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1102 lines
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<meta name="keywords" content="C0021933, disease or syndrome, intestinal intussusception, intestinal invagination, intestinal invaginations, intussusception, intussusception (morphologic abnormality), intussusception of intestine, intussusception of the intestine, intussusceptions, intususception, intususceptions, invagination of intestine, invagination of intestine or colon, invagination, intestinal, invaginations, intestinal, isn - intussusception, 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="An abnormality of the intestine in which part of the intestine invaginates (telescopes) into another part of the intestine." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
|
||
UID=43940
|
||
ConceptID=C0021933
|
||
-->
|
||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Intussusception</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>43940</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.">C0021933</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Intestinal Invagination; Intestinal Invaginations; Intussusceptions; Intususception; Intususceptions; Invagination, Intestinal; Invaginations, Intestinal</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>ISN - Intussusception (49723003); Intussusception of the intestine (49723003); Intestinal intussusception (49723003); Intussusception of intestine (49723003); Invagination of intestine (49723003)</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:0002576">HP:0002576</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0007835" target="_blank">MONDO:0007835</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/147710" target="_blank">147710</a></td></tr>
|
||
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_100">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln">An abnormality of the intestine in which part of the intestine invaginates (telescopes) into another part of the intestine. [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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||
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<div class="portlet mgSection" id="ID_102">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
|
||
<div class="divPopper rprt" id="clin_43940"><div><strong>Intussusception</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>43940</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.">C0021933</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An abnormality of the intestine in which part of the intestine invaginates (telescopes) into another part of the intestine.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/43940">Feature record</a> | <a href="/medgen?term=%22Intussusception%22%5BClinical%20Features%5D%20OR%2043940%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite"><ul><li><span class="TLline">Abnormality of the digestive system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_43940" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intussusception</a></span></li></ul></li></ul></div></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 Ocolor" title="OMIM"><a ref="ncbi_uid=43940" target="_blank" href="/omim/147710">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Intussusception</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/3828" ref="tree=MeSH" title="MedGen record for Disorder of digestive system">Disorder of digestive system</a></span><ul><li><span class="TLline"><a href="/medgen/78584" ref="tree=MeSH" title="MedGen record for Abnormality of the digestive system">Abnormality of the digestive system</a></span><ul><li><span class="TLline"><a href="/medgen/927600" ref="tree=MeSH" title="MedGen record for Abnormal digestive system morphology">Abnormal digestive system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/866726" ref="tree=MeSH" title="MedGen record for Abnormal gastrointestinal tract morphology">Abnormal gastrointestinal tract morphology</a></span><ul><li><span class="TLline"><a href="/medgen/1388201" ref="tree=MeSH" title="MedGen record for Abnormal intestine morphology">Abnormal intestine morphology</a></span><ul><li><span class="matched_ds">Intussusception</span><ul><li><span class="TLline"><a href="/medgen/1779818" ref="tree=MeSH" title="MedGen record for Ileoileal intussusception">Ileoileal intussusception</a></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_43940"><div><strong>Intussusception</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>43940</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.">C0021933</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An abnormality of the intestine in which part of the intestine invaginates (telescopes) into another part of the intestine.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/43940">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_18404"><div><strong>Peutz-Jeghers syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>18404</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.">C0031269</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Peutz-Jeghers syndrome (PJS) is characterized by the association of gastrointestinal (GI) polyposis, mucocutaneous pigmentation, and cancer predisposition. PJS-type hamartomatous polyps are most common in the small intestine (in order of prevalence: jejunum, ileum, and duodenum) but can also occur in the stomach, large bowel, and extraintestinal sites including the renal pelvis, bronchus, gall bladder, nasal passages, urinary bladder, and ureters. GI polyps can result in chronic bleeding, anemia, and recurrent obstruction and intussusception requiring repeated laparotomy and bowel resection. Mucocutaneous hyperpigmentation presents in childhood as dark blue to dark brown macules around the mouth, eyes, and nostrils, in the perianal area, and on the buccal mucosa. Hyperpigmented macules on the fingers are common. The macules may fade in puberty and adulthood. Recognition of the distinctive skin manifestations is important especially in individuals who have PJS as the result of a de novo pathogenic variant as these skin findings often predate GI signs and symptoms. Individuals with PJS are at increased risk for a wide variety of epithelial malignancies (colorectal, gastric, pancreatic, breast, and ovarian cancers). Females are at risk for sex cord tumors with annular tubules (SCTAT), a benign neoplasm of the ovaries, and adenoma malignum of the cervix, a rare aggressive cancer. Males occasionally develop large calcifying Sertoli cell tumors of the testes, which secrete estrogen and can lead to gynecomastia, advanced skeletal age, and ultimately short stature, if untreated.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/18404">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_87518"><div><strong>Juvenile polyposis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>87518</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.">C0345893</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Neoplastic Process</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Juvenile polyposis syndrome (JPS) is characterized by predisposition to hamartomatous polyps in the gastrointestinal (GI) tract, specifically in the stomach, small intestine, colon, and rectum. The term "juvenile" refers to the type of polyp rather than to the age of onset of polyps. Most individuals with JPS have some polyps by age 20 years; some may have only four or five polyps over their lifetime, whereas others in the same family may have more than 100. If the polyps are left untreated, they may cause bleeding and anemia. Most juvenile polyps are benign; however, malignant transformation can occur. Risk for GI cancers ranges from 11% to 86%. Most of this increased risk is attributed to colon cancer, but cancers of the stomach, upper GI tract, and pancreas have also been reported. A combined syndrome of JPS and hereditary hemorrhagic telangiectasia (HHT) is present in most individuals with an SMAD4 pathogenic variant.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/87518">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_83401"><div><strong>Blue rubber bleb nevus</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>83401</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.">C0346072</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare vascular malformation disorder with cutaneous and visceral lesions frequently associated with serious, potentially fatal bleeding and anemia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/83401">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_481620"><div><strong>Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>481620</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.">C3279990</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">IMD31C is a disorder of immunologic dysregulation with highly variable manifestations resulting from autosomal dominant gain-of-function mutations in STAT1 (600555). Most patients present in infancy or early childhood with chronic mucocutaneous candidiasis (CMC). Other highly variable features include recurrent bacterial, viral, fungal, and mycoplasmal infections, disseminated dimorphic fungal infections, enteropathy with villous atrophy, and autoimmune disorders, such as hypothyroidism or diabetes mellitus. A subset of patients show apparently nonimmunologic features, including osteopenia, delayed puberty, and intracranial aneurysms. Laboratory studies show increased activation of gamma-interferon (IFNG; 147570)-mediated inflammation (summary by Uzel et al., 2013 and Sampaio et al., 2013).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/481620">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_482428"><div><strong>Cutis laxa, autosomal recessive, type 1B</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>482428</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.">C3280798</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">EFEMP2-related cutis laxa, or autosomal recessive cutis laxa type 1B (ARCL1B), is characterized by cutis laxa and systemic involvement, most commonly arterial tortuosity, aneurysms, and stenosis; retrognathia; joint laxity; and arachnodactyly. Severity ranges from perinatal lethality as a result of cardiopulmonary failure to manifestations limited to the vascular and craniofacial systems.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/482428">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_482831"><div><strong>Coffin-Siris syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>482831</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.">C3281201</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Coffin-Siris syndrome (CSS) is classically characterized by aplasia or hypoplasia of the distal phalanx or nail of the fifth and additional digits, developmental or cognitive delay of varying degree, distinctive facial features, hypotonia, hirsutism/hypertrichosis, and sparse scalp hair. Congenital anomalies can include malformations of the cardiac, gastrointestinal, genitourinary, and/or central nervous systems. Other findings commonly include feeding difficulties, slow growth, ophthalmologic abnormalities, and hearing impairment.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/482831">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1677803"><div><strong>Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1677803</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.">C5193005</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">GIST-plus syndrome (GISTPS) is an autosomal dominant disorder characterized by incomplete penetrance of multiple mesenchymal tumors of the gastrointestinal tract, including gastrointestinal stromal tumor (GIST), inflammatory fibroid polyps (IFP), and fibroid tumors (FT). Some patients have been reported with coarse facies and skin, broad hands and feet, and premature tooth loss. Isolated GISTs and IFPs are seen in patients with somatic PDGFRA mutations (summary by Manley et al., 2018).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1677803">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_481620" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_83401" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Blue rubber bleb nevus</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_482831" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Coffin-Siris syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_482428" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cutis laxa, autosomal recessive, type 1B</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_43940" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intussusception</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_87518" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Juvenile polyposis syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_18404" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Peutz-Jeghers syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1677803" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal</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/37054692">Clinical Guidelines for Diagnosis and Management of Peutz-Jeghers Syndrome in Children and Adults.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yamamoto H,
|
||
Sakamoto H,
|
||
Kumagai H,
|
||
Abe T,
|
||
Ishiguro S,
|
||
Uchida K,
|
||
Kawasaki Y,
|
||
Saida Y,
|
||
Sano Y,
|
||
Takeuchi Y,
|
||
Tajika M,
|
||
Nakajima T,
|
||
Banno K,
|
||
Funasaka Y,
|
||
Hori S,
|
||
Yamaguchi T,
|
||
Yoshida T,
|
||
Ishikawa H,
|
||
Iwama T,
|
||
Okazaki Y,
|
||
Saito Y,
|
||
Matsuura N,
|
||
Mutoh M,
|
||
Tomita N,
|
||
Akiyama T,
|
||
Yamamoto T,
|
||
Ishida H,
|
||
Nakayama Y</span><br />
|
||
<span class="medgenPMjournal">Digestion</span>
|
||
2023;104(5):335-347.
|
||
Epub 2023 Apr 13
|
||
doi: 10.1159/000529799.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37054692" target="_blank">37054692</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31981391">Appendix intussusception: a challenging differential diagnosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Grama F,
|
||
Onica M,
|
||
Chitul A,
|
||
Bezede C,
|
||
Burcoș T,
|
||
Cristian D</span><br />
|
||
<span class="medgenPMjournal">ANZ J Surg</span>
|
||
2020 Oct;90(10):2090-2091.
|
||
Epub 2020 Jan 25
|
||
doi: 10.1111/ans.15727.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31981391" target="_blank">31981391</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22962878">Gastroenteritis in children: Part II. Prevention and management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Churgay CA,
|
||
Aftab Z</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2012 Jun 1;85(11):1066-70.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22962878" target="_blank">22962878</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22intussusception%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 (224)</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/35713304">Incidence of Intussusception in Bamako, Mali, Before and After the Introduction of Rotavirus Vaccine.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Roose A,
|
||
Keita AM,
|
||
Tapia MD,
|
||
Sow SO,
|
||
Mast TC,
|
||
Kotloff KL</span><br />
|
||
<span class="medgenPMjournal">J Pediatric Infect Dis Soc</span>
|
||
2022 Sep 29;11(9):404-407.
|
||
doi: 10.1093/jpids/piac044.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35713304" target="_blank">35713304</a><a href="/pmc/articles/PMC9520282" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21062662">Cecocolic intussusception.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tominaga K,
|
||
Kato M,
|
||
Kitagawa T,
|
||
Saida Y,
|
||
Gomi T,
|
||
Maetani I</span><br />
|
||
<span class="medgenPMjournal">Gastrointest Endosc</span>
|
||
2011 Apr;73(4):818-9.
|
||
Epub 2010 Nov 9
|
||
doi: 10.1016/j.gie.2010.09.038.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21062662" target="_blank">21062662</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14534754">Intussusception. Part 3: Diagnosis and management of those with an identifiable or predisposing cause and those that reduce spontaneously.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Navarro O,
|
||
Daneman A</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
2004 Apr;34(4):305-12; quiz 369.
|
||
Epub 2003 Oct 8
|
||
doi: 10.1007/s00247-003-1028-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14534754" target="_blank">14534754</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2400224">Intussusception: factors related to treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Reijnen JA,
|
||
Festen C,
|
||
van Roosmalen RP</span><br />
|
||
<span class="medgenPMjournal">Arch Dis Child</span>
|
||
1990 Aug;65(8):871-3.
|
||
doi: 10.1136/adc.65.8.871.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2400224" target="_blank">2400224</a><a href="/pmc/articles/PMC1792509" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2359000">The leadpoint in intussusception.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ong NT,
|
||
Beasley SW</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Surg</span>
|
||
1990 Jun;25(6):640-3.
|
||
doi: 10.1016/0022-3468(90)90353-b.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2359000" target="_blank">2359000</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Intussusception%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 (2038)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36652357">Colocolonic Intussusception.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yi G,
|
||
Li J</span><br />
|
||
<span class="medgenPMjournal">N Engl J Med</span>
|
||
2023 Jan 19;388(3):263.
|
||
doi: 10.1056/NEJMicm2204528.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36652357" target="_blank">36652357</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28779197">Intussusception: past, present and future.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Edwards EA,
|
||
Pigg N,
|
||
Courtier J,
|
||
Zapala MA,
|
||
MacKenzie JD,
|
||
Phelps AS</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
2017 Aug;47(9):1101-1108.
|
||
Epub 2017 Aug 4
|
||
doi: 10.1007/s00247-017-3878-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28779197" target="_blank">28779197</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27018962">Ileocecal Intussusception.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cook MA,
|
||
Shah J</span><br />
|
||
<span class="medgenPMjournal">J Am Osteopath Assoc</span>
|
||
2016 Apr;116(4):268.
|
||
doi: 10.7556/jaoa.2016.053.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27018962" target="_blank">27018962</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1422744">Paediatric intussusception.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Stringer MD,
|
||
Pablot SM,
|
||
Brereton RJ</span><br />
|
||
<span class="medgenPMjournal">Br J Surg</span>
|
||
1992 Sep;79(9):867-76.
|
||
doi: 10.1002/bjs.1800790906.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1422744" target="_blank">1422744</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7447689">Jejunogastric intussusception.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Waits JO,
|
||
Beart RW Jr,
|
||
Charboneau JW</span><br />
|
||
<span class="medgenPMjournal">Arch Surg</span>
|
||
1980 Dec;115(12):1449-52.
|
||
doi: 10.1001/archsurg.1980.01380120023006.
|
||
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<div class="nl"><a target="_blank" href="/pubmed/39201261">New Interpretations for Sprouting, Intussusception, Ansiform, and Coalescent Types of Angiogenesis.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/33158508">Management of intussusception in children: A systematic review.</a></div>
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</div>
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<div class="portlet mgSection" id="ID_104">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln">
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<div class="nl"><a target="_blank" href="/pubmed/34049735">Safety of vaccines used for routine immunization in the United States: An updated systematic review and meta-analysis.</a></div>
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<span class="bold">PMID: </span><a href="/pubmed/34049735" target="_blank">34049735</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/33970192">Association of Rotavirus Vaccines With Reduction in Rotavirus Gastroenteritis in Children Younger Than 5 Years: A Systematic Review and Meta-analysis of Randomized Clinical Trials and Observational Studies.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Sun ZW,
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Fu Y,
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Lu HL,
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Yang RX,
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Epub 2021 Jul 6
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<span class="bold">PMID: </span><a href="/pubmed/33970192" target="_blank">33970192</a><a href="/pmc/articles/PMC8111566" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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||
|
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<div class="nl"><a target="_blank" href="/pubmed/33158508">Management of intussusception in children: A systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Kelley-Quon LI,
|
||
Arthur LG,
|
||
Williams RF,
|
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Goldin AB,
|
||
St Peter SD,
|
||
Beres AL,
|
||
Hu YY,
|
||
Renaud EJ,
|
||
Ricca R,
|
||
Slidell MB,
|
||
Taylor A,
|
||
Smith CA,
|
||
Miniati D,
|
||
Sola JE,
|
||
Valusek P,
|
||
Berman L,
|
||
Raval MV,
|
||
Gosain A,
|
||
Dellinger MB,
|
||
Sømme S,
|
||
Downard CD,
|
||
McAteer JP,
|
||
Kawaguchi A</span><br />
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<span class="medgenPMjournal">J Pediatr Surg</span>
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2021 Mar;56(3):587-596.
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Epub 2020 Oct 6
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doi: 10.1016/j.jpedsurg.2020.09.055.
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<span class="bold">PMID: </span><a href="/pubmed/33158508" target="_blank">33158508</a><a href="/pmc/articles/PMC7920908" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/20581245">Peutz-Jeghers syndrome: a systematic review and recommendations for management.</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Intussusception%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 (68)</a></div></div>
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