genetic heterogeneity of hypogonadotropic hypogonadism with or without anosmia as well as a discussion of oligogenicity of this disorder, see 147950.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1811919">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1804234"><div><strong>Tessadori-Van Haaften neurodevelopmental syndrome 4</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1804234</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.">C5677016</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Tessadori-Bicknell-van Haaften neurodevelopmental syndrome-4 (TEBIVANED4) is characterized by global developmental delay with poor overall growth, variably impaired intellectual development, learning difficulties, distal skeletal anomalies, and dysmorphic facies. Some patients have visual or hearing deficits. The severity and manifestations of the disorder are highly variable (Tessadori et al., 2022). For a discussion of genetic heterogeneity of TEBIVANED, see TEBIVANED1 (619758).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1804234">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_120532" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Baller-Gerold syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_346753" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Craniosynostosis 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_322167" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Craniosynostosis 4</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_904675" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Craniosynostosis 6</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_167083" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Curry-Jones syndrome</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (10)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1811919" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypogonadotropic hypogonadism 26 with or without anosmia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1782253" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684861" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Structural brain anomalies with impaired intellectual development and craniosynostosis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_811568" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">TCF12-related craniosynostosis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1804234" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Tessadori-Van Haaften neurodevelopmental syndrome 4</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33904513">Neurodevelopmental, Cognitive, and Psychosocial Outcomes for Individuals With Pathogenic Variants in the TCF12 Gene and Associated Craniosynostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kennedy-Williams P,
|
||
Care H,
|
||
Dalton L,
|
||
Horton J,
|
||
Kearney A,
|
||
Rooney N,
|
||
Hotton M,
|
||
Pinckston M,
|
||
Huggons E,
|
||
Culshaw L,
|
||
Kilcoyne S,
|
||
Johnson D,
|
||
Wilkie AOM,
|
||
Wall S</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2021 May 1;32(Suppl 3):1263-1268.
|
||
doi: 10.1097/SCS.0000000000007535.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33904513" target="_blank">33904513</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32398550">Management of Paronychia in Patients With Apert Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kim JS,
|
||
Block LM,
|
||
Zhu X,
|
||
Davit AJ</span><br />
|
||
<span class="medgenPMjournal">Tech Hand Up Extrem Surg</span>
|
||
2020 May 8;25(1):30-34.
|
||
doi: 10.1097/BTH.0000000000000295.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32398550" target="_blank">32398550</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(bicoronal%20synostosis)%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 (2)</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/35286288">Influence of Nonsyndromic Bicoronal Synostosis and Syndromic Influences on Orbit and Periorbital Malformation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lu X,
|
||
Forte AJ,
|
||
Dinis J,
|
||
Junn A,
|
||
Alperovich M,
|
||
Alonso N,
|
||
Persing JA</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2022 May 1;149(5):930e-942e.
|
||
Epub 2022 Mar 14
|
||
doi: 10.1097/PRS.0000000000009051.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35286288" target="_blank">35286288</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34181610">Respective Roles of Craniosynostosis and Syndromic Influences on Cranial Fossa Development.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lu X,
|
||
Forte AJ,
|
||
Wilson AT,
|
||
Park KE,
|
||
Allam O,
|
||
Alperovich M,
|
||
Steinbacher DM,
|
||
Alonso N,
|
||
Persing JA</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2021 Jul 1;148(1):145-156.
|
||
doi: 10.1097/PRS.0000000000008101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34181610" target="_blank">34181610</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31525394">What remains of non-syndromic bicoronal synostosis?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vinchon M</span><br />
|
||
<span class="medgenPMjournal">Neurochirurgie</span>
|
||
2019 Nov;65(5):252-257.
|
||
Epub 2019 Sep 13
|
||
doi: 10.1016/j.neuchi.2019.09.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31525394" target="_blank">31525394</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30074960">Staged Raising of a Coronal Flap for Fronto-Orbital Advancement and Remodeling in Saethre-Chotzen Syndrome Complicated by Sinus Pericranii.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shaw AV,
|
||
Jayamohan J,
|
||
Sheerin F,
|
||
Johnson D</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2018 Oct;29(7):1956-1959.
|
||
doi: 10.1097/SCS.0000000000004786.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30074960" target="_blank">30074960</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/19483581">Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Woods RH,
|
||
Ul-Haq E,
|
||
Wilkie AOM,
|
||
Jayamohan J,
|
||
Richards PG,
|
||
Johnson D,
|
||
Lester T,
|
||
Wall SA</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2009 Jun;123(6):1801-1810.
|
||
doi: 10.1097/PRS.0b013e3181a3f391.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19483581" target="_blank">19483581</a><a href="/pmc/articles/PMC2719244" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bicoronal%20synostosis%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 (32)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34181610">Respective Roles of Craniosynostosis and Syndromic Influences on Cranial Fossa Development.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lu X,
|
||
Forte AJ,
|
||
Wilson AT,
|
||
Park KE,
|
||
Allam O,
|
||
Alperovich M,
|
||
Steinbacher DM,
|
||
Alonso N,
|
||
Persing JA</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2021 Jul 1;148(1):145-156.
|
||
doi: 10.1097/PRS.0000000000008101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34181610" target="_blank">34181610</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32842109">What Is the Difference in Cranial Base Morphology in Isolated and Syndromic Bicoronal Synostosis?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lu X,
|
||
Forte AJ,
|
||
Wilson AT,
|
||
Park KE,
|
||
Allam O,
|
||
Mozaffari MA,
|
||
Alperovich M,
|
||
Steinbacher DM,
|
||
Alonso N,
|
||
Persing JA</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2020 Sep;146(3):599-610.
|
||
doi: 10.1097/PRS.0000000000007068.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32842109" target="_blank">32842109</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31525394">What remains of non-syndromic bicoronal synostosis?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vinchon M</span><br />
|
||
<span class="medgenPMjournal">Neurochirurgie</span>
|
||
2019 Nov;65(5):252-257.
|
||
Epub 2019 Sep 13
|
||
doi: 10.1016/j.neuchi.2019.09.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31525394" target="_blank">31525394</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22691840">Analysis of the long-term outcomes of nonsyndromic bicoronal synostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bastidas N,
|
||
Mackay DDJ,
|
||
Taylor JA,
|
||
Bartlett SP</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2012 Oct;130(4):877-883.
|
||
doi: 10.1097/PRS.0b013e318262f2fd.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22691840" target="_blank">22691840</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9780908">Bilambdoid and posterior sagittal synostosis: the Mercedes Benz syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Moore MH,
|
||
Abbott AH,
|
||
Netherway DJ,
|
||
Menard R,
|
||
Hanieh A</span><br />
|
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<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
1998 Sep;9(5):417-22.
|
||
doi: 10.1097/00001665-199809000-00003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9780908" target="_blank">9780908</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bicoronal%20synostosis%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 (21)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30640858">Evaluation of Endoscopic Strip Craniectomy and Orthotic Therapy for Bilateral Coronal Craniosynostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Williams CT,
|
||
Segar DJ,
|
||
Naidoo SD,
|
||
Skolnick GB,
|
||
Proctor MR,
|
||
Smyth MD,
|
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Patel KB</span><br />
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<span class="medgenPMjournal">J Craniofac Surg</span>
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2019 Mar/Apr;30(2):453-457.
|
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doi: 10.1097/SCS.0000000000005118.
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<span class="bold">PMID: </span><a href="/pubmed/30640858" target="_blank">30640858</a><a href="/pmc/articles/PMC6541507" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22872251">The Christmas tree foreheadplasty: a novel technique used in combination with a bandeau for fronto-orbital remodelling in craniosynostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Britto JA,
|
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Gwanmesia I,
|
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Leshem D</span><br />
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<span class="medgenPMjournal">Childs Nerv Syst</span>
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2012 Sep;28(9):1375-80.
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Epub 2012 Aug 8
|
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||
<span class="bold">PMID: </span><a href="/pubmed/22872251" target="_blank">22872251</a></div>
|
||
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||
<div class="nl"><a target="_blank" href="/pubmed/22691840">Analysis of the long-term outcomes of nonsyndromic bicoronal synostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bastidas N,
|
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Mackay DDJ,
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Taylor JA,
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Bartlett SP</span><br />
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<span class="medgenPMjournal">Plast Reconstr Surg</span>
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2012 Oct;130(4):877-883.
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doi: 10.1097/PRS.0b013e318262f2fd.
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<span class="bold">PMID: </span><a href="/pubmed/22691840" target="_blank">22691840</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21311385">Long-term outcomes of primary craniofacial reconstruction for craniosynostosis: a 12-year experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Seruya M,
|
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Oh AK,
|
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Boyajian MJ,
|
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Posnick JC,
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Myseros JS,
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Yaun AL,
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Keating RF</span><br />
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<span class="medgenPMjournal">Plast Reconstr Surg</span>
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2011 Jun;127(6):2397-2406.
|
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doi: 10.1097/PRS.0b013e318213a178.
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<span class="bold">PMID: </span><a href="/pubmed/21311385" target="_blank">21311385</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bicoronal%20synostosis%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 (4)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31525394">What remains of non-syndromic bicoronal synostosis?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vinchon M</span><br />
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<span class="medgenPMjournal">Neurochirurgie</span>
|
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2019 Nov;65(5):252-257.
|
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Epub 2019 Sep 13
|
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doi: 10.1016/j.neuchi.2019.09.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31525394" target="_blank">31525394</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30640858">Evaluation of Endoscopic Strip Craniectomy and Orthotic Therapy for Bilateral Coronal Craniosynostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Williams CT,
|
||
Segar DJ,
|
||
Naidoo SD,
|
||
Skolnick GB,
|
||
Proctor MR,
|
||
Smyth MD,
|
||
Patel KB</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2019 Mar/Apr;30(2):453-457.
|
||
doi: 10.1097/SCS.0000000000005118.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30640858" target="_blank">30640858</a><a href="/pmc/articles/PMC6541507" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29290519">Reduced Intercarotid Artery Distance in Syndromic and Isolated Brachycephaly.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Assadsangabi R,
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Hajmomenian M,
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Nabavizadeh SA,
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Schmitt JE,
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Vossough A</span><br />
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<span class="medgenPMjournal">Pediatr Neurol</span>
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2018 Feb;79:3-7.
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Epub 2017 Oct 9
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doi: 10.1016/j.pediatrneurol.2017.09.018.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29290519" target="_blank">29290519</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22872251">The Christmas tree foreheadplasty: a novel technique used in combination with a bandeau for fronto-orbital remodelling in craniosynostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Britto JA,
|
||
Gwanmesia I,
|
||
Leshem D</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2012 Sep;28(9):1375-80.
|
||
Epub 2012 Aug 8
|
||
doi: 10.1007/s00381-012-1806-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22872251" target="_blank">22872251</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3469040">Skull morphology after early craniotomy in patients with premature synostosis of the coronal suture.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Friede H,
|
||
Lilja J,
|
||
Lauritzen C,
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||
Andersson H,
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Johanson B</span><br />
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<span class="medgenPMjournal">Cleft Palate J</span>
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||
1986 Dec;23 Suppl 1:1-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3469040" target="_blank">3469040</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bicoronal%20synostosis%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 (15)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37322751">Introduction of Spring-Assisted Cranioplasty for Bicoronal Synotosis in India: Description of First Case and Our Learning Experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chattopadhyay D,
|
||
Vathulya M,
|
||
Kapoor A,
|
||
Arora R</span><br />
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||
<span class="medgenPMjournal">Neurol India</span>
|
||
2023 May-Jun;71(3):527-530.
|
||
doi: 10.4103/0028-3886.378708.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37322751" target="_blank">37322751</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35286288">Influence of Nonsyndromic Bicoronal Synostosis and Syndromic Influences on Orbit and Periorbital Malformation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lu X,
|
||
Forte AJ,
|
||
Dinis J,
|
||
Junn A,
|
||
Alperovich M,
|
||
Alonso N,
|
||
Persing JA</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2022 May 1;149(5):930e-942e.
|
||
Epub 2022 Mar 14
|
||
doi: 10.1097/PRS.0000000000009051.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35286288" target="_blank">35286288</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25686894">Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Assadsangabi R,
|
||
Hajmomenian M,
|
||
Bilaniuk LT,
|
||
Vossough A</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2015 May;31(5):735-41.
|
||
Epub 2015 Feb 17
|
||
doi: 10.1007/s00381-015-2639-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25686894" target="_blank">25686894</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22777440">Spring-assisted cranioplasty for bicoronal synostosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tovetjärn R,
|
||
Maltese G,
|
||
Kölby L,
|
||
Kreiborg S,
|
||
Tarnow P</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2012 Jul;23(4):977-81.
|
||
doi: 10.1097/SCS.0b013e31824e2bec.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22777440" target="_blank">22777440</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17036334">Trigonocephaly in Muenke syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van der Meulen J,
|
||
van den Ouweland A,
|
||
Hoogeboom J</span><br />
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||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2006 Nov 15;140(22):2493-4.
|
||
doi: 10.1002/ajmg.a.31460.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17036334" target="_blank">17036334</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Bicoronal%20synostosis%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 (15)</a></div></div>
|
||
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|
||
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|
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|
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|
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<div class="supplemental col three_col last">
|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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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=(bicoronal%20synostosis)%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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</div>
|
||
<div class="row">
|
||
<div class="col-lg-12 centered-lg">
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||
<nav class="bottom-links">
|
||
<ul class="mt-3">
|
||
<li>
|
||
<a class="text-white" href="//www.nlm.nih.gov/">NLM</a>
|
||
</li>
|
||
<li>
|
||
<a class="text-white" href="https://www.nih.gov/">NIH</a>
|
||
</li>
|
||
<li>
|
||
<a class="text-white" href="https://www.hhs.gov/">HHS</a>
|
||
</li>
|
||
<li>
|
||
<a class="text-white" href="https://www.usa.gov/">USA.gov</a>
|
||
</li>
|
||
</ul>
|
||
</nav>
|
||
</div>
|
||
</div>
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||
</div>
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||
</section>
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<script type="text/javascript" src="/portal/portal3rc.fcgi/rlib/js/InstrumentOmnitureBaseJS/InstrumentNCBIConfigJS/InstrumentNCBIBaseJS/InstrumentPageStarterJS.js?v=1"> </script>
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<script type="text/javascript" src="/portal/portal3rc.fcgi/static/js/hfjs2.js"> </script>
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</div>
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</div>
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||
|
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