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<meta name="keywords" content="C0266063, deep bite, deep overbite, disease or syndrome, excessive overbite, increased overbite, increased overlap of upper and lower incisors, overbite, scissors bite, supraocclusion, 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="Maxillary teeth cover the mandibular teeth when biting to an increased degree. The feature is defined as a vertical overlap of the maxillary incisors over the mandibular incisors that exceeds 2 mm." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Increased overbite (Concept Id: C0266063)
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<!--
UID=539656
ConceptID=C0266063
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Increased overbite</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>539656</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)&#10;Click for more information."><span class="highlight" style="background-color:">C0266063</span></a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
<td>Overbite</td></tr>
<tr><td><span class="bold">SNOMED CT: </span></td>
<td>Deep overbite (60476005); Increased overbite (60476005); Excessive overbite (60476005)</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:0011094">HP:0011094</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>
<div class="portlet mgSection" id="ID_100">
<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">Maxillary teeth cover the mandibular teeth when biting to an increased degree. The feature is defined as a vertical overlap of the maxillary incisors over the mandibular incisors that exceeds 2 mm. [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 mgSection" id="ID_118">
<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=C0266063[DISCUI]&amp;test_type=Clinical&amp;redirect=true" ref="ncbi_uid=539656">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&amp;from_uid=539656" ref="ncbi_uid=539656">V</a></span></span><span class="TLline">Increased overbite</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/377692" ref="tree=MeSH" title="MedGen record for Tooth malposition">Tooth malposition</a></span><ul><li><span class="matched_ds">Increased overbite</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_332392"><div><strong>Isolated cleft palate</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>332392</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)&#10;Click for more information.">C1837218</a></dd><dt><span class="dotprefix"></span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
<div class="spaceAbove">Cleft palate as an isolated malformation behaves as an entity distinct from cleft lip with or without cleft palate (see 119530).&#13; Dominantly inherited cleft soft palate in 4 generations has been reported (Jenkins and Stady, 1980); see 119570.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/332392">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_350085"><div><strong>Spinocerebellar ataxia type 29</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>350085</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)&#10;Click for more information.">C1861732</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Spinocerebellar ataxia-29 (SCA29) is an autosomal dominant neurologic disorder characterized by onset in infancy of delayed motor development and mild cognitive delay. Affected individuals develop a very slowly progressive or nonprogressive gait and limb ataxia associated with cerebellar atrophy on brain imaging. Additional variable features include nystagmus, dysarthria, and tremor (summary by Huang et al., 2012).&#13; For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/350085">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_462291"><div><strong>Rubinstein-Taybi syndrome due to EP300 haploinsufficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>462291</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)&#10;Click for more information.">C3150941</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Rubinstein-Taybi syndrome (RSTS) is characterized by distinctive facial features, broad and often angulated thumbs and halluces, short stature, and moderate-to-severe intellectual disability. Characteristic craniofacial features include downslanted palpebral fissures, low-hanging columella, high palate, grimacing smile, and talon cusps. Prenatal growth is often normal, then height, weight, and head circumference percentiles rapidly drop in the first few months of life. Short stature is typical in adulthood. Obesity may develop in childhood or adolescence. Average IQ ranges between 35 and 50; however, developmental outcome varies considerably. Some individuals with EP300-related RSTS have normal intellect. Additional features include ocular abnormalities, hearing loss, respiratory difficulties, congenital heart defects, renal abnormalities, cryptorchidism, feeding problems, recurrent infections, and severe constipation.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/462291">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_934597"><div><strong>Amelogenesis imperfecta, type 1J</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934597</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)&#10;Click for more information.">C4310630</a></dd><dt><span class="dotprefix"></span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
<div class="spaceAbove">Amelogenesis imperfecta is an inherited defect of dental enamel formation that shows both clinical and genetic heterogeneity. In the hypoplastic type of AI, the enamel is of normal hardness but does not develop to normal thickness. The thinness of the enamel makes the teeth appear small. Radiographically, enamel contrasts normally from dentin. The surface of the enamel can vary, showing smooth, rough, pitted, or local forms (Witkop, 1988).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/934597">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_934738"><div><strong>Intellectual disability, autosomal dominant 43</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934738</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)&#10;Click for more information.">C4310771</a></dd><dt><span class="dotprefix"></span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
<div class="spaceAbove">HIVEP2-related intellectual disability is a neurological disorder characterized by moderate to severe developmental delay and intellectual disability and mild physical abnormalities (dysmorphic features). Early symptoms of the condition include weak muscle tone (hypotonia) and delayed development of motor skills, such as sitting, standing, and walking. After learning to walk, many affected individuals continue to have difficulty with this activity; their walking style (gait) is often unbalanced and wide-based. Speech is also delayed, and some people with this condition never learn to talk. Most people with HIVEP2-related intellectual disability also have unusual physical features, such as widely spaced eyes (hypertelorism), a broad nasal bridge, or fingers with tapered ends, although there is no characteristic pattern of such features among affected individuals. Many people with the condition exhibit neurodevelopmental disorders, such as hyperactivity, attention deficit disorder, aggression, anxiety, and autism spectrum disorder, which is a group of developmental disorders characterized by impaired communication and social interaction.\n\nOther features of HIVEP2-related intellectual disability include mild abnormalities in the structure of the brain and an abnormally small brain and head size (microcephaly). Less common health problems include seizures; recurrent ear infections; and eye disorders, such as eyes that do not look in the same direction (strabismus), "lazy eye" (amblyopia), and farsightedness (hyperopia). Some people with HIVEP2-related intellectual disability have gastrointestinal problems, which can include backflow of acidic stomach contents into the esophagus (gastroesophageal reflux) and constipation.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/934738">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1632634"><div><strong>Branchiootorenal syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1632634</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)&#10;Click for more information.">C4551702</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Branchiootorenal spectrum disorder (BORSD) is characterized by malformations of the outer, middle, and inner ear associated with conductive, sensorineural, or mixed hearing impairment, branchial fistulae and cysts, and renal malformations ranging from mild renal hypoplasia to bilateral renal agenesis. Some individuals progress to end-stage renal disease (ESRD) later in life. Extreme variability can be observed in the presence, severity, and type of branchial arch, otologic, audiologic, and renal abnormality from right side to left side in an affected individual and also among individuals in the same family.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1632634">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1673448"><div><strong>Intellectual developmental disorder, autosomal recessive 71</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1673448</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)&#10;Click for more information.">C5193133</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1673448">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1684686"><div><strong>Catifa syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684686</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)&#10;Click for more information.">C5231492</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">CATIFA syndrome is characterized by global developmental delay and impaired intellectual development ranging from mild to severe, with most patients exhibiting attention-deficit hyperactivity disorder (ADHD). Patients show an elongated face with long philtrum and small ears. Ocular anomalies include congenital cataracts, strabismus, and amblyopia, which may be associated with reduced vision; other anomalies include cleft lip and/or palate and misaligned teeth with extensive caries (Unlu et al., 2020).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1684686">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1800921"><div><strong>Carey-Fineman-Ziter syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1800921</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)&#10;Click for more information.">C5677012</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Carey-Fineman-Ziter syndrome-2 (CFZS2) is an autosomal recessive neuromuscular disorder characterized by motor developmental delay, facial weakness, hypotonia, growth restriction, feeding difficulties, and velopharyngeal insufficiency. Additional variable features include hearing loss, scoliosis, joint contractures, cleft palate, hypoglossia, and abnormalities on neuroimaging studies (summary by Rahman et al., 2024).&#13; For a discussion of genetic heterogeneity of Carey-Fineman-Ziter syndrome, see CFZS1 (254940).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1800921">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1841272"><div><strong>Intellectual developmental disorder, autosomal dominant 73</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1841272</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)&#10;Click for more information.">C5830636</a></dd><dt><span class="dotprefix"></span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
<div class="spaceAbove">Autosomal dominant intellectual developmental disorder-73 (MRD73) is a highly variable neurodevelopmental disorder characterized by impaired intellectual development that ranges from mild to severe, speech delay, behavioral abnormalities, and nonspecific dysmorphic facial features (Janssen et al., 2022).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1841272">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1863661"><div><strong>Neuroocular syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1863661</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)&#10;Click for more information.">C5925133</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Neuroocular syndrome-1 (NOC1) encompasses a broad spectrum of overlapping anomalies, with developmental delay or impaired intellectual development as a consistent finding. Eye abnormalities show marked variability in the type and severity of defects, and include anophthalmia, microphthalmia, and coloboma. Other common systemic features include congenital heart and kidney defects, hypotonia, failure to thrive, and microcephaly (summary by Chowdhury et al., 2021).&#13; Genetic Heterogeneity of Neuroocular Syndrome&#13; See also NOC2 (168885), caused by mutation in the DAGLA gene (614015) on chromosome 11q12.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1863661">Condition Record</a></div></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934597" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Amelogenesis imperfecta, type 1J</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1632634" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Branchiootorenal syndrome 1</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1800921" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Carey-Fineman-Ziter syndrome 2</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684686" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Catifa syndrome</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1841272" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual developmental disorder, autosomal dominant 73</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (11)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1673448" 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 71</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934738" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, autosomal dominant 43</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_332392" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Isolated cleft palate</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1863661" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neuroocular syndrome 1</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_462291" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Rubinstein-Taybi syndrome due to EP300 haploinsufficiency</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_350085" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia type 29</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/30075925">Factors affecting treatment decisions for Class I malocclusions.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Ali B,
Shaikh A,
Fida M</span><br />
<span class="medgenPMjournal">Am J Orthod Dentofacial Orthop</span>
2018 Aug;154(2):234-237.
doi: 10.1016/j.ajodo.2017.11.035.
<span class="bold">PMID: </span><a href="/pubmed/30075925" target="_blank">30075925</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29390172">Orthodontic treatment for deep bite and retroclined upper front teeth in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Millett DT,
Cunningham SJ,
O'Brien KD,
Benson PE,
de Oliveira CM</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Feb 1;2(2):CD005972.
doi: 10.1002/14651858.CD005972.pub4.
<span class="bold">PMID: </span><a href="/pubmed/29390172" target="_blank">29390172</a><a href="/pmc/articles/PMC6491166" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28968484">Orthodontic treatment for deep bite and retroclined upper front teeth in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Millett DT,
Cunningham SJ,
O'Brien KD,
Benson PE,
de Oliveira CM</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2017 Oct 2;10(10):CD005972.
doi: 10.1002/14651858.CD005972.pub3.
<span class="bold">PMID: </span><a href="/pubmed/28968484" target="_blank">28968484</a><a href="/pmc/articles/PMC6485795" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22increased%20overbite%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 (17)</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/29390172">Orthodontic treatment for deep bite and retroclined upper front teeth in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Millett DT,
Cunningham SJ,
O'Brien KD,
Benson PE,
de Oliveira CM</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Feb 1;2(2):CD005972.
doi: 10.1002/14651858.CD005972.pub4.
<span class="bold">PMID: </span><a href="/pubmed/29390172" target="_blank">29390172</a><a href="/pmc/articles/PMC6491166" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28968484">Orthodontic treatment for deep bite and retroclined upper front teeth in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Millett DT,
Cunningham SJ,
O'Brien KD,
Benson PE,
de Oliveira CM</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2017 Oct 2;10(10):CD005972.
doi: 10.1002/14651858.CD005972.pub3.
<span class="bold">PMID: </span><a href="/pubmed/28968484" target="_blank">28968484</a><a href="/pmc/articles/PMC6485795" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26892218">Caries Experience in Individuals with Moebius Syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Castro T,
Ortega AO,
Mussi MC,
Braga MM,
Gallottini M</span><br />
<span class="medgenPMjournal">Pediatr Dent</span>
2016 Jan-Feb;38(1):68-71.
<span class="bold">PMID: </span><a href="/pubmed/26892218" target="_blank">26892218</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26349294">Extreme Dental Compensation in an Adult Skeletal Class III Malocclusion: 3-Year Follow-up of a Successfully Compromised Treatment.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Estelita S,
Janson G,
Chiqueto K</span><br />
<span class="medgenPMjournal">Int J Orthod Milwaukee</span>
2015 Summer;26(2):69-76.
<span class="bold">PMID: </span><a href="/pubmed/26349294" target="_blank">26349294</a></div>
<div class="nl"><a target="_blank" href="/pubmed/7676364">Sickle cell anemia: a review of the dental concerns and a retrospective study of dental and bony changes.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Taylor LB,
Nowak AJ,
Giller RH,
Casamassimo PS</span><br />
<span class="medgenPMjournal">Spec Care Dentist</span>
1995 Jan-Feb;15(1):38-42.
doi: 10.1111/j.1754-4505.1995.tb00469.x.
<span class="bold">PMID: </span><a href="/pubmed/7676364" target="_blank">7676364</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Increased%20overbite%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 (40)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/30567451">Prevalence of craniomandibular disorders in orthodontic pediatric population and possible interactions with anxiety and stress.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Romani V,
Di Giorgio R,
Castellano M,
Barbato E,
Galluccio G</span><br />
<span class="medgenPMjournal">Eur J Paediatr Dent</span>
2018 Dec;19(4):317-323.
doi: 10.23804/ejpd.2018.19.04.13.
<span class="bold">PMID: </span><a href="/pubmed/30567451" target="_blank">30567451</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26892218">Caries Experience in Individuals with Moebius Syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Castro T,
Ortega AO,
Mussi MC,
Braga MM,
Gallottini M</span><br />
<span class="medgenPMjournal">Pediatr Dent</span>
2016 Jan-Feb;38(1):68-71.
<span class="bold">PMID: </span><a href="/pubmed/26892218" target="_blank">26892218</a></div>
<div class="nl"><a target="_blank" href="/pubmed/21070327">Do malocclusion and Helkimo Index ≥ 5 correlate with body posture?</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Perillo L,
Femminella B,
Farronato D,
Baccetti T,
Contardo L,
Perinetti G</span><br />
<span class="medgenPMjournal">J Oral Rehabil</span>
2011 Apr;38(4):242-52.
doi: 10.1111/j.1365-2842.2010.02156.x.
<span class="bold">PMID: </span><a href="/pubmed/21070327" target="_blank">21070327</a></div>
<div class="nl"><a target="_blank" href="/pubmed/17095742">Orthodontic treatment need in French schoolchildren: an epidemiological study using the Index of Orthodontic Treatment Need.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Souames M,
Bassigny F,
Zenati N,
Riordan PJ,
Boy-Lefevre ML</span><br />
<span class="medgenPMjournal">Eur J Orthod</span>
2006 Dec;28(6):605-9.
Epub 2006 Nov 9
doi: 10.1093/ejo/cjl045.
<span class="bold">PMID: </span><a href="/pubmed/17095742" target="_blank">17095742</a></div>
<div class="nl"><a target="_blank" href="/pubmed/12166910">Selection of criteria for assessment of occlusal acceptability.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Svedström-Oristo AL,
Pietilä T,
Pietilä I,
Helenius H,
Peutzfeldt P,
Varrela J</span><br />
<span class="medgenPMjournal">Acta Odontol Scand</span>
2002 Jun;60(3):160-6.
doi: 10.1080/000163502753740188.
<span class="bold">PMID: </span><a href="/pubmed/12166910" target="_blank">12166910</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Increased%20overbite%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/35059463">Bracket Failure in Orthodontic Patients: The Incidence and the Influence of Different Factors.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Khan H,
Mheissen S,
Iqbal A,
Jafri AR,
Alam MK</span><br />
<span class="medgenPMjournal">Biomed Res Int</span>
2022;2022:5128870.
Epub 2022 Jan 11
doi: 10.1155/2022/5128870.
<span class="bold">PMID: </span><a href="/pubmed/35059463" target="_blank">35059463</a><a href="/pmc/articles/PMC8766193" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33723104">Cephalometric evaluation of hyoid bone position in subjects with different vertical dental patterns.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Soyoye OA,
Otuyemi OD,
Newman-Nartey M</span><br />
<span class="medgenPMjournal">Niger J Clin Pract</span>
2021 Mar;24(3):321-328.
doi: 10.4103/njcp.njcp_430_20.
<span class="bold">PMID: </span><a href="/pubmed/33723104" target="_blank">33723104</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30075925">Factors affecting treatment decisions for Class I malocclusions.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Ali B,
Shaikh A,
Fida M</span><br />
<span class="medgenPMjournal">Am J Orthod Dentofacial Orthop</span>
2018 Aug;154(2):234-237.
doi: 10.1016/j.ajodo.2017.11.035.
<span class="bold">PMID: </span><a href="/pubmed/30075925" target="_blank">30075925</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29390172">Orthodontic treatment for deep bite and retroclined upper front teeth in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Millett DT,
Cunningham SJ,
O'Brien KD,
Benson PE,
de Oliveira CM</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Feb 1;2(2):CD005972.
doi: 10.1002/14651858.CD005972.pub4.
<span class="bold">PMID: </span><a href="/pubmed/29390172" target="_blank">29390172</a><a href="/pmc/articles/PMC6491166" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28968484">Orthodontic treatment for deep bite and retroclined upper front teeth in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Millett DT,
Cunningham SJ,
O'Brien KD,
Benson PE,
de Oliveira CM</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2017 Oct 2;10(10):CD005972.
doi: 10.1002/14651858.CD005972.pub3.
<span class="bold">PMID: </span><a href="/pubmed/28968484" target="_blank">28968484</a><a href="/pmc/articles/PMC6485795" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Increased%20overbite%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 (12)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/36901461">Bracket Bond Failures: Incidence and Association with Different Risk Factors-A Retrospective Study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Jakavičė R,
Kubiliūtė K,
Smailienė D</span><br />
<span class="medgenPMjournal">Int J Environ Res Public Health</span>
2023 Mar 2;20(5)
doi: 10.3390/ijerph20054452.
<span class="bold">PMID: </span><a href="/pubmed/36901461" target="_blank">36901461</a><a href="/pmc/articles/PMC10002450" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35843261">Are There Cephalometric Measurements Associated With Recurrent Temporomandibular Joint Dislocation?</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cohen A,
Rushinek H,
Sela MC,
Sharafan D,
Talisman S,
Casap N</span><br />
<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
2022 Oct;80(10):1587-1592.
Epub 2022 Jun 21
doi: 10.1016/j.joms.2022.06.005.
<span class="bold">PMID: </span><a href="/pubmed/35843261" target="_blank">35843261</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28083893">Malocclusion traits and oral health-related quality of life in Finnish adults.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Masood M,
Suominen AL,
Pietila T,
Lahti S</span><br />
<span class="medgenPMjournal">Community Dent Oral Epidemiol</span>
2017 Apr;45(2):178-188.
Epub 2017 Jan 12
doi: 10.1111/cdoe.12276.
<span class="bold">PMID: </span><a href="/pubmed/28083893" target="_blank">28083893</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26349294">Extreme Dental Compensation in an Adult Skeletal Class III Malocclusion: 3-Year Follow-up of a Successfully Compromised Treatment.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Estelita S,
Janson G,
Chiqueto K</span><br />
<span class="medgenPMjournal">Int J Orthod Milwaukee</span>
2015 Summer;26(2):69-76.
<span class="bold">PMID: </span><a href="/pubmed/26349294" target="_blank">26349294</a></div>
<div class="nl"><a target="_blank" href="/pubmed/9294357">Predicting functional appliance treatment outcome in Class II malocclusions--a review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Barton S,
Cook PA</span><br />
<span class="medgenPMjournal">Am J Orthod Dentofacial Orthop</span>
1997 Sep;112(3):282-6.
doi: 10.1016/S0889-5406(97)70257-9.
<span class="bold">PMID: </span><a href="/pubmed/9294357" target="_blank">9294357</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Increased%20overbite%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (15)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/35843261">Are There Cephalometric Measurements Associated With Recurrent Temporomandibular Joint Dislocation?</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cohen A,
Rushinek H,
Sela MC,
Sharafan D,
Talisman S,
Casap N</span><br />
<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
2022 Oct;80(10):1587-1592.
Epub 2022 Jun 21
doi: 10.1016/j.joms.2022.06.005.
<span class="bold">PMID: </span><a href="/pubmed/35843261" target="_blank">35843261</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28083893">Malocclusion traits and oral health-related quality of life in Finnish adults.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Masood M,
Suominen AL,
Pietila T,
Lahti S</span><br />
<span class="medgenPMjournal">Community Dent Oral Epidemiol</span>
2017 Apr;45(2):178-188.
Epub 2017 Jan 12
doi: 10.1111/cdoe.12276.
<span class="bold">PMID: </span><a href="/pubmed/28083893" target="_blank">28083893</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26892218">Caries Experience in Individuals with Moebius Syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Castro T,
Ortega AO,
Mussi MC,
Braga MM,
Gallottini M</span><br />
<span class="medgenPMjournal">Pediatr Dent</span>
2016 Jan-Feb;38(1):68-71.
<span class="bold">PMID: </span><a href="/pubmed/26892218" target="_blank">26892218</a></div>
<div class="nl"><a target="_blank" href="/pubmed/9294357">Predicting functional appliance treatment outcome in Class II malocclusions--a review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Barton S,
Cook PA</span><br />
<span class="medgenPMjournal">Am J Orthod Dentofacial Orthop</span>
1997 Sep;112(3):282-6.
doi: 10.1016/S0889-5406(97)70257-9.
<span class="bold">PMID: </span><a href="/pubmed/9294357" target="_blank">9294357</a></div>
<div class="nl"><a target="_blank" href="/pubmed/7676364">Sickle cell anemia: a review of the dental concerns and a retrospective study of dental and bony changes.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Taylor LB,
Nowak AJ,
Giller RH,
Casamassimo PS</span><br />
<span class="medgenPMjournal">Spec Care Dentist</span>
1995 Jan-Feb;15(1):38-42.
doi: 10.1111/j.1754-4505.1995.tb00469.x.
<span class="bold">PMID: </span><a href="/pubmed/7676364" target="_blank">7676364</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Increased%20overbite%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 (24)</a></div></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Millett DT,
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O'Brien KD,
Benson PE,
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<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2018 Feb 1;2(2):CD005972.
doi: 10.1002/14651858.CD005972.pub4.
<span class="bold">PMID: </span><a href="/pubmed/29390172" target="_blank">29390172</a><a href="/pmc/articles/PMC6491166" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28968484">Orthodontic treatment for deep bite and retroclined upper front teeth in children.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Millett DT,
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<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2017 Oct 2;10(10):CD005972.
doi: 10.1002/14651858.CD005972.pub3.
<span class="bold">PMID: </span><a href="/pubmed/28968484" target="_blank">28968484</a><a href="/pmc/articles/PMC6485795" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Increased%20overbite%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 (2)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0266063%5bDISCUI%5d&amp;filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (1)</a></li>
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