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<!--
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UID=237237
|
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ConceptID=C1397139
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Calcification of falx cerebri</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>237237</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.">C1397139</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>Calcification of the falx cerebri</td></tr>
|
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<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0005462">HP:0005462</a></td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln">The presence of calcium deposition in the falx cerebri. [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 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">Calcification of falx cerebri</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/868416" ref="tree=MeSH" title="MedGen record for Abnormal nervous system morphology">Abnormal nervous system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892343" ref="tree=MeSH" title="MedGen record for Morphological central nervous system abnormality">Morphological central nervous system abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/869332" ref="tree=MeSH" title="MedGen record for Abnormal meningeal morphology">Abnormal meningeal morphology</a></span><ul><li><span class="TLline"><a href="/medgen/869331" ref="tree=MeSH" title="MedGen record for Abnormal dura mater morphology">Abnormal dura mater morphology</a></span><ul><li><span class="TLline"><a href="/medgen/866891" ref="tree=MeSH" title="MedGen record for Abnormality of the falx cerebri">Abnormality of the falx cerebri</a></span><ul><li><span class="matched_ds">Calcification of falx cerebri</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_2554"><div><strong>Gorlin syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>2554</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.">C0004779</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Neoplastic Process</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Nevoid basal cell carcinoma syndrome (NBCCS) is characterized by the development of multiple jaw keratocysts, frequently beginning in the second decade of life, and/or basal cell carcinomas (BCCs), usually from the third decade onward. Many individuals have a recognizable appearance with macrocephaly, frontal bossing, coarse facial features, and facial milia. Most individuals have skeletal anomalies (e.g., bifid ribs, wedge-shaped vertebrae). Ectopic calcification, particularly in the falx, is present in 90% of affected individuals by age 30 years. Cardiac and ovarian fibromas occur in approximately 2% and 20% of individuals, respectively. Approximately 5% of all children with NBCCS develop medulloblastoma (primitive neuroectodermal tumor), generally the desmoplastic subtype. The risk of developing medulloblastoma is substantially higher in individuals with an SUFU pathogenic variant (33%) than in those with a PTCH1 pathogenic variant (<2%). Peak incidence is at age one to two years. Life expectancy in NBCCS is not significantly different from average.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/2554">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_82694"><div><strong>Marshall syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>82694</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.">C0265235</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Marshall syndrome (MRSHS) is characterized by midfacial hypoplasia, cleft palate, ocular anomalies including high myopia and cataracts, sensorineural hearing loss, short stature with spondyloepiphyseal dysplasia, and arthropathy. In contrast to Stickler syndrome type II, it has less severe eye findings but striking ocular hypertelorism, more pronounced maxillary hypoplasia, and ectodermal abnormalities (summary by Shanske et al., 1997 and Ala-Kokko and Shanske, 2009).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/82694">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_338595"><div><strong>Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>338595</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.">C1849011</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spondylometaepiphyseal dysplasia, short limb-hand type is an autosomal recessive disorder with clinical and radiologic features of disproportionate short stature, platyspondyly, abnormal epiphyses and metaphyses, shortening of the lower and upper limbs, short and broad fingers, and premature calcifications. The disorder is progressive with respect to the severity of the bowing of the lower limbs and the appearance of calcifications, with some patients being wheelchair-bound from age 11 years (Bargal et al., 2009).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/338595">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_350933"><div><strong>Acromelic frontonasal dysostosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>350933</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.">C1863616</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Verloes et al. (1992) described a rare variant of frontonasal dysplasia (see FND1, 136760), designated acromelic frontonasal dysplasia (AFND), in which similar craniofacial anomalies are associated with variable central nervous system malformations and limb defects including tibial hypoplasia/aplasia, talipes equinovarus, and preaxial polydactyly of the feet.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/350933">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_357280"><div><strong>Pseudoxanthoma elasticum, forme fruste</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>357280</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.">C1867450</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Pseudoxanthoma elasticum (PXE) is a systemic disorder that affects the elastic tissue of the skin, the eye, and vascular system. Individuals most commonly present with angioid streaks of the retina found on routine eye examination or associated with retinal hemorrhage and/or characteristic papules in the skin. The most frequent cause of morbidity and disability in PXE is reduced vision due to complications of subretinal neovascularizations and macular atrophy. Other manifestations include premature gastrointestinal angina and/or bleeding, intermittent claudication of arm and leg muscles, stroke, renovascular hypertension, and cardiovascular complications (angina/myocardial infarction). Most affected individuals live a normal life span.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/357280">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1841087"><div><strong>Basal cell nevus syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1841087</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.">C5830451</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Neoplastic Process</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The basal cell nevus syndrome (BCNS), also known as Gorlin syndrome, is characterized by numerous basal cell cancers and epidermal cysts of the skin, calcified dural folds, keratocysts of the jaws, palmar and plantar pits, ovarian fibromas, medulloblastomas, lymphomesenteric cysts, fetal rhabdomyomas, and various stigmata of maldevelopment (e.g., rib and vertebral abnormalities, cleft lip or cleft palate, and cortical defects of bones) (summary by Koch et al., 2002). For a discussion of genetic heterogeneity of BCNS, see BCNS1 (109400).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1841087">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_350933" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acromelic frontonasal dysostosis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1841087" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Basal cell nevus syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_2554" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Gorlin syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_82694" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Marshall syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_357280" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pseudoxanthoma elasticum, forme fruste</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_338595" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38030746">Cranial midline shift is a predictor of the clinical prognosis of acute cerebral infarction patients undergoing emergency endovascular treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xu XM,
|
||
Zhang H,
|
||
Meng RL</span><br />
|
||
<span class="medgenPMjournal">Sci Rep</span>
|
||
2023 Nov 29;13(1):21037.
|
||
doi: 10.1038/s41598-023-48401-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38030746" target="_blank">38030746</a><a href="/pmc/articles/PMC10687008" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21503706">The usefulness of multidetector computed tomographic angiography for the diagnosis of Marfan syndrome by Ghent criteria.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sohn GH,
|
||
Jang SY,
|
||
Moon JR,
|
||
Yang JH,
|
||
Sung K,
|
||
Ki CS,
|
||
Oh JK,
|
||
Choe YH,
|
||
Kim DK</span><br />
|
||
<span class="medgenPMjournal">Int J Cardiovasc Imaging</span>
|
||
2011 Jun;27(5):679-88.
|
||
Epub 2011 Apr 19
|
||
doi: 10.1007/s10554-011-9867-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21503706" target="_blank">21503706</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1485214">Detection and management of gangliogliomas in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Otsubo H,
|
||
Hoffman HJ,
|
||
Humphreys RP,
|
||
Hendrick EB,
|
||
Drake JM,
|
||
Hwang PA,
|
||
Becker LE,
|
||
Chuang SH</span><br />
|
||
<span class="medgenPMjournal">Surg Neurol</span>
|
||
1992 Nov;38(5):371-8.
|
||
doi: 10.1016/0090-3019(92)90024-h.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1485214" target="_blank">1485214</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(calcification%20of%20falx%20cerebri)%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 (3)</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/22742575">Nevoid basal cell carcinoma syndrome: a 40-year study in the South African population.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Titinchi F,
|
||
Nortje CJ,
|
||
Parker ME,
|
||
van Rensburg LJ</span><br />
|
||
<span class="medgenPMjournal">J Oral Pathol Med</span>
|
||
2013 Feb;42(2):162-5.
|
||
Epub 2012 Jun 28
|
||
doi: 10.1111/j.1600-0714.2012.01188.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22742575" target="_blank">22742575</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22669069">Nevoid basal cell carcinoma syndrome in Indian patients: a clinical and radiological study of 6 cases and review of literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gupta SR,
|
||
Jaetli V,
|
||
Mohanty S,
|
||
Sharma R,
|
||
Gupta A</span><br />
|
||
<span class="medgenPMjournal">Oral Surg Oral Med Oral Pathol Oral Radiol</span>
|
||
2012 Jan;113(1):99-110.
|
||
Epub 2012 Feb 3
|
||
doi: 10.1016/j.tripleo.2011.08.017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22669069" target="_blank">22669069</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21189772">Nevoid basal cell carcinoma syndrome presenting with neck pits and café au lait patches.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Balasundram S,
|
||
Kovilpillai FJ,
|
||
Hopper C</span><br />
|
||
<span class="medgenPMjournal">J Clin Pediatr Dent</span>
|
||
2010 Fall;35(1):95-100.
|
||
doi: 10.17796/jcpd.35.1.r7t6t25372830426.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21189772" target="_blank">21189772</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20502085">Multiple odontogenic keratocysts associated with Gorlin-Goltz syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dixit S,
|
||
Acharya S,
|
||
Dixit PB</span><br />
|
||
<span class="medgenPMjournal">Kathmandu Univ Med J (KUMJ)</span>
|
||
2009 Oct-Dec;7(28):414-8.
|
||
doi: 10.3126/kumj.v7i4.2765.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20502085" target="_blank">20502085</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Calcification%20of%20falx%20cerebri%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 (4)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30995852">Gorlin-Goltz syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bartoš V,
|
||
Kullová M,
|
||
Adamicová K,
|
||
Paučinová I</span><br />
|
||
<span class="medgenPMjournal">Klin Onkol</span>
|
||
2019 Spring;32(2):124-128.
|
||
doi: 10.14735/amko2019124.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30995852" target="_blank">30995852</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29806651">The relevance of dental surgeon on Gorlin-Goltz syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Trento GDS,
|
||
Gorla LFO,
|
||
Navarro CM,
|
||
Filho VAP</span><br />
|
||
<span class="medgenPMjournal">Stomatologija</span>
|
||
2017;19(4):130-132.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29806651" target="_blank">29806651</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26297769">Gorlin-Goltz syndrome in twin brothers: an unusual occurrence with review of the literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Anchlia S,
|
||
Vyas S,
|
||
Bahl S,
|
||
Nagavadiya V</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2015 Aug 21;2015
|
||
doi: 10.1136/bcr-2015-211608.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26297769" target="_blank">26297769</a><a href="/pmc/articles/PMC4551002" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24010868">Hajdu-cheney syndrome with osteomyelitis of mandible, calcification of falx cerebri and palatal groove.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gupta SR,
|
||
Gupta R</span><br />
|
||
<span class="medgenPMjournal">Cleft Palate Craniofac J</span>
|
||
2014 Nov;51(6):722-8.
|
||
Epub 2013 Sep 6
|
||
doi: 10.1597/13-021.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24010868" target="_blank">24010868</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22742575">Nevoid basal cell carcinoma syndrome: a 40-year study in the South African population.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Titinchi F,
|
||
Nortje CJ,
|
||
Parker ME,
|
||
van Rensburg LJ</span><br />
|
||
<span class="medgenPMjournal">J Oral Pathol Med</span>
|
||
2013 Feb;42(2):162-5.
|
||
Epub 2012 Jun 28
|
||
doi: 10.1111/j.1600-0714.2012.01188.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22742575" target="_blank">22742575</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Calcification%20of%20falx%20cerebri%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 (9)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30995852">Gorlin-Goltz syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bartoš V,
|
||
Kullová M,
|
||
Adamicová K,
|
||
Paučinová I</span><br />
|
||
<span class="medgenPMjournal">Klin Onkol</span>
|
||
2019 Spring;32(2):124-128.
|
||
doi: 10.14735/amko2019124.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30995852" target="_blank">30995852</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21189772">Nevoid basal cell carcinoma syndrome presenting with neck pits and café au lait patches.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Balasundram S,
|
||
Kovilpillai FJ,
|
||
Hopper C</span><br />
|
||
<span class="medgenPMjournal">J Clin Pediatr Dent</span>
|
||
2010 Fall;35(1):95-100.
|
||
doi: 10.17796/jcpd.35.1.r7t6t25372830426.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21189772" target="_blank">21189772</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20502085">Multiple odontogenic keratocysts associated with Gorlin-Goltz syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dixit S,
|
||
Acharya S,
|
||
Dixit PB</span><br />
|
||
<span class="medgenPMjournal">Kathmandu Univ Med J (KUMJ)</span>
|
||
2009 Oct-Dec;7(28):414-8.
|
||
doi: 10.3126/kumj.v7i4.2765.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20502085" target="_blank">20502085</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Calcification%20of%20falx%20cerebri%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/10066029">Nevoid basal cell carcinoma syndrome. Clinical findings in 37 Italian affected individuals.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lo Muzio L,
|
||
Nocini PF,
|
||
Savoia A,
|
||
Consolo U,
|
||
Procaccini M,
|
||
Zelante L,
|
||
Pannone G,
|
||
Bucci P,
|
||
Dolci M,
|
||
Bambini F,
|
||
Solda P,
|
||
Favia G</span><br />
|
||
<span class="medgenPMjournal">Clin Genet</span>
|
||
1999 Jan;55(1):34-40.
|
||
doi: 10.1034/j.1399-0004.1999.550106.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10066029" target="_blank">10066029</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Calcification%20of%20falx%20cerebri%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 (1)</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 -->
|
||
<div class="rightCol mgCol">
|
||
<div class="portlet mgSection" id="ID_113">
|
||
<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>
|
||
<div class="portlet_content ln"><ul id="my-toc"></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_119">
|
||
<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>
|
||
<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Calcification%20of%20falx%20cerebri" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_121">
|
||
<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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