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<meta name="keywords" content="C1849667, broad base of nose, broad nasal base, finding, increased width of base of nose, increased width of nasal base, wide base of nose, wide nasal base, 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="Increased distance between the attachments of the alae nasi to the face." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
|
||
UID=341506
|
||
ConceptID=C1849667
|
||
-->
|
||
<!--imgCountBooks = 0--><div class="ncbi_carousel" data-ncbicarousel-config="imageWidth:'100px',numItemsVisible:2,toggler:false"><div class="nc_header"><span class="img_strip_title">Image</span></div><div class="nc_content"><div class="nc_item"><a class="figpopup"><img alt="Figure 1" src="/projects/medgen/images/thumb/4a8c3cd977c27473.1.thumb.jpg" src-large="/projects/medgen/images/4a8c3cd977c27473.1.jpg" /></a><br /><a href="http://elementsofmorphology.nih.gov/index.cgi?tid=4a8c3cd977c27473" target="_blank" title="Elements of Morphology: Human Malformation Terminology - NHGRI">details</a></div></div></div><h1 class="medgenTitle"><div class="MedGenTitleText">Wide nasal base</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>341506</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:">C1849667</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Broad base of nose; Broad nasal base</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0012810">HP:0012810</a></td></tr>
|
||
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">Increased distance between the attachments of the alae nasi to 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>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1849667[DISCUI]&test_type=Clinical" ref="ncbi_uid=341506">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=341506" ref="ncbi_uid=341506">V</a></span></span><span class="TLline">Wide nasal base</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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/539457" ref="tree=MeSH" title="MedGen record for Abnormality of the nose">Abnormality of the nose</a></span><ul><li><span class="TLline"><a href="/medgen/870795" ref="tree=MeSH" title="MedGen record for Abnormal nasal morphology">Abnormal nasal morphology</a></span><ul><li><span class="TLline"><a href="/medgen/868324" ref="tree=MeSH" title="MedGen record for Abnormal nasal base norphology">Abnormal nasal base norphology</a></span><ul><li><span class="matched_ds">Wide nasal base</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_220983"><div><strong>Nicolaides-Baraitser syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>220983</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.">C1303073</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">SMARCA2-related Nicolaides-Baraitser syndrome (SMARCA2-NCBRS) is characterized by commonly shared dysmorphic features including sparse scalp hair, prominence of the interphalangeal joints and distal phalanges due to decreased subcutaneous fat, characteristic coarse facial features, microcephaly (typically acquired), seizures, and developmental delay / intellectual disability. Developmental delay / intellectual disability is severe in nearly half of affected individuals, moderate in one third, and mild in the remainder. Nearly one third never develop speech or language skills. Seizures are of various types and can be difficult to manage, requiring multiple anti-seizure medications to achieve reasonable control. Regression or lack of developmental progress has been noted with the onset of seizures in some affected individuals. Behavioral issues can include autistic-like features (perseveration, hyperacusis), with a minority of affected individuals being diagnosed clinically with an autism spectrum disorder. Cryptorchidism is common in males. About half of affected individuals have growth deficiency and short stature. Delayed tooth eruption with hypo- or oligodontia has also been reported. Radiographic findings may include cone-shaped epiphyses, metaphyseal flaring of the phalanges, and shortening of the phalanges, metacarpals, and/or metatarsals (especially of the 4th and 5th rays) of the hands; platyspondyly; flat intervertebral disc space; and pelvic/femoral anomalies. Rare findings include conductive hearing loss, refractive error / astigmatism, and congenital heart defects.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/220983">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_342675"><div><strong>Gingival fibromatosis-hypertrichosis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>342675</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.">C1851120</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Extreme hirsutism with gingival fibromatosis follows a dominant pattern of inheritance (Weski, 1920; Garn and Hatch, 1950). There is no necessary relationship between the age of development of the gingival changes and the hypertrichosis. The latter may be present at birth but often appears at puberty (Anderson et al., 1969). For a discussion of genetic heterogeneity of congenital generalized hypertrichosis, see HTC1 (145701).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/342675">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_816016"><div><strong>Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>816016</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3809686</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CTCF-related disorder is characterized by developmental delay / intellectual disability (ranging from mild to severe), with both speech and motor delays being common; feeding difficulties, including dysphagia, and other gastrointestinal issues (gastroesophageal reflux disease and/or irritable bowel syndrome) that can lead to growth deficiency; hypotonia; eye anomalies (strabismus and/or refractive errors); scoliosis; nonspecific dysmorphic features; sleep disturbance; tooth anomalies (crowded teeth and/or abnormal decay); and, less commonly, other congenital anomalies (cleft palate, gastrointestinal malrotation, genitourinary anomalies, and congenital heart defects, including aortic ectasia). Short stature, seizures, hearing loss, recurrent infections, microcephaly, and autistic features have also been described in a minority of affected individuals. At least four reported individuals with CTCF-related disorder developed Wilms tumor, one of whom had bilateral Wilms tumor. However, there is no clear evidence of a significant predisposition for the development of cancer in individuals with CTCF-related disorder at this time.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/816016">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_909304"><div><strong>Intellectual disability, autosomal dominant 39</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>909304</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.">C4225296</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An autosomal dominant condition caused by mutation(s) in the MYT1L gene, encoding myelin transcription factor 1-like protein. It is characterized by intellectual disability and mild dysmorphic facial features.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/909304">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1385755"><div><strong>Autosomal recessive cutis laxa type 2C</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1385755</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.">C4479387</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive cutis laxa type IIC (ARCL2C) is characterized by generalized skin wrinkling with sparse subcutaneous fat and dysmorphic progeroid facial features. Most patients also exhibit severe hypotonia as well as cardiovascular involvement (summary by Van Damme et al., 2017). For a general phenotypic description and a discussion of genetic heterogeneity of autosomal recessive cutis laxa, see ARCL1A (219100).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1385755">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1615526"><div><strong>Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1615526</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.">C4540367</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">SHRF is an autosomal recessive disorder characterized by short stature, brachydactyly, dysmorphic facial features, hearing loss, and visual impairment. Onset of the hearing and visual abnormalities, including retinitis pigmentosa, varies from birth to the second decade. Patients have mild intellectual disability and mild cerebellar atrophy with myelination defects on brain imaging (summary by Di Donato et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1615526">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1625009"><div><strong>Intellectual disability, autosomal dominant 51</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1625009</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.">C4540474</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1625009">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684324"><div><strong>Autosomal recessive spinocerebellar ataxia 20</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684324</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.">C5190595</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive spinocerebellar ataxia-20 is a neurodevelopmental disorder characterized by severely delayed psychomotor development with poor or absent speech, wide-based or absent gait, coarse facies, and cerebellar atrophy (summary by Thomas et al., 2014).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684324">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1674076"><div><strong>Shukla-Vernon syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1674076</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.">C5193146</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Shukla-Vernon syndrome (SHUVER) is an X-linked recessive neurodevelopmental disorder characterized by global developmental delay, variably impaired intellectual development, and behavioral abnormalities, including autism spectrum disorder and ADHD. Dysmorphic features are common and may include tall forehead, downslanting palpebral fissures, and tapering fingers. Some patients may have seizures and/or cerebellar atrophy on brain imaging. Carrier mothers may have mild manifestations, including learning disabilities (summary by Shukla et al., 2019).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1674076">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684805"><div><strong>Intellectual developmental disorder, autosomal recessive 72</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684805</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.">C5231452</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal recessive intellectual developmental disorder-72 (MRT72) is characterized by moderately to severely impaired intellectual development, microcephaly, and facial dysmorphism. Some patients may have seizures (Hu et al., 2019).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684805">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1803541"><div><strong>Stüve-Wiedemann syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1803541</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.">C5676888</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Stuve-Wiedemann syndrome is an autosomal recessive disorder characterized by bowing of the long bones and other skeletal anomalies, episodic hyperthermia, respiratory distress, and feeding difficulties usually resulting in early death (Dagoneau et al., 2004). See also 'classic' Schwartz-Jampel syndrome type 1 (SJS1; 255800), a phenotypically similar but genetically distinct disorder caused by mutation in the HSPG2 gene (142461) on chromosome 1p36. Genetic Heterogeneity of Stuve-Wiedemann Syndrome Stuve-Wiedemann syndrome-2 (STWS2; 619751) is caused by mutation in the IL6ST gene (600694) on chromosome 5q11.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1803541">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1855924"><div><strong>Megalencephaly-polydactyly syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1855924</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.">C5935591</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Megalencephaly-polydactyly syndrome (MPAPA) is an autosomal dominant disorder characterized by megalencephaly, ventriculomegaly, postaxial polydactyly, and, notably, neuroblastoma during infancy (summary by Nishio et al., 2023).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1855924">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1385755" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive cutis laxa type 2C</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684324" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive spinocerebellar ataxia 20</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_342675" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Gingival fibromatosis-hypertrichosis syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684805" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual developmental disorder, autosomal recessive 72</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_909304" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, autosomal dominant 39</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (12)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1625009" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, autosomal dominant 51</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_816016" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1855924" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Megalencephaly-polydactyly syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_220983" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nicolaides-Baraitser syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1615526" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1674076" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Shukla-Vernon syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1803541" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Stüve-Wiedemann syndrome 1</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/37804121">Consensus criteria for chronic rhinosinusitis disease control: an international Delphi Study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sedaghat AR,
|
||
Fokkens WJ,
|
||
Lund VJ,
|
||
Hellings PW,
|
||
Kern RC,
|
||
Reitsma S,
|
||
Toppila-Salmi S,
|
||
Bernal-Sprekelsen M,
|
||
Mullol J,
|
||
Gevaert P,
|
||
Teeling T,
|
||
Alobid I,
|
||
Anselmo-Lima WT,
|
||
Baroody FM,
|
||
Cervin A,
|
||
Cohen NA,
|
||
Constantinidis J,
|
||
De Gabory L,
|
||
Desrosiers M,
|
||
Harvey RJ,
|
||
Kalogjera L,
|
||
Knill A,
|
||
Landis BN,
|
||
Meco C,
|
||
Philpott CM,
|
||
Ryan D,
|
||
Schlosser RJ,
|
||
Senior BA,
|
||
Smith TL,
|
||
Tomazic PV,
|
||
Zhang L,
|
||
Hopkins C</span><br />
|
||
<span class="medgenPMjournal">Rhinology</span>
|
||
2023 Dec 1;61(6):519-530.
|
||
doi: 10.4193/Rhin23.335.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37804121" target="_blank">37804121</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34840009">Management of sinonasal cancers: Survey of UK practice and literature overview.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Iyizoba-Ebozue Z,
|
||
Fleming JC,
|
||
Prestwich RJD,
|
||
Thomson DJ</span><br />
|
||
<span class="medgenPMjournal">Eur J Surg Oncol</span>
|
||
2022 Jan;48(1):32-43.
|
||
Epub 2021 Nov 19
|
||
doi: 10.1016/j.ejso.2021.11.124.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34840009" target="_blank">34840009</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26097218">Dosing of sublingual immunotherapy for allergic rhinitis: evidence-based review with recommendations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leatherman BD,
|
||
Khalid A,
|
||
Lee S,
|
||
McMains K,
|
||
Peltier J,
|
||
Platt MP,
|
||
Stachler RJ,
|
||
Toskala E,
|
||
Tropper G,
|
||
Venkatraman G,
|
||
Lin SY</span><br />
|
||
<span class="medgenPMjournal">Int Forum Allergy Rhinol</span>
|
||
2015 Sep;5(9):773-83.
|
||
Epub 2015 Jun 11
|
||
doi: 10.1002/alr.21561.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26097218" target="_blank">26097218</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(wide%20nasal%20base)%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 (12)</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/30980075">Dorsal Roof Technique for Dorsum Preservation in Rhinoplasty.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Taş S</span><br />
|
||
<span class="medgenPMjournal">Aesthet Surg J</span>
|
||
2020 Feb 17;40(3):263-275.
|
||
doi: 10.1093/asj/sjz063.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30980075" target="_blank">30980075</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29409101">Surgical Tips for the Management of the Wide Nasal Base.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carniol ET,
|
||
Adamson PA</span><br />
|
||
<span class="medgenPMjournal">Facial Plast Surg</span>
|
||
2018 Feb;34(1):29-35.
|
||
Epub 2018 Feb 6
|
||
doi: 10.1055/s-0037-1621714.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29409101" target="_blank">29409101</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25595851">Evaluation of the nasal shape after orthognathic surgery.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dantas WR,
|
||
Silveira MM,
|
||
Vasconcelos BC,
|
||
Porto GG</span><br />
|
||
<span class="medgenPMjournal">Braz J Otorhinolaryngol</span>
|
||
2015 Jan-Feb;81(1):19-23.
|
||
Epub 2014 Aug 28
|
||
doi: 10.1016/j.bjorl.2014.08.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25595851" target="_blank">25595851</a><a href="/pmc/articles/PMC9452199" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21404164">Alar base reduction: the boomerang-shaped excision.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Foda HM</span><br />
|
||
<span class="medgenPMjournal">Facial Plast Surg</span>
|
||
2011 Apr;27(2):225-33.
|
||
Epub 2011 Mar 14
|
||
doi: 10.1055/s-0030-1271302.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21404164" target="_blank">21404164</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17224485">Nasal base narrowing: the combined alar base excision technique.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Foda HM</span><br />
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<span class="medgenPMjournal">Arch Facial Plast Surg</span>
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2007 Jan-Feb;9(1):30-4.
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<div class="nl"><a target="_blank" href="/pubmed/35970914">KBG syndrome: videoconferencing and use of artificial intelligence driven facial phenotyping in 25 new patients.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Guo L,
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<div class="nl"><a target="_blank" href="/pubmed/33817732">Case report of a novel phenotype in 18q deletion syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Bohîlţea RE,
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Cîrstoiu MM,
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Nedelea FM,
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Turcan N,
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<div class="nl"><a target="_blank" href="/pubmed/33234955">Systematic Surgical Approach to Alar Base Surgery in Rhinoplasty.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Rohrich RJ,
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Savetsky IL,
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Suszynski TM,
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Mohan R,
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Avashia YJ</span><br />
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<span class="medgenPMjournal">Plast Reconstr Surg</span>
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doi: 10.1097/PRS.0000000000007385.
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<span class="bold">PMID: </span><a href="/pubmed/33234955" target="_blank">33234955</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32688057">Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND).</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Vera G,
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Lesca G,
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Chatron N,
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Sabatier I,
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Duban-Bedu B,
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Colson C,
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Piton A,
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Durand B,
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Capri Y,
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Perrin L,
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Wiesener A,
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Zweier C,
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Maroofian R,
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Carroll CJ,
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Galehdari H,
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Mazaheri N,
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Callewaert B,
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Giulianno F,
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Zaafrane-Khachnaoui K,
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Haack T,
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Magg J,
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Rieß A,
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Horber V,
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Polli R,
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Turolla L,
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Murgia A,
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Frebourg T,
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<span class="medgenPMjournal">Eur J Med Genet</span>
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2020 Oct;63(10):104004.
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doi: 10.1016/j.ejmg.2020.104004.
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<span class="bold">PMID: </span><a href="/pubmed/32688057" target="_blank">32688057</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/22987502">Growth retardation, intellectual disability, facial anomalies, cataract, thoracic hypoplasia, and skeletal abnormalities: a novel phenotype.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Shah H,
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Bens S,
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Caliebe A,
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Graham JM Jr,
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Girisha KM</span><br />
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<span class="medgenPMjournal">Am J Med Genet A</span>
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2012 Nov;158A(11):2941-5.
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<span class="bold">PMID: </span><a href="/pubmed/22987502" target="_blank">22987502</a><a href="/pmc/articles/PMC3477260" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Wide%20nasal%20base%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 (7)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33234955">Systematic Surgical Approach to Alar Base Surgery in Rhinoplasty.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rohrich RJ,
|
||
Savetsky IL,
|
||
Suszynski TM,
|
||
Mohan R,
|
||
Avashia YJ</span><br />
|
||
<span class="medgenPMjournal">Plast Reconstr Surg</span>
|
||
2020 Dec;146(6):1259-1267.
|
||
doi: 10.1097/PRS.0000000000007385.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33234955" target="_blank">33234955</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30980075">Dorsal Roof Technique for Dorsum Preservation in Rhinoplasty.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Taş S</span><br />
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<span class="medgenPMjournal">Aesthet Surg J</span>
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2020 Feb 17;40(3):263-275.
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doi: 10.1093/asj/sjz063.
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<span class="bold">PMID: </span><a href="/pubmed/30980075" target="_blank">30980075</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29409101">Surgical Tips for the Management of the Wide Nasal Base.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carniol ET,
|
||
Adamson PA</span><br />
|
||
<span class="medgenPMjournal">Facial Plast Surg</span>
|
||
2018 Feb;34(1):29-35.
|
||
Epub 2018 Feb 6
|
||
doi: 10.1055/s-0037-1621714.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29409101" target="_blank">29409101</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26067559">Do the Size and Extension of the External Nasal Splint Have an Effect on the Osteotomy, Brow Lines, and Long-Term Results of Rhinoplasty: A Prospective Randomized Controlled Trial of 2 Methods.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Varedi P,
|
||
Bohluli B</span><br />
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<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
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||
2015 Sep;73(9):1843.e1-9.
|
||
Epub 2015 May 29
|
||
doi: 10.1016/j.joms.2015.05.027.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26067559" target="_blank">26067559</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Wide%20nasal%20base%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/29409101">Surgical Tips for the Management of the Wide Nasal Base.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carniol ET,
|
||
Adamson PA</span><br />
|
||
<span class="medgenPMjournal">Facial Plast Surg</span>
|
||
2018 Feb;34(1):29-35.
|
||
Epub 2018 Feb 6
|
||
doi: 10.1055/s-0037-1621714.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29409101" target="_blank">29409101</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26067559">Do the Size and Extension of the External Nasal Splint Have an Effect on the Osteotomy, Brow Lines, and Long-Term Results of Rhinoplasty: A Prospective Randomized Controlled Trial of 2 Methods.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Varedi P,
|
||
Bohluli B</span><br />
|
||
<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
|
||
2015 Sep;73(9):1843.e1-9.
|
||
Epub 2015 May 29
|
||
doi: 10.1016/j.joms.2015.05.027.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26067559" target="_blank">26067559</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23597951">A simplified approach to the external lateral nasal osteotomy: a technical note.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Varedi P,
|
||
Shirani G,
|
||
Bohluli B,
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||
Besharati R,
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||
Keyhan SO</span><br />
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<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
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||
2013 Aug;71(8):1435-8.
|
||
Epub 2013 Apr 15
|
||
doi: 10.1016/j.joms.2013.02.015.
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||
<span class="bold">PMID: </span><a href="/pubmed/23597951" target="_blank">23597951</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21493386">Nasal base narrowing: the alar flap advancement technique.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ismail AS</span><br />
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<span class="medgenPMjournal">Otolaryngol Head Neck Surg</span>
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2011 Jan;144(1):48-52.
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doi: 10.1177/0194599810390891.
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<span class="bold">PMID: </span><a href="/pubmed/21493386" target="_blank">21493386</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Wide%20nasal%20base%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 (4)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35675164">Total Aplasia of Paranasal Sinus Associated With a Syndromic Condition.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Doğan E,
|
||
Özgür E</span><br />
|
||
<span class="medgenPMjournal">Cleft Palate Craniofac J</span>
|
||
2023 May;60(5):616-620.
|
||
Epub 2022 Jun 8
|
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doi: 10.1177/10556656221074865.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35675164" target="_blank">35675164</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26067559">Do the Size and Extension of the External Nasal Splint Have an Effect on the Osteotomy, Brow Lines, and Long-Term Results of Rhinoplasty: A Prospective Randomized Controlled Trial of 2 Methods.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Varedi P,
|
||
Bohluli B</span><br />
|
||
<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
|
||
2015 Sep;73(9):1843.e1-9.
|
||
Epub 2015 May 29
|
||
doi: 10.1016/j.joms.2015.05.027.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26067559" target="_blank">26067559</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23597951">A simplified approach to the external lateral nasal osteotomy: a technical note.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Varedi P,
|
||
Shirani G,
|
||
Bohluli B,
|
||
Besharati R,
|
||
Keyhan SO</span><br />
|
||
<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
|
||
2013 Aug;71(8):1435-8.
|
||
Epub 2013 Apr 15
|
||
doi: 10.1016/j.joms.2013.02.015.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23597951" target="_blank">23597951</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22948628">Pentagonal hinge osteotomy for reduction of the wide nasal base of Asians.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lee YH,
|
||
Lee SH,
|
||
Hwang K</span><br />
|
||
<span class="medgenPMjournal">J Craniofac Surg</span>
|
||
2012 Sep;23(5):1442-3.
|
||
doi: 10.1097/SCS.0b013e31825e4b38.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22948628" target="_blank">22948628</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Wide%20nasal%20base%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 (4)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
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||
<div class="rightCol mgCol">
|
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<div class="portlet mgSection" id="ID_113">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul id="my-toc"></ul></div>
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<div class="portlet mgSection" id="ID_106">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Genetic_Testing_Registry">Genetic Testing Registry</h1><a sid="106" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C1849667%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (4)</a></li>
|
||
<li><a href="/gtr/tests?term=C1849667%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (4)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C1849667%5bDISCUI%5d" target="_blank">See all (4)</a></total></li>
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</ul></div>
|
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</div>
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<div class="portlet mgSection" id="ID_119">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Wide%20nasal%20base" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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</div>
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<div class="portlet mgSection" id="ID_121">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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