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<!--
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||
UID=98313
|
||
ConceptID=C0399352
|
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-->
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||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Anodontia</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>98313</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.">C0399352</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Total anodontia of permanent and deciduous teeth</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Developmental absence of tooth (234951001); Anodontia (26624006); Congenital absence of teeth (26624006); Anodontism (26624006); Congenital edentia (26624006); Agomphiasis (26624006); Agomphosis (26624006); Complete congenital absence of teeth (26624006)</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:0000674">HP:0000674</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0008797" target="_blank">MONDO:0008797</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=99797">ORPHA99797</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>
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||
<div class="portlet_content ln">The absence of all teeth from the normal series by a failure to develop. [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>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0399352[DISCUI]&test_type=Clinical" ref="ncbi_uid=98313">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 unavailable" title="ClinVar">V</span></span><span class="TLline">Anodontia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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/6447" ref="tree=MeSH" title="MedGen record for Abnormality of the mouth">Abnormality of the mouth</a></span><ul><li><span class="TLline"><a href="/medgen/1645271" ref="tree=MeSH" title="MedGen record for Abnormal oral morphology">Abnormal oral morphology</a></span><ul><li><span class="TLline"><a href="/medgen/871391" ref="tree=MeSH" title="MedGen record for Abnormal oral cavity morphology">Abnormal oral cavity morphology</a></span><ul><li><span class="TLline"><a href="/medgen/78084" ref="tree=MeSH" title="MedGen record for Abnormality of the dentition">Abnormality of the dentition</a></span><ul><li><span class="TLline"><a href="/medgen/11849" ref="tree=MeSH" title="MedGen record for Abnormal dental morphology">Abnormal dental morphology</a></span><ul><li><span class="matched_ds">Anodontia</span><ul><li><span class="TLline"><a href="/medgen/43794" ref="tree=MeSH" title="MedGen record for Hypodontia">Hypodontia</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</div>
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<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_83337"><div><strong>Woodhouse-Sakati syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>83337</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.">C0342286</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Virtually all individuals with Woodhouse-Sakati syndrome (WSS) have the endocrine findings of hypogonadism (evident at puberty) and progressive childhood-onset hair thinning that often progresses to alopecia totalis in adulthood. More than half of individuals have the neurologic findings of progressive extrapyramidal movements (dystonic spasms with dystonic posturing with dysarthria and dysphagia), moderate bilateral postlingual sensorineural hearing loss, and mild intellectual disability. To date, more than 40 families (including 33 with a molecularly confirmed diagnosis) with a total of 88 affected individuals have been reported in the literature.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/83337">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_96586"><div><strong>Cranioectodermal dysplasia 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>96586</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.">C0432235</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cranioectodermal dysplasia (CED) is a ciliopathy with skeletal involvement (narrow thorax, shortened proximal limbs, syndactyly, polydactyly, brachydactyly), ectodermal features (widely spaced hypoplastic teeth, hypodontia, sparse hair, skin laxity, abnormal nails), joint laxity, growth deficiency, and characteristic facial features (frontal bossing, low-set simple ears, high forehead, telecanthus, epicanthal folds, full cheeks, everted lower lip). Most affected children develop nephronophthisis that often leads to end-stage kidney disease in infancy or childhood, a major cause of morbidity and mortality. Hepatic fibrosis and retinal dystrophy are also observed. Dolichocephaly, often secondary to sagittal craniosynostosis, is a primary manifestation that distinguishes CED from most other ciliopathies. Brain malformations and developmental delay may also occur.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/96586">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_224851"><div><strong>Agenesis of permanent teeth</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>224851</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.">C1290511</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A congenital defect characterized by the absence of one or more permanent teeth, including oligodontia, hypodontia, and adontia of the of permanent teeth.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/224851">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_338272"><div><strong>Van der Woude syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>338272</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.">C1847604</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Van der Woude syndrome (VWS) is a dominantly inherited developmental disorder characterized by pits and/or sinuses of the lower lip, and cleft lip and/or cleft palate (CL/P, CP). It is the most common cleft syndrome. For a discussion of genetic heterogeneity of van der Woude syndrome, see VWS1 (119300).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/338272">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_410143"><div><strong>Tooth agenesis, selective, X-linked, 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>410143</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.">C1970757</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any tooth agenesis in which the cause of the disease is a mutation in the EDA gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/410143">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_444067"><div><strong>Cleft lip/palate-ectodermal dysplasia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>444067</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.">C2931488</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Zlotogora-Ogur syndrome is an ectodermal dysplasia syndrome with characteristics of hair, skin and teeth anomalies, facial dysmorphism with cleft lip and palate, cutaneous syndactyly and, in some cases, intellectual disability.The prevalence is unknown but to date, less than 50 cases have been described in the literature. Caused by mutations in the gene PVRL1 (11q23-q24) which encodes nectin-1, the principal receptor used by alpha-herpesviruses to mediate entry into human cells. Transmission is autosomal recessive.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/444067">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_477139"><div><strong>Multiple congenital anomalies-hypotonia-seizures syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>477139</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.">C3275508</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Multiple congenital anomalies-hypotonia-seizures syndrome-2 (MCAHS2) is an X-linked recessive neurodevelopmental disorder characterized by dysmorphic features, neonatal hypotonia, early-onset myoclonic seizures, and variable congenital anomalies involving the central nervous, cardiac, and urinary systems. Some affected individuals die in infancy (summary by Johnston et al., 2012). The phenotype shows clinical variability with regard to severity and extraneurologic features. However, most patients present in infancy with early-onset epileptic encephalopathy associated with developmental arrest and subsequent severe neurologic disability; these features are consistent with a form of developmental and epileptic encephalopathy (DEE) (summary by Belet et al., 2014, Kato et al., 2014). The disorder is caused by a defect in glycosylphosphatidylinositol (GPI) biosynthesis. For a discussion of genetic heterogeneity of MCAHS, see MCAHS1 (614080). For a discussion of nomenclature and genetic heterogeneity of DEE, see 308350. For a discussion of genetic heterogeneity of GPI biosynthesis defects, see GPIBD1 (610293).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/477139">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_854356"><div><strong>Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>854356</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.">C3887494</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypohidrotic ectodermal dysplasia (HED) is characterized by hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth). The cardinal features of classic HED become obvious during childhood. The scalp hair is thin, lightly pigmented, and slow growing. Sweating, although present, is greatly deficient, leading to episodes of hyperthermia until the affected individual or family acquires experience with environmental modifications to control temperature. Only a few abnormally formed teeth erupt, at a later-than-average age. Physical growth and psychomotor development are otherwise within normal limits. Mild HED is characterized by mild manifestations of any or all the characteristic features.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/854356">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_854747"><div><strong>Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>854747</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.">C3888065</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypohidrotic ectodermal dysplasia (HED) is characterized by hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth). The cardinal features of classic HED become obvious during childhood. The scalp hair is thin, lightly pigmented, and slow growing. Sweating, although present, is greatly deficient, leading to episodes of hyperthermia until the affected individual or family acquires experience with environmental modifications to control temperature. Only a few abnormally formed teeth erupt, at a later-than-average age. Physical growth and psychomotor development are otherwise within normal limits. Mild HED is characterized by mild manifestations of any or all the characteristic features.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/854747">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_224851" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Agenesis of permanent teeth</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_444067" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cleft lip/palate-ectodermal dysplasia syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_96586" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cranioectodermal dysplasia 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_854747" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_854356" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (9)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_477139" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Multiple congenital anomalies-hypotonia-seizures syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_410143" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Tooth agenesis, selective, X-linked, 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_338272" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Van der Woude syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_83337" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Woodhouse-Sakati syndrome</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/36922297">Removable prosthetic management for tooth agenesis in the pediatric population: A systematic review of case reports and case series.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Varghese AA,
|
||
Xavier AM,
|
||
Ramanarayanan V</span><br />
|
||
<span class="medgenPMjournal">J Prosthet Dent</span>
|
||
2024 Dec;132(6):1250.e1-1250.e8.
|
||
Epub 2023 Mar 13
|
||
doi: 10.1016/j.prosdent.2023.02.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36922297" target="_blank">36922297</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37355575">A comparative retrospective study on the prevalence and therapeutic treatment of dental agenesis between healthy children and children with systemic disease or congenital malformation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nadolinski M,
|
||
Schlenz MA,
|
||
Rahman A,
|
||
Krämer N,
|
||
Schulz-Weidner N</span><br />
|
||
<span class="medgenPMjournal">BMC Pediatr</span>
|
||
2023 Jun 24;23(1):322.
|
||
doi: 10.1186/s12887-023-04138-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37355575" target="_blank">37355575</a><a href="/pmc/articles/PMC10290303" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23406509">Treatment for agenesis of maxillary lateral incisors: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Andrade DC,
|
||
Loureiro CA,
|
||
Araújo VE,
|
||
Riera R,
|
||
Atallah AN</span><br />
|
||
<span class="medgenPMjournal">Orthod Craniofac Res</span>
|
||
2013 Aug;16(3):129-36.
|
||
Epub 2013 Feb 14
|
||
doi: 10.1111/ocr.12015.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23406509" target="_blank">23406509</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22anodontia%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 (6)</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/29364747">Rare and Common Variants Conferring Risk of Tooth Agenesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jonsson L,
|
||
Magnusson TE,
|
||
Thordarson A,
|
||
Jonsson T,
|
||
Geller F,
|
||
Feenstra B,
|
||
Melbye M,
|
||
Nohr EA,
|
||
Vucic S,
|
||
Dhamo B,
|
||
Rivadeneira F,
|
||
Ongkosuwito EM,
|
||
Wolvius EB,
|
||
Leslie EJ,
|
||
Marazita ML,
|
||
Howe BJ,
|
||
Moreno Uribe LM,
|
||
Alonso I,
|
||
Santos M,
|
||
Pinho T,
|
||
Jonsson R,
|
||
Audolfsson G,
|
||
Gudmundsson L,
|
||
Nawaz MS,
|
||
Olafsson S,
|
||
Gustafsson O,
|
||
Ingason A,
|
||
Unnsteinsdottir U,
|
||
Bjornsdottir G,
|
||
Walters GB,
|
||
Zervas M,
|
||
Oddsson A,
|
||
Gudbjartsson DF,
|
||
Steinberg S,
|
||
Stefansson H,
|
||
Stefansson K</span><br />
|
||
<span class="medgenPMjournal">J Dent Res</span>
|
||
2018 May;97(5):515-522.
|
||
Epub 2018 Jan 24
|
||
doi: 10.1177/0022034517750109.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29364747" target="_blank">29364747</a><a href="/pmc/articles/PMC5958369" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28933802">Investigation of prevalence of dental anomalies by using digital panoramic radiographs.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bilge NH,
|
||
Yeşiltepe S,
|
||
Törenek Ağırman K,
|
||
Çağlayan F,
|
||
Bilge OM</span><br />
|
||
<span class="medgenPMjournal">Folia Morphol (Warsz)</span>
|
||
2018;77(2):323-328.
|
||
Epub 2017 Sep 21
|
||
doi: 10.5603/FM.a2017.0087.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28933802" target="_blank">28933802</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29027749">Permanent tooth agenesis in individuals with non-syndromic Robin sequence: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Antonarakis GS,
|
||
Palaska PK,
|
||
Suri S</span><br />
|
||
<span class="medgenPMjournal">Orthod Craniofac Res</span>
|
||
2017 Nov;20(4):216-226.
|
||
Epub 2017 Oct 13
|
||
doi: 10.1111/ocr.12204.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29027749" target="_blank">29027749</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24010518">Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vasconcelos Carvalho M,
|
||
Romero Souto de Sousa J,
|
||
Paiva Correa de Melo F,
|
||
Fonseca Faro T,
|
||
Nunes Santos AC,
|
||
Carvalho S,
|
||
Veras Sobral AP</span><br />
|
||
<span class="medgenPMjournal">Dermatol Online J</span>
|
||
2013 Jul 14;19(7):18985.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24010518" target="_blank">24010518</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2192761">Prevalence of hypodontia and developmental malformation of permanent teeth in Saudi Arabian schoolchildren.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">al-Emran S</span><br />
|
||
<span class="medgenPMjournal">Br J Orthod</span>
|
||
1990 May;17(2):115-8.
|
||
doi: 10.1179/bjo.17.2.115.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2192761" target="_blank">2192761</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Anodontia%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 (984)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35674572">Agenesis of maxillary lateral incisors: diagnosis and treatment options.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Schroeder DK,
|
||
Schroeder MA,
|
||
Vasconcelos V</span><br />
|
||
<span class="medgenPMjournal">Dental Press J Orthod</span>
|
||
2022;27(1):e22spe1.
|
||
Epub 2022 Jun 6
|
||
doi: 10.1590/2177-6709.27.1.e22spe1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35674572" target="_blank">35674572</a><a href="/pmc/articles/PMC9172892" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27381090">MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liang J,
|
||
Von den Hoff J,
|
||
Lange J,
|
||
Ren Y,
|
||
Bian Z,
|
||
Carels CE</span><br />
|
||
<span class="medgenPMjournal">Eur J Hum Genet</span>
|
||
2016 Dec;24(12):1663-1670.
|
||
Epub 2016 Jul 6
|
||
doi: 10.1038/ejhg.2016.78.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27381090" target="_blank">27381090</a><a href="/pmc/articles/PMC5117928" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21273721">Familial hypophosphatemic rickets.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sattur A,
|
||
Naikmasur VG,
|
||
Shrivastava R,
|
||
Babshet M</span><br />
|
||
<span class="medgenPMjournal">J Indian Soc Pedod Prev Dent</span>
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2010 Oct-Dec;28(4):302-6.
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<div class="nl"><a target="_blank" href="/pubmed/20139583">Progeria.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mohamed Riyaz SS,
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2009 Oct-Dec;20(4):508-10.
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<span class="bold">PMID: </span><a href="/pubmed/20139583" target="_blank">20139583</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/9603237">Neuro-osteology.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Kjaer I</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/9603237" target="_blank">9603237</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Anodontia%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 (685)</a></div><h3 class="subhead">Therapy</h3>
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<div class="nl"><a target="_blank" href="/pubmed/39389160">Development of a new antibody drug to treat congenital tooth agenesis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Takahashi K,
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Kiso H,
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Mihara E,
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Takagi J,
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Tokita Y,
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<span class="bold">PMID: </span><a href="/pubmed/39389160" target="_blank">39389160</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/36253866">Orthodontic and dentofacial orthopedic treatments in patients with ectodermal dysplasia: a systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Cerezo-Cayuelas M,
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Pérez-Silva A,
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Serna-Muñoz C,
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Vicente A,
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Martínez-Beneyto Y,
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Cabello-Malagón I,
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Ortiz-Ruiz AJ</span><br />
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<div class="nl"><a target="_blank" href="/pubmed/2192761">Prevalence of hypodontia and developmental malformation of permanent teeth in Saudi Arabian schoolchildren.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/359378">The median diastema.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Becker A</span><br />
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<span class="medgenPMjournal">Dent Clin North Am</span>
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<span class="bold">PMID: </span><a href="/pubmed/359378" target="_blank">359378</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/4159144">Thalidomide.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Speirs AL</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/4159144" target="_blank">4159144</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Anodontia%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 (164)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28401166">Hypodontia: An Update on Its Etiology, Classification, and Clinical Management.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Al-Ani AH,
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Antoun JS,
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Thomson WM,
|
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Merriman TR,
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Farella M</span><br />
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<span class="medgenPMjournal">Biomed Res Int</span>
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2017;2017:9378325.
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Epub 2017 Mar 19
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doi: 10.1155/2017/9378325.
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<span class="bold">PMID: </span><a href="/pubmed/28401166" target="_blank">28401166</a><a href="/pmc/articles/PMC5376450" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26600092">Hypodontia, a prospective predictive marker for tumor?</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Yin W,
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Bian Z</span><br />
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<span class="medgenPMjournal">Oral Dis</span>
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2016 May;22(4):265-73.
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Epub 2016 Jan 13
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doi: 10.1111/odi.12400.
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<span class="bold">PMID: </span><a href="/pubmed/26600092" target="_blank">26600092</a></div>
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||
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<div class="nl"><a target="_blank" href="/pubmed/21417113">Tooth autotransplantation as a treatment option: a review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Park JH,
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Tai K,
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Hayashi D</span><br />
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<span class="medgenPMjournal">J Clin Pediatr Dent</span>
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2010 Winter;35(2):129-35.
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doi: 10.17796/jcpd.35.2.97816254u2140x88.
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<span class="bold">PMID: </span><a href="/pubmed/21417113" target="_blank">21417113</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/15934680">Managing congenitally missing lateral incisors. Part I: Canine substitution.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kokich VO Jr,
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Kinzer GA</span><br />
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<span class="medgenPMjournal">J Esthet Restor Dent</span>
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2005;17(1):5-10.
|
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doi: 10.1111/j.1708-8240.2005.tb00076.x.
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<span class="bold">PMID: </span><a href="/pubmed/15934680" target="_blank">15934680</a></div>
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||
|
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<div class="nl"><a target="_blank" href="/pubmed/9603237">Neuro-osteology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kjaer I</span><br />
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<span class="medgenPMjournal">Crit Rev Oral Biol Med</span>
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1998;9(2):224-44.
|
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doi: 10.1177/10454411980090020501.
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<span class="bold">PMID: </span><a href="/pubmed/9603237" target="_blank">9603237</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Anodontia%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 (456)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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||
<div class="nl"><a target="_blank" href="/pubmed/36378475">Rethinking the Genetic Etiology of Nonsyndromic Tooth Agenesis.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Letra A</span><br />
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<span class="medgenPMjournal">Curr Osteoporos Rep</span>
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2022 Dec;20(6):389-397.
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Epub 2022 Nov 15
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doi: 10.1007/s11914-022-00761-8.
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<span class="bold">PMID: </span><a href="/pubmed/36378475" target="_blank">36378475</a><a href="/pmc/articles/PMC10752440" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28401166">Hypodontia: An Update on Its Etiology, Classification, and Clinical Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Al-Ani AH,
|
||
Antoun JS,
|
||
Thomson WM,
|
||
Merriman TR,
|
||
Farella M</span><br />
|
||
<span class="medgenPMjournal">Biomed Res Int</span>
|
||
2017;2017:9378325.
|
||
Epub 2017 Mar 19
|
||
doi: 10.1155/2017/9378325.
|
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<span class="bold">PMID: </span><a href="/pubmed/28401166" target="_blank">28401166</a><a href="/pmc/articles/PMC5376450" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26600092">Hypodontia, a prospective predictive marker for tumor?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yin W,
|
||
Bian Z</span><br />
|
||
<span class="medgenPMjournal">Oral Dis</span>
|
||
2016 May;22(4):265-73.
|
||
Epub 2016 Jan 13
|
||
doi: 10.1111/odi.12400.
|
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<span class="bold">PMID: </span><a href="/pubmed/26600092" target="_blank">26600092</a></div>
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||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18186725">Mouse models of tooth abnormalities.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Fleischmannova J,
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Matalova E,
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Tucker AS,
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Sharpe PT</span><br />
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<span class="medgenPMjournal">Eur J Oral Sci</span>
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2008 Feb;116(1):1-10.
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doi: 10.1111/j.1600-0722.2007.00504.x.
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<span class="bold">PMID: </span><a href="/pubmed/18186725" target="_blank">18186725</a></div>
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||
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||
<div class="nl"><a target="_blank" href="/pubmed/15934680">Managing congenitally missing lateral incisors. Part I: Canine substitution.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kokich VO Jr,
|
||
Kinzer GA</span><br />
|
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<span class="medgenPMjournal">J Esthet Restor Dent</span>
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2005;17(1):5-10.
|
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doi: 10.1111/j.1708-8240.2005.tb00076.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15934680" target="_blank">15934680</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Anodontia%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 (581)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/39578995">Does Current Evidence Support the Discussion Around the Guidance Theory? A Systematic Review and Meta-Analysis on the Association Between Maxillary Lateral Incisor Agenesis and Displacement or Impaction of the Permanent Canine.</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Papageorgiou SN,
|
||
Seehra J,
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||
Cobourne MT,
|
||
Kanavakis G</span><br />
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||
<span class="medgenPMjournal">Orthod Craniofac Res</span>
|
||
2025 Apr;28(2):312-323.
|
||
Epub 2024 Nov 23
|
||
doi: 10.1111/ocr.12878.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39578995" target="_blank">39578995</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36253866">Orthodontic and dentofacial orthopedic treatments in patients with ectodermal dysplasia: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cerezo-Cayuelas M,
|
||
Pérez-Silva A,
|
||
Serna-Muñoz C,
|
||
Vicente A,
|
||
Martínez-Beneyto Y,
|
||
Cabello-Malagón I,
|
||
Ortiz-Ruiz AJ</span><br />
|
||
<span class="medgenPMjournal">Orphanet J Rare Dis</span>
|
||
2022 Oct 17;17(1):376.
|
||
doi: 10.1186/s13023-022-02533-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36253866" target="_blank">36253866</a><a href="/pmc/articles/PMC9575248" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33030085">Association between Dental Anomalies and Orofacial Clefts: A Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marzouk T,
|
||
Alves IL,
|
||
Wong CL,
|
||
DeLucia L,
|
||
McKinney CM,
|
||
Pendleton C,
|
||
Howe BJ,
|
||
Marazita ML,
|
||
Peter TK,
|
||
Kopycka-Kedzierawski DT,
|
||
Morrison CS,
|
||
Malmstrom H,
|
||
Wang H,
|
||
Shope ET</span><br />
|
||
<span class="medgenPMjournal">JDR Clin Trans Res</span>
|
||
2021 Oct;6(4):368-381.
|
||
Epub 2020 Oct 8
|
||
doi: 10.1177/2380084420964795.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33030085" target="_blank">33030085</a><a href="/pmc/articles/PMC8447105" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29461745">The Current Evidence on Retaining or Prosthodontically Replacing Retained Deciduous Teeth in the Adult Hypodontia Patient: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Laverty DP,
|
||
Fairbrother K,
|
||
Addison O</span><br />
|
||
<span class="medgenPMjournal">Eur J Prosthodont Restor Dent</span>
|
||
2018 Mar 1;26(1):2-15.
|
||
doi: 10.1922/EJPRD_01721Laverty14.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29461745" target="_blank">29461745</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29027749">Permanent tooth agenesis in individuals with non-syndromic Robin sequence: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Antonarakis GS,
|
||
Palaska PK,
|
||
Suri S</span><br />
|
||
<span class="medgenPMjournal">Orthod Craniofac Res</span>
|
||
2017 Nov;20(4):216-226.
|
||
Epub 2017 Oct 13
|
||
doi: 10.1111/ocr.12204.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29027749" target="_blank">29027749</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Anodontia%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 (37)</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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|
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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 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=C0399352%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (4)</a></li>
|
||
<li><a href="/gtr/tests?term=C0399352%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=C0399352%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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|
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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="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=99797" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Anodontia" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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|
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|
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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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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22anodontia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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