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<meta name="keywords" content="C1866710, absent pubic ossification (infancy), absent pubic ossification in infancy, delayed maturation of pubic bone, delayed mineralization of pubic bone, delayed ossification of pubic bone, delayed pubic bone ossification, finding, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="Delayed maturation and calcification of the pubic bone." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Delayed pubic bone ossification (Concept Id: C1866710)
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<!--
UID=357116
ConceptID=C1866710
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Delayed pubic bone ossification</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>357116</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.">C1866710</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
<td>Absent pubic ossification (infancy); Delayed ossification of pubic bone</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:0008788">HP:0008788</a></td></tr>
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<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">Delayed maturation and calcification of the pubic bone. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
</div>
<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 unavailable round" title="Clinical test">C</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">Delayed pubic bone ossification</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/868760" ref="tree=MeSH" title="MedGen record for Abnormal skeletal morphology">Abnormal skeletal morphology</a></span><ul><li><span class="TLline"><a href="/medgen/871157" ref="tree=MeSH" title="MedGen record for Abnormal bone structure">Abnormal bone structure</a></span><ul><li><span class="TLline"><a href="/medgen/868756" ref="tree=MeSH" title="MedGen record for Abnormal bone ossification">Abnormal bone ossification</a></span><ul><li><span class="TLline"><a href="/medgen/871155" ref="tree=MeSH" title="MedGen record for Abnormal enchondral ossification">Abnormal enchondral ossification</a></span><ul><li><span class="TLline"><a href="/medgen/867167" ref="tree=MeSH" title="MedGen record for Abnormal pelvis bone ossification">Abnormal pelvis bone ossification</a></span><ul><li><span class="TLline"><a href="/medgen/870163" ref="tree=MeSH" title="MedGen record for Abnormal ossification of the pubic bone">Abnormal ossification of the pubic bone</a></span><ul><li><span class="matched_ds">Delayed pubic bone ossification</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_3486"><div><strong>Cleidocranial dysostosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>3486</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.">C0008928</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Cleidocranial dysplasia (CCD) spectrum disorder is a skeletal dysplasia that represents a clinical continuum ranging from classic CCD (triad of delayed closure of the cranial sutures, hypoplastic or aplastic clavicles, and dental abnormalities), to mild CCD, to isolated dental anomalies without other skeletal features. Individuals with classic CCD spectrum disorder typically have abnormally large, wide-open fontanelles at birth that may remain open throughout life. Clavicular hypoplasia can result in narrow, sloping shoulders that can be opposed at the midline. Moderate short stature may be observed, with most affected individuals being shorter than their unaffected sibs. Dental anomalies may include delayed eruption of secondary dentition, failure to shed the primary teeth, and supernumerary teeth. Individuals with CCD spectrum disorder are at increased risk of developing recurrent sinus infections, recurrent ear infections leading to conductive hearing loss, and upper airway obstruction. Intelligence is typically normal.</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/3486">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_147134"><div><strong>Spondyloepimetaphyseal dysplasia, Strudwick type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>147134</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.">C0700635</a></dd><dt><span class="dotprefix"></span></dt><dd>Finding</dd></dl></div></div></div>
<div class="spaceAbove">The Strudwick type of spondyloepimetaphyseal dysplasia (SEMD) is characterized by disproportionate short stature, pectus carinatum, and scoliosis, as well as dappled metaphyses (summary by Tiller et al., 1995).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/147134">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_412530"><div><strong>Spondyloepiphyseal dysplasia congenita</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>412530</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.">C2745959</a></dd><dt><span class="dotprefix"></span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
<div class="spaceAbove">Spondyloepiphyseal dysplasia congenita (SEDC) is an autosomal dominant chondrodysplasia characterized by disproportionate short stature (short trunk), abnormal epiphyses, and flattened vertebral bodies. Skeletal features are manifested at birth and evolve with time. Other features include myopia and/or retinal degeneration with retinal detachment and cleft palate (summary by Anderson et al., 1990).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/412530">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_412869"><div><strong>Spondylo-megaepiphyseal-metaphyseal dysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>412869</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.">C2750066</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Spondylo-megaepiphyseal-metaphyseal dysplasia is a rare autosomal recessive skeletal dysplasia characterized by disproportionate short stature with a short and stiff neck and trunk; relatively long limbs that may show flexion contractures of the distal joints; delayed and impaired ossification of the vertebral bodies and the presence of large epiphyseal ossification centers and wide growth plates in the long tubular bones; and numerous pseudoepiphyses of the short tubular bones in hands and feet (summary by Hellemans et al., 2009).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/412869">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1648323"><div><strong>Spondyloepimetaphyseal dysplasia, Krakow type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1648323</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.">C4748455</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Krakow-type spondyloepimetaphyseal dysplasia is characterized by severe skeletal dysplasia, severe immunodeficiency, and developmental delay (Csukasi et al., 2018).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1648323">Condition Record</a></div></div>
<div class="divPopper rprt" id="rdis_1824016"><div><strong>Cleidocranial dysplasia 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1824016</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.">C5774243</a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
<div class="spaceAbove">Cleidocranial dysplasia-2 (CLCD2) is characterized by clavicular anomalies, ranging from unilateral 'clavicula bipartita' to bilateral clavicular aplasia, and dental anomalies, including delayed or absent eruption of deciduous teeth and supernumerary teeth. Skull abnormalities such as delayed closure of fontanels have been reported; other skeletal features include delayed bone age, short distal phalanges, and pseudoepiphyses of the metacarpals and/or metatarsals. Phenotypic variability, including intrafamilial, has been observed (Beyltjens et al., 2023).&#13; For a general phenotypic description and a discussion of genetic heterogeneity of cleidocranial dysplasia, see CLCD1 (119600).</div>
<div class="spaceAbove nowrap">See: <a href="/medgen/1824016">Condition Record</a></div></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_3486" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cleidocranial dysostosis</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1824016" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cleidocranial dysplasia 2</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_412869" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondylo-megaepiphyseal-metaphyseal dysplasia</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1648323" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondyloepimetaphyseal dysplasia, Krakow type</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_147134" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondyloepimetaphyseal dysplasia, Strudwick type</a></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_412530" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondyloepiphyseal dysplasia congenita</a></div></div>
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<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>
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<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/38664181">Bilateral Obturator Osteotomy: A Novel Osteotomy for Bladder Exstrophy Closure.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Faraj S,
Decante C,
Alliot H,
Hamel A,
Leclair MD</span><br />
<span class="medgenPMjournal">J Pediatr Surg</span>
2024 Sep;59(9):1841-1845.
Epub 2024 Apr 2
doi: 10.1016/j.jpedsurg.2024.03.058.
<span class="bold">PMID: </span><a href="/pubmed/38664181" target="_blank">38664181</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33992513">Mid-term follow-up of superior pubic ramus osteotomy in locked symphysis pubis with urethral injury: A case report.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Basu A,
Shukla N,
Velagada S,
Behera S</span><br />
<span class="medgenPMjournal">Chin J Traumatol</span>
2023 Jul;26(4):244-248.
Epub 2021 Apr 2
doi: 10.1016/j.cjtee.2021.03.008.
<span class="bold">PMID: </span><a href="/pubmed/33992513" target="_blank">33992513</a><a href="/pmc/articles/PMC10388251" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30701593">Assessing the fusion of the ischiopubic synchondrosis using predictive modeling.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gregory LS,
Jones LV,
Amorosi NM</span><br />
<span class="medgenPMjournal">Clin Anat</span>
2019 Sep;32(6):851-859.
Epub 2019 Feb 22
doi: 10.1002/ca.23345.
<span class="bold">PMID: </span><a href="/pubmed/30701593" target="_blank">30701593</a></div>
<div class="nl"><a target="_blank" href="/pubmed/17444568">Contribution of three-dimensional computed tomography in the assessment of fetal skeletal dysplasia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cassart M,
Massez A,
Cos T,
Tecco L,
Thomas D,
Van Regemorter N,
Avni F</span><br />
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
2007 May;29(5):537-43.
doi: 10.1002/uog.4001.
<span class="bold">PMID: </span><a href="/pubmed/17444568" target="_blank">17444568</a></div>
<div class="nl"><a target="_blank" href="/pubmed/221875">The non-ossified pubis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cortina H,
Vallcanera A,
Andres V,
Gracia A,
Aparici R,
Mari A</span><br />
<span class="medgenPMjournal">Pediatr Radiol</span>
1979 Apr 19;8(2):87-92.
doi: 10.1007/BF00973997.
<span class="bold">PMID: </span><a href="/pubmed/221875" target="_blank">221875</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Delayed%20pubic%20bone%20ossification%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 (6)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/29987841">Report of second case and clinical and molecular characterization of Eiken syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Moirangthem A,
Narayanan DL,
Jacob P,
Nishimura G,
Mortier G,
Girisha KM</span><br />
<span class="medgenPMjournal">Clin Genet</span>
2018 Nov;94(5):457-460.
Epub 2018 Jul 27
doi: 10.1111/cge.13413.
<span class="bold">PMID: </span><a href="/pubmed/29987841" target="_blank">29987841</a></div>
<div class="nl"><a target="_blank" href="/pubmed/22387057">Clinical and radiological findings in Pallister-Killian syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Jamuar S,
Lai A,
Unger S,
Nishimura G</span><br />
<span class="medgenPMjournal">Eur J Med Genet</span>
2012 Mar;55(3):167-72.
Epub 2012 Feb 10
doi: 10.1016/j.ejmg.2012.01.019.
<span class="bold">PMID: </span><a href="/pubmed/22387057" target="_blank">22387057</a></div>
<div class="nl"><a target="_blank" href="/pubmed/17444568">Contribution of three-dimensional computed tomography in the assessment of fetal skeletal dysplasia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cassart M,
Massez A,
Cos T,
Tecco L,
Thomas D,
Van Regemorter N,
Avni F</span><br />
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
2007 May;29(5):537-43.
doi: 10.1002/uog.4001.
<span class="bold">PMID: </span><a href="/pubmed/17444568" target="_blank">17444568</a></div>
<div class="nl"><a target="_blank" href="/pubmed/14689542">Prenatal diagnosis of a cleidocranial dysplasia-like phenotype associated with a de novo balanced t(2q;6q)(q36;q16) translocation.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Winer N,
Le Caignec C,
Quere MP,
David A,
Boceno M,
Aubron F,
Joubert M,
Boog G,
Philippe HJ,
Rival JM</span><br />
<span class="medgenPMjournal">Ultrasound Obstet Gynecol</span>
2003 Dec;22(6):648-51.
doi: 10.1002/uog.916.
<span class="bold">PMID: </span><a href="/pubmed/14689542" target="_blank">14689542</a></div>
<div class="nl"><a target="_blank" href="/pubmed/12424591">Severe cleidocranial dysplasia can mimic hypophosphatasia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Unger S,
Mornet E,
Mundlos S,
Blaser S,
Cole DE</span><br />
<span class="medgenPMjournal">Eur J Pediatr</span>
2002 Nov;161(11):623-6.
Epub 2002 Jun 28
doi: 10.1007/s00431-002-0978-9.
<span class="bold">PMID: </span><a href="/pubmed/12424591" target="_blank">12424591</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Delayed%20pubic%20bone%20ossification%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 (5)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/33992513">Mid-term follow-up of superior pubic ramus osteotomy in locked symphysis pubis with urethral injury: A case report.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Basu A,
Shukla N,
Velagada S,
Behera S</span><br />
<span class="medgenPMjournal">Chin J Traumatol</span>
2023 Jul;26(4):244-248.
Epub 2021 Apr 2
doi: 10.1016/j.cjtee.2021.03.008.
<span class="bold">PMID: </span><a href="/pubmed/33992513" target="_blank">33992513</a><a href="/pmc/articles/PMC10388251" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30701593">Assessing the fusion of the ischiopubic synchondrosis using predictive modeling.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gregory LS,
Jones LV,
Amorosi NM</span><br />
<span class="medgenPMjournal">Clin Anat</span>
2019 Sep;32(6):851-859.
Epub 2019 Feb 22
doi: 10.1002/ca.23345.
<span class="bold">PMID: </span><a href="/pubmed/30701593" target="_blank">30701593</a></div>
<div class="nl"><a target="_blank" href="/pubmed/17506107">Expanding spectrum of congenital disorder of glycosylation Ig (CDG-Ig): sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kranz C,
Basinger AA,
Güçsavaş-Calikoğlu M,
Sun L,
Powell CM,
Henderson FW,
Aylsworth AS,
Freeze HH</span><br />
<span class="medgenPMjournal">Am J Med Genet A</span>
2007 Jun 15;143A(12):1371-8.
doi: 10.1002/ajmg.a.31791.
<span class="bold">PMID: </span><a href="/pubmed/17506107" target="_blank">17506107</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Delayed%20pubic%20bone%20ossification%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 (3)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/38664181">Bilateral Obturator Osteotomy: A Novel Osteotomy for Bladder Exstrophy Closure.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Faraj S,
Decante C,
Alliot H,
Hamel A,
Leclair MD</span><br />
<span class="medgenPMjournal">J Pediatr Surg</span>
2024 Sep;59(9):1841-1845.
Epub 2024 Apr 2
doi: 10.1016/j.jpedsurg.2024.03.058.
<span class="bold">PMID: </span><a href="/pubmed/38664181" target="_blank">38664181</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30701593">Assessing the fusion of the ischiopubic synchondrosis using predictive modeling.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gregory LS,
Jones LV,
Amorosi NM</span><br />
<span class="medgenPMjournal">Clin Anat</span>
2019 Sep;32(6):851-859.
Epub 2019 Feb 22
doi: 10.1002/ca.23345.
<span class="bold">PMID: </span><a href="/pubmed/30701593" target="_blank">30701593</a></div>
<div class="nl"><a target="_blank" href="/pubmed/29987841">Report of second case and clinical and molecular characterization of Eiken syndrome.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Moirangthem A,
Narayanan DL,
Jacob P,
Nishimura G,
Mortier G,
Girisha KM</span><br />
<span class="medgenPMjournal">Clin Genet</span>
2018 Nov;94(5):457-460.
Epub 2018 Jul 27
doi: 10.1111/cge.13413.
<span class="bold">PMID: </span><a href="/pubmed/29987841" target="_blank">29987841</a></div>
<div class="nl"><a target="_blank" href="/pubmed/14736662">Asymmetric closure of ischiopubic synchondrosis in pediatric patients: correlation with foot dominance.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Herneth AM,
Philipp MO,
Pretterklieber ML,
Balassy C,
Winkelbauer FW,
Beaulieu CF</span><br />
<span class="medgenPMjournal">AJR Am J Roentgenol</span>
2004 Feb;182(2):361-5.
doi: 10.2214/ajr.182.2.1820361.
<span class="bold">PMID: </span><a href="/pubmed/14736662" target="_blank">14736662</a></div>
<div class="nl"><a target="_blank" href="/pubmed/221875">The non-ossified pubis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cortina H,
Vallcanera A,
Andres V,
Gracia A,
Aparici R,
Mari A</span><br />
<span class="medgenPMjournal">Pediatr Radiol</span>
1979 Apr 19;8(2):87-92.
doi: 10.1007/BF00973997.
<span class="bold">PMID: </span><a href="/pubmed/221875" target="_blank">221875</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Delayed%20pubic%20bone%20ossification%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 (5)</a></div></div>
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