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<meta name="keywords" content="C1861443, facial hemangioma, facial hemangiomata, finding, 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="Hemangioma, a benign tumor of the vascular endothelial cells, occurring in the face." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=348361
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ConceptID=C1861443
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Facial hemangioma</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>348361</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C1861443</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Facial hemangiomata</td></tr>
|
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<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0000329">HP:0000329</a></td></tr>
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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">Hemangioma, a benign tumor of the vascular endothelial cells, occurring in the face. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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<div 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">Facial hemangioma</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/867442" ref="tree=MeSH" title="MedGen record for Abnormality of head or neck">Abnormality of head or neck</a></span><ul><li><span class="TLline"><a href="/medgen/867438" ref="tree=MeSH" title="MedGen record for Abnormality of the head">Abnormality of the head</a></span><ul><li><span class="TLline"><a href="/medgen/871375" ref="tree=MeSH" title="MedGen record for Abnormality of the face">Abnormality of the face</a></span><ul><li><span class="TLline"><a href="/medgen/868778" ref="tree=MeSH" title="MedGen record for Abnormality of facial soft tissue">Abnormality of facial soft tissue</a></span><ul><li><span class="matched_ds">Facial hemangioma</span><ul><li><span class="TLline"><a href="/medgen/350686" ref="tree=MeSH" title="MedGen record for Facial midline hemangioma">Facial midline hemangioma</a></span></li><li><span class="TLline"><a href="/medgen/376233" ref="tree=MeSH" title="MedGen record for Plaque-like facial hemangioma">Plaque-like facial hemangioma</a></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>
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<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_21361"><div><strong>Sturge-Weber syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>21361</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.">C0038505</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Sturge-Weber syndrome (SWS) is characterized by an intracranial vascular anomaly, leptomeningeal angiomatosis, most often involving the occipital and posterior parietal lobes. The most common symptoms and signs are facial cutaneous vascular malformations (port-wine stains), seizures, and glaucoma. Stasis results in ischemia underlying the leptomeningeal angiomatosis, leading to calcification and laminar cortical necrosis. The clinical course is highly variable and some children experience intractable seizures, mental retardation, and recurrent stroke-like episodes (review by Thomas-Sohl et al., 2004).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/21361">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_120517"><div><strong>Schinzel-Giedion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>120517</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.">C0265227</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Classic Schinzel-Giedion syndrome (SGS), an ultra-rare multisystem disorder caused by gain-of-function pathogenic variants in a SETBP1 mutational hot spot, is characterized by global neurodevelopmental impairment leading to moderate-to-profound intellectual disability, epilepsy (often refractory to treatment), hypotonia, spasticity, dysautonomia, hearing loss, and cerebral visual impairment. Other findings can include poor weight gain often associated with gastroesophageal reflux disease, chronic vomiting, constipation, gastroparesis, and/or feeding intolerance. Structural malformations can involve the heart, skeleton, kidney and urinary tract, genitalia, and brain. Anomalies of the liver, spleen, and/or pancreas are less common. Other features may include neuroepithelial neoplasia, severely disrupted sleep, choanal stenosis, inguinal hernia, sensitive skin, and increased risk of infection. To date, more than 50 individuals have been reported with molecularly confirmed classic SGS. Atypical SGS, reported in five individuals to date, is caused by pathogenic SETBP1 variants in proximity to – but not within – the mutational hot spot. The broad spectrum of clinical features of variable severity partially overlaps with classic SGS; however, this spectrum does not include risk for neuroepithelial neoplasia to date.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/120517">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_208678"><div><strong>Bohring-Opitz syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>208678</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.">C0796232</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Bohring-Opitz syndrome (BOS) is characterized by distinctive facial features and posture, growth failure, variable but usually severe intellectual disability, and variable anomalies. The facial features may include microcephaly or trigonocephaly / prominent (but not fused) metopic ridge, hypotonic facies with full cheeks, synophrys, glabellar and eyelid nevus flammeus (simplex), prominent globes, widely set eyes, palate anomalies, and micrognathia. The BOS posture, which is most striking in early childhood and often becomes less apparent with age, is characterized by flexion at the elbows with ulnar deviation and flexion of the wrists and metacarpophalangeal joints. Feeding difficulties in early childhood, including cyclic vomiting, have a significant impact on overall health; feeding tends to improve with age. Seizures are common and typically responsive to standard epileptic medications. Minor cardiac anomalies and transient bradycardia and apnea may be present. Affected individuals may experience recurrent infections, which also tend to improve with age. Isolated case reports suggest that individuals with BOS are at greater risk for Wilms tumor than the general population, but large-scale epidemiologic studies have not been conducted.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/208678">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_376231"><div><strong>PHACE syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>376231</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.">C1847874</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">PHACE is an acronym for a neurocutaneous syndrome encompassing the following features: posterior fossa brain malformations, hemangiomas of the face (large or complex), arterial anomalies, cardiac anomalies, and eye abnormalities. The association is referred to as PHACES when ventral developmental defects, such as sternal clefting or supraumbilical raphe, are present (summary by Bracken et al., 2011).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/376231">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_350477"><div><strong>Rubinstein-Taybi syndrome due to 16p13.3 microdeletion</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>350477</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.">C1864648</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Chromosome 16p13.3deletion syndrome is a chromosome abnormality that can affect many parts of the body. People with this condition are missing a small piece (deletion) of chromosome 16 at a location designated p13.3. Although once thought to be a severe form of Rubinstein-Taybi syndrome, it is now emerging as a unique syndrome. Signs and symptoms may include failure to thrive, hypotonia (reduced muscle tone), short stature, microcephaly (unusually small head), characteristic facial features, mild to moderate intellectual disability, organ anomalies (i.e. heart and/or kidney problems), and vulnerability to infections. Chromosome testing of both parents can provide information about whether the deletion was inherited. In most cases, parents do not have any chromosome abnormalities. However, sometimes one parent has a balanced translocation where a piece of a chromosome has broken off and attached to another one with no gain or loss of genetic material. The balanced translocation normally does not cause signs or symptoms, but it increases the risk for having a child with a chromosome abnormality like a deletion. Treatment is based on the signs and symptoms present in each person.To learn more about chromosome abnormalities in general, view our GARD fact sheet on Chromosome Disorders.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/350477">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_382543"><div><strong>Kahrizi syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>382543</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.">C2675185</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Kahrizi syndrome is an autosomal recessive neurodevelopmental disorder characterized by mental retardation, cataracts, coloboma, kyphosis, and coarse facial features (summary by Kahrizi et al., 2009). See also congenital disorder of glycosylation type Iq (CDG1Q; 612379), an allelic disorder with overlapping features.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/382543">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1376945"><div><strong>Noonan syndrome-like disorder with loose anagen hair 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1376945</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.">C4479577</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An inherited condition caused by autosomal dominant mutation(s) in the PPP1CB gene, encoding serine/threonine-protein phosphatase PP1-beta catalytic subunit. The condition is characterized by facial features similar to those seen in Noonan syndrome but may also include short stature, cognitive deficits, relative macrocephaly, small posterior fossa resulting in Chiari I malformation, hypernasal voice, cardiac defects, and ectodermal abnormalities, which typically presents as slow-growing, sparse, and/or unruly hair.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1376945">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_208678" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Bohring-Opitz syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_382543" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Kahrizi syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1376945" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Noonan syndrome-like disorder with loose anagen hair 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_376231" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">PHACE syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_350477" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Rubinstein-Taybi syndrome due to 16p13.3 microdeletion</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_120517" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Schinzel-Giedion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_21361" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Sturge-Weber syndrome</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37953576">Efficacy of timolol in the treatment of facial hemangioma and its effect on the proliferation and apoptosis of hemangioma stem cells.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhu H,
|
||
Luo H,
|
||
Lai W</span><br />
|
||
<span class="medgenPMjournal">Cell Mol Biol (Noisy-le-grand)</span>
|
||
2023 Oct 31;69(10):115-120.
|
||
doi: 10.14715/cmb/2023.69.10.16.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37953576" target="_blank">37953576</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28064423">Pathophysiology, diagnosis, and management of glaucoma associated with Sturge-Weber syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Javaid U,
|
||
Ali MH,
|
||
Jamal S,
|
||
Butt NH</span><br />
|
||
<span class="medgenPMjournal">Int Ophthalmol</span>
|
||
2018 Feb;38(1):409-416.
|
||
Epub 2017 Jan 7
|
||
doi: 10.1007/s10792-016-0412-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28064423" target="_blank">28064423</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4636496">Treatment of facial hemangioma by intravascular embolization with silicone spheres. Case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Longacre JJ,
|
||
Benton C,
|
||
Unterthiner RA</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
1972 Dec;50(6):618-21.
|
||
doi: 10.1097/00006534-197212000-00019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4636496" target="_blank">4636496</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22facial%20hemangioma%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 (7)</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/37953576">Efficacy of timolol in the treatment of facial hemangioma and its effect on the proliferation and apoptosis of hemangioma stem cells.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhu H,
|
||
Luo H,
|
||
Lai W</span><br />
|
||
<span class="medgenPMjournal">Cell Mol Biol (Noisy-le-grand)</span>
|
||
2023 Oct 31;69(10):115-120.
|
||
doi: 10.14715/cmb/2023.69.10.16.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37953576" target="_blank">37953576</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36084212">Feasible Removal of Facial Hemangiomas Under Local Anesthesia in Young Children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hazkour N,
|
||
Palacios J,
|
||
Othman S,
|
||
Smith JD,
|
||
Goote P,
|
||
Bastidas N</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2023 Jan-Feb 01;34(1):356-357.
|
||
Epub 2022 Sep 9
|
||
doi: 10.1097/SCS.0000000000008993.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36084212" target="_blank">36084212</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34036811">PHACES Syndrome and Associated Anomalies: Risk Associated With Small and Large Facial Hemangiomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Proisy M,
|
||
Powell J,
|
||
McCuaig C,
|
||
Jalbout RE,
|
||
Lapierre C,
|
||
Dubois J</span><br />
|
||
<span class="medgenPMjournal">AJR Am J Roentgenol</span>
|
||
2021 Aug;217(2):507-514.
|
||
Epub 2021 May 26
|
||
doi: 10.2214/AJR.20.23488.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34036811" target="_blank">34036811</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30421264">Clinical and economic impact of surgery for treating infantile hemangiomas in the era of propranolol: overview of single-center experience from La Paz Hospital, Madrid.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">López-Gutiérrez JC</span><br />
|
||
<span class="medgenPMjournal">Eur J Pediatr</span>
|
||
2019 Jan;178(1):1-6.
|
||
Epub 2018 Nov 12
|
||
doi: 10.1007/s00431-018-3290-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30421264" target="_blank">30421264</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11445804">The many faces of PHACE syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Metry DW,
|
||
Dowd CF,
|
||
Barkovich AJ,
|
||
Frieden IJ</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2001 Jul;139(1):117-23.
|
||
doi: 10.1067/mpd.2001.114880.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11445804" target="_blank">11445804</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Facial%20hemangioma%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 (24)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39746540">Contralateral oculomotor nerve palsy associated with PHACES syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yu S,
|
||
Mulholland C</span><br />
|
||
<span class="medgenPMjournal">J AAPOS</span>
|
||
2025 Feb;29(1):104094.
|
||
Epub 2024 Dec 31
|
||
doi: 10.1016/j.jaapos.2024.104094.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39746540" target="_blank">39746540</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27977032">Multiple Pathological Ocular Findings in a Patient With PHACE Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Biler ED,
|
||
Uretmen O</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Ophthalmol Strabismus</span>
|
||
2016 Dec 8;53:e72-e74.
|
||
doi: 10.3928/01913913-20161102-03.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27977032" target="_blank">27977032</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10976488">Ultrasonographic detection of fetal cranio-facial hemangioma: case report and review of the literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Viora E,
|
||
Grassi Pirrone P,
|
||
Comoglio F,
|
||
Bastonero S,
|
||
Campogrande M</span><br />
|
||
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
|
||
2000 May;15(5):431-4.
|
||
doi: 10.1046/j.1469-0705.2000.00117.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10976488" target="_blank">10976488</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3531547">Prenatal sonographic diagnosis of a fetal facial hemangioma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pennell RG,
|
||
Baltarowich OH</span><br />
|
||
<span class="medgenPMjournal">J Ultrasound Med</span>
|
||
1986 Sep;5(9):525-8.
|
||
doi: 10.7863/jum.1986.5.9.525.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3531547" target="_blank">3531547</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/5033248">Hypomelia-hypotrichosis-facial hemangioma syndrome (pseudothalidomide, SC syndrome, SC phocomelia syndrome).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hall BD,
|
||
Greenberg MH</span><br />
|
||
<span class="medgenPMjournal">Am J Dis Child</span>
|
||
1972 Jun;123(6):602-4.
|
||
doi: 10.1001/archpedi.1972.02110120126020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/5033248" target="_blank">5033248</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Facial%20hemangioma%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 (43)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37953576">Efficacy of timolol in the treatment of facial hemangioma and its effect on the proliferation and apoptosis of hemangioma stem cells.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhu H,
|
||
Luo H,
|
||
Lai W</span><br />
|
||
<span class="medgenPMjournal">Cell Mol Biol (Noisy-le-grand)</span>
|
||
2023 Oct 31;69(10):115-120.
|
||
doi: 10.14715/cmb/2023.69.10.16.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37953576" target="_blank">37953576</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30421264">Clinical and economic impact of surgery for treating infantile hemangiomas in the era of propranolol: overview of single-center experience from La Paz Hospital, Madrid.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">López-Gutiérrez JC</span><br />
|
||
<span class="medgenPMjournal">Eur J Pediatr</span>
|
||
2019 Jan;178(1):1-6.
|
||
Epub 2018 Nov 12
|
||
doi: 10.1007/s00431-018-3290-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30421264" target="_blank">30421264</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3343574">Thyroid carcinoma, cataract and hearing loss in a patient after irradiation for facial hemangioma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Talmi Y,
|
||
Kalmanovitch M,
|
||
Zohar Y</span><br />
|
||
<span class="medgenPMjournal">J Laryngol Otol</span>
|
||
1988 Jan;102(1):91-2.
|
||
doi: 10.1017/s0022215100104086.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3343574" target="_blank">3343574</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4636496">Treatment of facial hemangioma by intravascular embolization with silicone spheres. Case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Longacre JJ,
|
||
Benton C,
|
||
Unterthiner RA</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
1972 Dec;50(6):618-21.
|
||
doi: 10.1097/00006534-197212000-00019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4636496" target="_blank">4636496</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/5368330">Thrombocytopenia in a patient with a relatively small facial hemangioma. Successful management with irradiation after failure of prednisone therapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Corby DG,
|
||
Oquendo-Cabrera A,
|
||
Louro JM</span><br />
|
||
<span class="medgenPMjournal">Clin Pediatr (Phila)</span>
|
||
1969 Dec;8(12):728-31.
|
||
doi: 10.1177/000992286900801213.
|
||
<span class="bold">PMID: </span><a href="/pubmed/5368330" target="_blank">5368330</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Facial%20hemangioma%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 (16)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30421264">Clinical and economic impact of surgery for treating infantile hemangiomas in the era of propranolol: overview of single-center experience from La Paz Hospital, Madrid.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">López-Gutiérrez JC</span><br />
|
||
<span class="medgenPMjournal">Eur J Pediatr</span>
|
||
2019 Jan;178(1):1-6.
|
||
Epub 2018 Nov 12
|
||
doi: 10.1007/s00431-018-3290-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30421264" target="_blank">30421264</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27389245">Megalencephalic leukoencephalopathy with cysts in twelve Egyptian patients: novel mutations in MLC1 and HEPACAM and a founder effect.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Abdel-Salam GM,
|
||
Abdel-Hamid MS,
|
||
Ismail SI,
|
||
Hosny H,
|
||
Omar T,
|
||
Effat L,
|
||
Aglan MS,
|
||
Temtamy SA,
|
||
Zaki MS</span><br />
|
||
<span class="medgenPMjournal">Metab Brain Dis</span>
|
||
2016 Oct;31(5):1171-9.
|
||
Epub 2016 Jul 7
|
||
doi: 10.1007/s11011-016-9861-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27389245" target="_blank">27389245</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18261600">Pregnancy after renal transplantation: ten-year single-center experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ghafari A,
|
||
Sanadgol H</span><br />
|
||
<span class="medgenPMjournal">Transplant Proc</span>
|
||
2008 Jan-Feb;40(1):251-2.
|
||
doi: 10.1016/j.transproceed.2007.11.052.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18261600" target="_blank">18261600</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14996395">Segmental facial hemangioma accompanied by brain anomalies: report of a case.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Douri T</span><br />
|
||
<span class="medgenPMjournal">Dermatol Online J</span>
|
||
2003 Dec;9(5):22.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14996395" target="_blank">14996395</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9481012">Growing up with a facial hemangioma: parent and child coping and adaptation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tanner JL,
|
||
Dechert MP,
|
||
Frieden IJ</span><br />
|
||
<span class="medgenPMjournal">Pediatrics</span>
|
||
1998 Mar;101(3 Pt 1):446-52.
|
||
doi: 10.1542/peds.101.3.446.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9481012" target="_blank">9481012</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Facial%20hemangioma%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 (11)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37953576">Efficacy of timolol in the treatment of facial hemangioma and its effect on the proliferation and apoptosis of hemangioma stem cells.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhu H,
|
||
Luo H,
|
||
Lai W</span><br />
|
||
<span class="medgenPMjournal">Cell Mol Biol (Noisy-le-grand)</span>
|
||
2023 Oct 31;69(10):115-120.
|
||
doi: 10.14715/cmb/2023.69.10.16.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37953576" target="_blank">37953576</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32610335">Epidemiology, Clinical Features, and Use of Early Supportive Measures in PHACE Syndrome: A European Multinational Observational Study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Disse SC,
|
||
Toelle SP,
|
||
Schroeder S,
|
||
Theiler M,
|
||
Weibel L,
|
||
Broser P,
|
||
Langner C,
|
||
Siegel D,
|
||
Brockmann K,
|
||
Schoenfelder I,
|
||
Meyer S</span><br />
|
||
<span class="medgenPMjournal">Neuroepidemiology</span>
|
||
2020;54(5):383-391.
|
||
Epub 2020 Jul 1
|
||
doi: 10.1159/000508187.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32610335" target="_blank">32610335</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29171184">Structural malformations of the brain, eye, and pituitary gland in PHACE syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Steiner JE,
|
||
McCoy GN,
|
||
Hess CP,
|
||
Dobyns WB,
|
||
Metry DW,
|
||
Drolet BA,
|
||
Maheshwari M,
|
||
Siegel DH</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2018 Jan;176(1):48-55.
|
||
Epub 2017 Nov 24
|
||
doi: 10.1002/ajmg.a.38523.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29171184" target="_blank">29171184</a><a href="/pmc/articles/PMC5844264" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14699619">Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Grosso S,
|
||
De Cosmo L,
|
||
Bonifazi E,
|
||
Galluzzi P,
|
||
Farnetani MA,
|
||
Loffredo P,
|
||
Anichini C,
|
||
Berardi R,
|
||
Morgese G,
|
||
Balestri P</span><br />
|
||
<span class="medgenPMjournal">Am J Med Genet A</span>
|
||
2004 Jan 15;124A(2):192-5.
|
||
doi: 10.1002/ajmg.a.20316.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14699619" target="_blank">14699619</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9481012">Growing up with a facial hemangioma: parent and child coping and adaptation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tanner JL,
|
||
Dechert MP,
|
||
Frieden IJ</span><br />
|
||
<span class="medgenPMjournal">Pediatrics</span>
|
||
1998 Mar;101(3 Pt 1):446-52.
|
||
doi: 10.1542/peds.101.3.446.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9481012" target="_blank">9481012</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Facial%20hemangioma%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 (14)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
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<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/38823231">Stereotactic radiosurgery for facial nerve hemangioma: Case report and systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Park DJ,
|
||
Hori YS,
|
||
Nernekli K,
|
||
Persad AR,
|
||
Tayag A,
|
||
Ustrzynski L,
|
||
Emrich SC,
|
||
Hancock SL,
|
||
Chang SD</span><br />
|
||
<span class="medgenPMjournal">J Clin Neurosci</span>
|
||
2024 Aug;126:21-25.
|
||
Epub 2024 May 31
|
||
doi: 10.1016/j.jocn.2024.05.023.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38823231" target="_blank">38823231</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Facial%20hemangioma%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1)</a></div></div>
|
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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><li><a href="https://clinicaltrials.gov/search?cond=Facial%20hemangioma" target="_blank">ClinicalTrials.gov</a></li></ul></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=(%22facial%20hemangioma%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(%22Facial%20hemangioma%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 class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67ce9180a68b6b5afc60c552">Facial hemangioma</a>
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