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<!--
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UID=6816
|
||
ConceptID=C0019270
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Hernia</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>6816</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.">C0019270</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Hernias</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Hernia (414403008); Herniated structure (414403008); Herniated tissue (414403008); Herniation (414403008)</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:0100790">HP:0100790</a></td></tr>
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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>
|
||
<div class="portlet_content ln">The protrusion of part of an organ or fibroadipose tissue through an abnormal opening. [from <a title="NCI Thesaurus" href="http://ncit.nci.nih.gov" class="defSource" target="_blank">NCI</a>]</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">Hernia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/1763488" ref="tree=MeSH" title="MedGen record for Abnormality of the musculoskeletal system">Abnormality of the musculoskeletal system</a></span><ul><li><span class="TLline"><a href="/medgen/871127" ref="tree=MeSH" title="MedGen record for Abnormality of connective tissue">Abnormality of connective tissue</a></span><ul><li><span class="matched_ds">Hernia</span><ul><li><span class="TLline"><a href="/medgen/4934" ref="tree=MeSH" title="MedGen record for Cephalocele">Cephalocele</a></span><ul><li><span class="TLline"><a href="/medgen/332248" ref="tree=MeSH" title="MedGen record for Atretic occipital cephalocele">Atretic occipital cephalocele</a></span></li><li><span class="TLline"><a href="/medgen/1830107" ref="tree=MeSH" title="MedGen record for Isolated encephalocele">Isolated encephalocele</a></span><ul><li><span class="TLline"><a href="/medgen/868771" ref="tree=MeSH" title="MedGen record for Basal encephalocele">Basal encephalocele</a></span></li><li><span class="TLline"><a href="/medgen/98460" ref="tree=MeSH" title="MedGen record for Frontal encephalocele">Frontal encephalocele</a></span></li><li><span class="TLline"><a href="/medgen/507680" ref="tree=MeSH" title="MedGen record for Nasal encephalocele">Nasal encephalocele</a></span></li><li><span class="TLline"><a href="/medgen/4935" ref="tree=MeSH" title="MedGen record for Occipital encephalocele">Occipital encephalocele</a></span></li><li><span class="TLline"><a href="/medgen/488903" ref="tree=MeSH" title="MedGen record for Parietal encephalocele">Parietal encephalocele</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/82743" ref="tree=MeSH" title="MedGen record for Meningoencephalocele">Meningoencephalocele</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/68625" ref="tree=MeSH" title="MedGen record for Congenital diaphragmatic hernia">Congenital diaphragmatic hernia</a></span><ul><li><span class="TLline"><a href="/medgen/1369533" ref="tree=MeSH" title="MedGen record for Central diaphragmatic hernia">Central diaphragmatic hernia</a></span></li><li><span class="TLline"><a href="/medgen/327154" ref="tree=MeSH" title="MedGen record for Diaphragmatic hernia 1">Diaphragmatic hernia 1</a></span></li><li><span class="TLline"><a href="/medgen/347411" ref="tree=MeSH" title="MedGen record for Diaphragmatic hernia 2">Diaphragmatic hernia 2</a></span></li><li><span class="TLline"><a href="/medgen/347546" ref="tree=MeSH" title="MedGen record for Diaphragmatic hernia 3">Diaphragmatic hernia 3</a></span></li><li><span class="TLline"><a href="/medgen/334881" ref="tree=MeSH" title="MedGen record for Hernia, anterior diaphragmatic">Hernia, anterior diaphragmatic</a></span></li><li><span class="TLline"><a href="/medgen/539425" ref="tree=MeSH" title="MedGen record for Morgagni diaphragmatic hernia">Morgagni diaphragmatic hernia</a></span></li><li><span class="TLline"><a href="/medgen/539426" ref="tree=MeSH" title="MedGen record for Posterolateral diaphragmatic hernia">Posterolateral diaphragmatic hernia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/488957" ref="tree=MeSH" title="MedGen record for Congenital meningocele">Congenital meningocele</a></span><ul><li><span class="TLline"><a href="/medgen/507591" ref="tree=MeSH" title="MedGen record for Congenital cerebral meningocele">Congenital cerebral meningocele</a></span></li><li><span class="TLline"><a href="/medgen/507597" ref="tree=MeSH" title="MedGen record for Congenital spinal meningocele">Congenital spinal meningocele</a></span><ul><li><span class="TLline"><a href="/medgen/768674" ref="tree=MeSH" title="MedGen record for Cervical Meningocele">Cervical Meningocele</a></span></li><li><span class="TLline"><a href="/medgen/768675" ref="tree=MeSH" title="MedGen record for Lumbar Meningocele">Lumbar Meningocele</a></span></li><li><span class="TLline"><a href="/medgen/101069" ref="tree=MeSH" title="MedGen record for Sacral meningocele">Sacral meningocele</a></span></li><li><span class="TLline"><a href="/medgen/768676" ref="tree=MeSH" title="MedGen record for Thoracic Meningocele">Thoracic Meningocele</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/5530" ref="tree=MeSH" title="MedGen record for Diaphragmatic hernia">Diaphragmatic hernia</a></span><ul><li><span class="TLline"><a href="/medgen/483347" ref="tree=MeSH" title="MedGen record for Hiatus hernia">Hiatus hernia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/7125" ref="tree=MeSH" title="MedGen record for Displacement of intervertebral disc">Displacement of intervertebral disc</a></span></li><li><span class="TLline"><a href="/medgen/9231" ref="tree=MeSH" title="MedGen record for Femoral hernia">Femoral hernia</a></span></li><li><span class="TLline"><a href="/medgen/867577" ref="tree=MeSH" title="MedGen record for Genital hernia">Genital hernia</a></span><ul><li><span class="TLline"><a href="/medgen/22591" ref="tree=MeSH" title="MedGen record for Uterine prolapse">Uterine prolapse</a></span><ul><li><span class="TLline"><a href="/medgen/821251" ref="tree=MeSH" title="MedGen record for Postpartum Uterine Inversion">Postpartum Uterine Inversion</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/488974" ref="tree=MeSH" title="MedGen record for Vaginal hernia">Vaginal hernia</a></span><ul><li><span class="TLline"><a href="/medgen/730551" ref="tree=MeSH" title="MedGen record for Cystocele">Cystocele</a></span></li><li><span class="TLline"><a href="/medgen/57445" ref="tree=MeSH" title="MedGen record for Rectocele">Rectocele</a></span></li><li><span class="TLline"><a href="/medgen/451007" ref="tree=MeSH" title="MedGen record for Urethrocele">Urethrocele</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/488973" ref="tree=MeSH" title="MedGen record for Hernia of the abdominal wall">Hernia of the abdominal wall</a></span><ul><li><span class="TLline"><a href="/medgen/162756" ref="tree=MeSH" title="MedGen record for Congenital omphalocele">Congenital omphalocele</a></span><ul><li><span class="TLline"><a href="/medgen/478865" ref="tree=MeSH" title="MedGen record for Omphalocele, autosomal">Omphalocele, autosomal</a></span></li><li><span class="TLline"><a href="/medgen/477256" ref="tree=MeSH" title="MedGen record for Omphalocele, X-linked">Omphalocele, X-linked</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/488830" ref="tree=MeSH" title="MedGen record for Incisional hernia">Incisional hernia</a></span></li><li><span class="TLline"><a href="/medgen/6817" ref="tree=MeSH" title="MedGen record for Inguinal hernia">Inguinal hernia</a></span><ul><li><span class="TLline"><a href="/medgen/6818" ref="tree=MeSH" title="MedGen record for Direct inguinal hernia">Direct inguinal hernia</a></span></li><li><span class="TLline"><a href="/medgen/7082" ref="tree=MeSH" title="MedGen record for Inguinal Hernia without Mention of Obstruction or Gangrene">Inguinal Hernia without Mention of Obstruction or Gangrene</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/9232" ref="tree=MeSH" title="MedGen record for Umbilical hernia">Umbilical hernia</a></span><ul><li><span class="TLline"><a href="/medgen/510189" ref="tree=MeSH" title="MedGen record for Umbilical hernia with gangrene">Umbilical hernia with gangrene</a></span></li><li><span class="TLline"><a href="/medgen/237028" ref="tree=MeSH" title="MedGen record for Umbilical Hernia with Obstruction without Mention of Gangrene">Umbilical Hernia with Obstruction without Mention of Gangrene</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/5531" ref="tree=MeSH" title="MedGen record for Ventral hernia">Ventral hernia</a></span><ul><li><span class="TLline"><a href="/medgen/224929" ref="tree=MeSH" title="MedGen record for Exumbilication">Exumbilication</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/232604" ref="tree=MeSH" title="MedGen record for Hernia with Obstruction without Mention of Gangrene">Hernia with Obstruction without Mention of Gangrene</a></span><ul><li><span class="TLline"><a href="/medgen/234476" ref="tree=MeSH" title="MedGen record for Ventral Hernia with Obstruction without Mention of Gangrene">Ventral Hernia with Obstruction without Mention of Gangrene</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/5529" ref="tree=MeSH" title="MedGen record for Hernia without Mention of Obstruction or Gangrene">Hernia without Mention of Obstruction or Gangrene</a></span></li><li><span class="TLline"><a href="/medgen/1716807" ref="tree=MeSH" title="MedGen record for Hernia, Internal">Hernia, Internal</a></span><ul><li><span class="TLline"><a href="/medgen/1719957" ref="tree=MeSH" title="MedGen record for Paraduodenal Hernia">Paraduodenal Hernia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/59810" ref="tree=MeSH" title="MedGen record for Intra-abdominal hernia">Intra-abdominal hernia</a></span><ul><li><span class="TLline"><a href="/medgen/507789" ref="tree=MeSH" title="MedGen record for Epigastric hernia">Epigastric hernia</a></span></li><li><span class="TLline"><a href="/medgen/82721" ref="tree=MeSH" title="MedGen record for Gastroschisis">Gastroschisis</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</div>
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<div class="portlet mgSection" id="ID_112">
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<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">
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<div class="divPopper rprt" id="rdis_5288"><div><strong>Fucosidosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>5288</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.">C0016788</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Fucosidosis is an autosomal recessive lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues. Clinical features include angiokeratoma, progressive psychomotor retardation, neurologic signs, coarse facial features, and dysostosis multiplex. Fucosidosis has been classified into 2 major types. Type 1 is characterized by rapid psychomotor regression and severe neurologic deterioration beginning at about 6 months of age, elevated sweat sodium chloride, and death within the first decade of life. Type 2 is characterized by milder psychomotor retardation and neurologic signs, the development of angiokeratoma corporis diffusum, normal sweat salinity, and longer survival (Kousseff et al., 1976).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/5288">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_39477"><div><strong>Mucopolysaccharidosis, MPS-III-C</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>39477</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.">C0086649</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Mucopolysaccharidosis type III (MPS III) is a multisystem lysosomal storage disease characterized by progressive central nervous system degeneration manifest as severe intellectual disability (ID), developmental regression, and other neurologic manifestations including autism spectrum disorder (ASD), behavioral problems, and sleep disturbances. Disease onset is typically before age ten years. Disease course may be rapidly or slowly progressive; some individuals with an extremely attenuated disease course present in mid-to-late adulthood with early-onset dementia with or without a history of ID. Systemic manifestations can include musculoskeletal problems (joint stiffness, contractures, scoliosis, and hip dysplasia), hearing loss, respiratory tract and sinopulmonary infections, and cardiac disease (valvular thickening, defects in the cardiac conduction system). Neurologic decline is seen in all affected individuals; however, clinical severity varies within and among the four MPS III subtypes (defined by the enzyme involved) and even among members of the same family. Death usually occurs in the second or third decade of life secondary to neurologic regression or respiratory tract infections.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/39477">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_39698"><div><strong>Hurler syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>39698</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.">C0086795</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Mucopolysaccharidosis type I (MPS I) is a progressive multisystem disorder with features ranging over a continuum of severity. While affected individuals have traditionally been classified as having one of three MPS I syndromes (Hurler syndrome, Hurler-Scheie syndrome, or Scheie syndrome), no easily measurable biochemical differences have been identified and the clinical findings overlap. Affected individuals are best described as having either a phenotype consistent with either severe (Hurler syndrome) or attenuated MPS I, a distinction that influences therapeutic options. Severe MPS I: Infants appear normal at birth. Typical early manifestations are nonspecific (e.g., umbilical or inguinal hernia, frequent upper respiratory tract infections before age 1 year). Coarsening of the facial features may not become apparent until after age one year. Gibbus deformity of the lower spine is common and often noted within the first year. Progressive skeletal dysplasia (dysostosis multiplex) involving all bones is universal, as is progressive arthropathy involving most joints. By age three years, linear growth decreases. Intellectual disability is progressive and profound but may not be readily apparent in the first year of life. Progressive cardiorespiratory involvement, hearing loss, and corneal clouding are common. Without treatment, death (typically from cardiorespiratory failure) usually occurs within the first ten years of life. Attenuated MPS I: Clinical onset is usually between ages three and ten years. The severity and rate of disease progression range from serious life-threatening complications leading to death in the second to third decade, to a normal life span complicated by significant disability from progressive joint manifestations and cardiorespiratory disease. While some individuals have no neurologic involvement and psychomotor development may be normal in early childhood, learning disabilities and psychiatric manifestations can be present later in life. Hearing loss, cardiac valvular disease, respiratory involvement, and corneal clouding are common.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/39698">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_120516"><div><strong>Freeman-Sheldon syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>120516</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.">C0265224</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Freeman-Sheldon syndrome (FSS), or DA2A, is phenotypically similar to DA1. In addition to contractures of the hands and feet, FSS is characterized by oropharyngeal abnormalities, scoliosis, and a distinctive face that includes a very small oral orifice (often only a few millimeters in diameter at birth), puckered lips, and an H-shaped dimple of the chin; hence, FSS has been called 'whistling face syndrome.' The limb phenotypes of DA1 and FSS may be so similar that they can only be distinguished by the differences in facial morphology (summary by Bamshad et al., 2009). For a general phenotypic description and a discussion of genetic heterogeneity of distal arthrogryposis, see DA1 (108120).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/120516">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_78649"><div><strong>Aspartylglucosaminuria</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>78649</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.">C0268225</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Aspartylglucosaminuria is a lysosomal storage disorder characterized by developmental delay, intellectual disability, behavioral manifestations (hyperactivity in young children, anxiety and restlessness in adolescence, and apathy in adulthood), recurrent infections, musculoskeletal features, and characteristic craniofacial features (prominent supraorbital ridges, hypertelorism, periorbital fullness, short nose with broad nasal bridge, thick vermilion of the upper and lower lips, and macroglossia) that become more prominent with age. Additional neurologic manifestations can include seizures, poor balance and coordination, and progressive cerebral atrophy in adulthood. Macrocephaly is common. Musculoskeletal features include lordosis, scoliosis, and arthritis in adolescents and young adults; vertebral dysplasia and/or rib cage abnormalities; and progressive muscle wasting, joint contractures, bursitis, and osteoporosis in adulthood. Skin manifestations (facial seborrhea, rosacea, and angiofibromas), gastrointestinal manifestations, neutropenia, and thrombocytopenia occur in some individuals. The clinical manifestations of aspartylglucosaminuria worsen with age, and adults have progressive psychomotor decline.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/78649">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_120628"><div><strong>Ehlers-Danlos syndrome, classic type, 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>120628</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.">C0268336</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Classic Ehlers-Danlos syndrome (cEDS) is a heritable connective tissue disorder characterized by skin hyperextensibility, atrophic scarring, and generalized joint hypermobility (GJH). The skin is soft, velvety, or doughy to the touch. In addition, the skin is hyperextensible, meaning that it extends easily and snaps back after release. The skin is fragile, as manifested by splitting of the dermis following relatively minor trauma, especially over pressure points (knees, elbows) and areas prone to trauma (shins, forehead, chin). Wound healing is poor, and stretching, thinning, and pigmentation of scars is characteristic, leading to the presence of atrophic and/or hemosiderotic scars. Easy bruising is also a hallmark of cEDS. GJH is present in most but not all affected individuals, evidenced by the presence of a Beighton score of five or greater, either on examination or historically. Joint instability complications may comprise sprains and dislocations/subluxations. Mild muscle hypotonia with delayed motor development, fatigue and muscle cramps, and some skeletal morphologic alterations (scoliosis, pectus deformities, genus/hallux valgus, pes planus) are regularly observed. While aortic root dilatation and mitral valve prolapse are seen in cEDS, they are rarely clinically significant. Arterial aneurysm and rupture have been reported in a few individuals with cEDS.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/120628">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_163225"><div><strong>Toriello-Carey syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>163225</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.">C0796184</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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||
<div class="spaceAbove">Toriello-Carey syndrome is a multiple congenital anomaly disorder with variable systemic manifestations, most commonly including mental retardation, agenesis of the corpus callosum, postnatal growth delay, cardiac defects, usually septal defects, distal limb defects, and urogenital anomalies in affected males. Patients have facial dysmorphic features, micrognathia, including full cheeks, hypertelorism, flattened nasal bridge, anteverted nares, and short neck. Not all features are found in all patients and some patients may have additional features such as anal anomalies or hernias (summary by Toriello et al., 2003). In a review of the Toriello-Carey syndrome, Toriello et al. (2016) stated that while corpus callosum abnormalities and micrognathia with highly arched or cleft palate are seen in most patients, other manifestations are widely variable. They noted that etiologic heterogeneity has been observed in reported patients, with at least 20% of patients having chromosome anomalies, and that no good candidate genes have been identified by exome sequencing. The authors commented that this condition might not be a unitary diagnostic entity. They recommended chromosome microarray for any child suspected of having the condition, followed by standard of care by genetic testing.</div>
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||
<div class="spaceAbove nowrap">See: <a href="/medgen/163225">Condition Record</a></div></div>
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||
<div class="divPopper rprt" id="rdis_355421"><div><strong>Megalencephaly-capillary malformation-polymicrogyria syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>355421</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.">C1865285</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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||
<div class="spaceAbove">PIK3CA-related overgrowth spectrum (PROS) encompasses a range of clinical findings in which the core features are congenital or early-childhood onset of segmental/focal overgrowth with or without cellular dysplasia. Prior to the identification of PIK3CA as the causative gene, PROS was separated into distinct clinical syndromes based on the tissues and/or organs involved (e.g., MCAP [megalencephaly-capillary malformation] syndrome and CLOVES [congenital lipomatous asymmetric overgrowth of the trunk, lymphatic, capillary, venous, and combined-type vascular malformations, epidermal nevi, skeletal and spinal anomalies] syndrome). The predominant areas of overgrowth include the brain, limbs (including fingers and toes), trunk (including abdomen and chest), and face, all usually in an asymmetric distribution. Generalized brain overgrowth may be accompanied by secondary overgrowth of specific brain structures resulting in ventriculomegaly, a markedly thick corpus callosum, and cerebellar tonsillar ectopia with crowding of the posterior fossa. Vascular malformations may include capillary, venous, and less frequently, arterial or mixed (capillary-lymphatic-venous or arteriovenous) malformations. Lymphatic malformations may be in various locations (internal and/or external) and can cause various clinical issues, including swelling, pain, and occasionally localized bleeding secondary to trauma. Lipomatous overgrowth may occur ipsilateral or contralateral to a vascular malformation, if present. The degree of intellectual disability appears to be mostly related to the presence and severity of seizures, cortical dysplasia (e.g., polymicrogyria), and hydrocephalus. Many children have feeding difficulties that are often multifactorial in nature. Endocrine issues affect a small number of individuals and most commonly include hypoglycemia (largely hypoinsulinemic hypoketotic hypoglycemia), hypothyroidism, and growth hormone deficiency.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/355421">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_899774"><div><strong>Cutis laxa, autosomal dominant 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>899774</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.">C4225268</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Autosomal dominant cutis laxa-3 (ADCL3) is characterized by thin skin with visible veins and wrinkles, cataract or corneal clouding, clenched fingers, pre- and postnatal growth retardation, and moderate intellectual disability. In addition, patients exhibit a combination of muscular hypotonia with brisk muscle reflexes (Fischer-Zirnsak et al., 2015). For a general phenotypic description and discussion of genetic heterogeneity of autosomal dominant cutis laxa, see ARCL1 (123700).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/899774">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_934711"><div><strong>Bone marrow failure syndrome 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934711</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.">C4310744</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Bone marrow failure syndrome-3 is an autosomal recessive disorder characterized by onset of pancytopenia in early childhood. Patients may have additional variable nonspecific somatic abnormalities, including poor growth, microcephaly, and skin anomalies (summary by Tummala et al., 2016). BMFS3 has a distinct phenotype and may include features that overlap with Shwachman-Diamond syndrome (SDS1; 260400), such as pancreatic insufficiency and short stature, and with dyskeratosis congenita (see, e.g., DKCA1, 127550), such as dental and hair abnormalities and shortened telomeres. In addition, some patients may have joint and skeletal abnormalities, impaired development, and retinal dysplasia (summary by D'Amours et al., 2018). For a discussion of genetic heterogeneity of BMFS, see BMFS1 (614675).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/934711">Condition Record</a></div></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_78649" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Aspartylglucosaminuria</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934711" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Bone marrow failure syndrome 3</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_899774" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cutis laxa, autosomal dominant 3</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_120628" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ehlers-Danlos syndrome, classic type, 2</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_120516" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Freeman-Sheldon syndrome</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (10)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_5288" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Fucosidosis</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_39698" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hurler syndrome</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_355421" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Megalencephaly-capillary malformation-polymicrogyria syndrome</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_39477" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucopolysaccharidosis, MPS-III-C</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_163225" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Toriello-Carey syndrome</a></div></span></div></div>
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</div>
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<div class="portlet mgSection" id="ID_105">
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<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>
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<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>
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<div class="nl"><a target="_blank" href="/pubmed/35123084">AGA Clinical Practice Update on the Personalized Approach to the Evaluation and Management of GERD: Expert Review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Yadlapati R,
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Gyawali CP,
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Pandolfino JE;
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CGIT GERD Consensus Conference Participants</span><br />
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<span class="medgenPMjournal">Clin Gastroenterol Hepatol</span>
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2022 May;20(5):984-994.e1.
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Epub 2022 Feb 2
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doi: 10.1016/j.cgh.2022.01.025.
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<span class="bold">PMID: </span><a href="/pubmed/35123084" target="_blank">35123084</a><a href="/pmc/articles/PMC9838103" 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/33064426">Inguinal Hernias: Diagnosis and Management.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Shakil A,
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Aparicio K,
|
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Barta E,
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Munez K</span><br />
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<span class="medgenPMjournal">Am Fam Physician</span>
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2020 Oct 15;102(8):487-492.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33064426" target="_blank">33064426</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29330835">International guidelines for groin hernia management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">HerniaSurge Group</span><br />
|
||
<span class="medgenPMjournal">Hernia</span>
|
||
2018 Feb;22(1):1-165.
|
||
Epub 2018 Jan 12
|
||
doi: 10.1007/s10029-017-1668-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29330835" target="_blank">29330835</a><a href="/pmc/articles/PMC5809582" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22hernia%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 (1160)</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/37709390">Hernia Formation: Risk Factors and Biology.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Haskins IN</span><br />
|
||
<span class="medgenPMjournal">Surg Clin North Am</span>
|
||
2023 Oct;103(5):835-846.
|
||
Epub 2023 Jun 2
|
||
doi: 10.1016/j.suc.2023.04.020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37709390" target="_blank">37709390</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35259338">Inguinal Hernia Repair in Older Persons.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Perez AJ,
|
||
Campbell S</span><br />
|
||
<span class="medgenPMjournal">J Am Med Dir Assoc</span>
|
||
2022 Apr;23(4):563-567.
|
||
Epub 2022 Mar 5
|
||
doi: 10.1016/j.jamda.2022.02.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35259338" target="_blank">35259338</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32828548">Paraesophageal hernia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lin ZS,
|
||
Chen XJ,
|
||
Jin Z</span><br />
|
||
<span class="medgenPMjournal">Med Clin (Barc)</span>
|
||
2021 Aug 13;157(3):157.
|
||
Epub 2020 Aug 20
|
||
doi: 10.1016/j.medcli.2020.06.049.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32828548" target="_blank">32828548</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18267160">Pediatric hernias.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Brandt ML</span><br />
|
||
<span class="medgenPMjournal">Surg Clin North Am</span>
|
||
2008 Feb;88(1):27-43, vii-viii.
|
||
doi: 10.1016/j.suc.2007.11.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18267160" target="_blank">18267160</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8803572">Hiatal hernia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Johnson DA,
|
||
Ruffin WK</span><br />
|
||
<span class="medgenPMjournal">Gastrointest Endosc Clin N Am</span>
|
||
1996 Jul;6(3):641-66.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8803572" target="_blank">8803572</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hernia%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 (21302)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37709394">Management of Chronic Postoperative Inguinal Pain.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Krpata DM</span><br />
|
||
<span class="medgenPMjournal">Surg Clin North Am</span>
|
||
2023 Oct;103(5):889-900.
|
||
Epub 2023 May 11
|
||
doi: 10.1016/j.suc.2023.04.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37709394" target="_blank">37709394</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36610072">Hiatal hernia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Musbahi A,
|
||
Mahawar K</span><br />
|
||
<span class="medgenPMjournal">Br J Surg</span>
|
||
2023 Mar 30;110(4):401-402.
|
||
doi: 10.1093/bjs/znac449.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36610072" target="_blank">36610072</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33064435">Inguinal (Groin) Hernias.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">Am Fam Physician</span>
|
||
2020 Oct 15;102(8):Online.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33064435" target="_blank">33064435</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28828685">Modern diagnosis and treatment of hiatal hernias.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Siegal SR,
|
||
Dolan JP,
|
||
Hunter JG</span><br />
|
||
<span class="medgenPMjournal">Langenbecks Arch Surg</span>
|
||
2017 Dec;402(8):1145-1151.
|
||
Epub 2017 Aug 21
|
||
doi: 10.1007/s00423-017-1606-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28828685" target="_blank">28828685</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8803572">Hiatal hernia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Johnson DA,
|
||
Ruffin WK</span><br />
|
||
<span class="medgenPMjournal">Gastrointest Endosc Clin N Am</span>
|
||
1996 Jul;6(3):641-66.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8803572" target="_blank">8803572</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hernia%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 (15585)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36456433">Prenatal management of congenital diaphragmatic hernia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Danzer E,
|
||
Rintoul NE,
|
||
van Meurs KP,
|
||
Deprest J</span><br />
|
||
<span class="medgenPMjournal">Semin Fetal Neonatal Med</span>
|
||
2022 Dec;27(6):101406.
|
||
Epub 2022 Nov 17
|
||
doi: 10.1016/j.siny.2022.101406.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36456433" target="_blank">36456433</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35286471">Open versus laparoscopic repair of inguinal hernia: an overview of systematic reviews of randomised controlled trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Haladu N,
|
||
Alabi A,
|
||
Brazzelli M,
|
||
Imamura M,
|
||
Ahmed I,
|
||
Ramsay G,
|
||
Scott NW</span><br />
|
||
<span class="medgenPMjournal">Surg Endosc</span>
|
||
2022 Jul;36(7):4685-4700.
|
||
Epub 2022 Mar 14
|
||
doi: 10.1007/s00464-022-09161-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35286471" target="_blank">35286471</a><a href="/pmc/articles/PMC9160137" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33839749">Identifying predictors of ventral hernia recurrence: systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Parker SG,
|
||
Mallett S,
|
||
Quinn L,
|
||
Wood CPJ,
|
||
Boulton RW,
|
||
Jamshaid S,
|
||
Erotocritou M,
|
||
Gowda S,
|
||
Collier W,
|
||
Plumb AAO,
|
||
Windsor ACJ,
|
||
Archer L,
|
||
Halligan S</span><br />
|
||
<span class="medgenPMjournal">BJS Open</span>
|
||
2021 Mar 5;5(2)
|
||
doi: 10.1093/bjsopen/zraa071.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33839749" target="_blank">33839749</a><a href="/pmc/articles/PMC8038271" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33427757">Treatment of Inguinal Hernia: Systematic Review and Updated Network Meta-analysis of Randomized Controlled Trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aiolfi A,
|
||
Cavalli M,
|
||
Ferraro SD,
|
||
Manfredini L,
|
||
Bonitta G,
|
||
Bruni PG,
|
||
Bona D,
|
||
Campanelli G</span><br />
|
||
<span class="medgenPMjournal">Ann Surg</span>
|
||
2021 Dec 1;274(6):954-961.
|
||
doi: 10.1097/SLA.0000000000004735.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33427757" target="_blank">33427757</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9057744">Laparoscopic surgery.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Johnson A</span><br />
|
||
<span class="medgenPMjournal">Lancet</span>
|
||
1997 Mar 1;349(9052):631-5.
|
||
doi: 10.1016/S0140-6736(96)10032-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9057744" target="_blank">9057744</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hernia%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (13596)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35546520">Port-site hernias in patients undergoing laparoscopic and/or robotic surgery: Can they be prevented?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Richards Y</span><br />
|
||
<span class="medgenPMjournal">J Perioper Pract</span>
|
||
2023 Sep;33(9):269-275.
|
||
Epub 2022 May 12
|
||
doi: 10.1177/17504589221094135.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35546520" target="_blank">35546520</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32200405">Major abdominal wall defects in the low- and middle-income setting: current status and priorities.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Anyanwu LC,
|
||
Ade-Ajayi N,
|
||
Rolle U</span><br />
|
||
<span class="medgenPMjournal">Pediatr Surg Int</span>
|
||
2020 May;36(5):579-590.
|
||
Epub 2020 Mar 21
|
||
doi: 10.1007/s00383-020-04638-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32200405" target="_blank">32200405</a><a href="/pmc/articles/PMC7165143" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30454419">Characterization of Pediatric Traumatic Diaphragm Injury.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Johnson MC,
|
||
Eastridge BJ,
|
||
Liao L</span><br />
|
||
<span class="medgenPMjournal">Am Surg</span>
|
||
2018 Mar 1;84(3):e91-e93.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30454419" target="_blank">30454419</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7878532">Surgery for adult polycystic liver disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Soravia C,
|
||
Mentha G,
|
||
Giostra E,
|
||
Morel P,
|
||
Rohner A</span><br />
|
||
<span class="medgenPMjournal">Surgery</span>
|
||
1995 Mar;117(3):272-5.
|
||
doi: 10.1016/s0039-6060(05)80201-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7878532" target="_blank">7878532</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8062027">Congenital diaphragmatic hernia: an unsolved problem.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harrison MR,
|
||
Adzick NS,
|
||
Flake AW</span><br />
|
||
<span class="medgenPMjournal">Semin Pediatr Surg</span>
|
||
1993 May;2(2):109-12.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8062027" target="_blank">8062027</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hernia%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 (10445)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/33961884">Double Heart-Shaped Silhouette.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ono R,
|
||
Kitagawa I</span><br />
|
||
<span class="medgenPMjournal">Gastroenterology</span>
|
||
2021 Aug;161(2):427-428.
|
||
Epub 2021 May 5
|
||
doi: 10.1053/j.gastro.2021.04.072.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33961884" target="_blank">33961884</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33609505">A Man With Two Gastric Bulbs.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chiang HC,
|
||
Kang JW,
|
||
Lin XZ</span><br />
|
||
<span class="medgenPMjournal">Gastroenterology</span>
|
||
2021 Sep;161(3):e12-e13.
|
||
Epub 2021 Feb 18
|
||
doi: 10.1053/j.gastro.2021.02.038.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33609505" target="_blank">33609505</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32725328">Perioperative and midterm outcomes of emergent robotic repair of incarcerated ventral and incisional hernia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kudsi OY,
|
||
Bou-Ayash N,
|
||
Chang K,
|
||
Gokcal F</span><br />
|
||
<span class="medgenPMjournal">J Robot Surg</span>
|
||
2021 Jun;15(3):473-481.
|
||
Epub 2020 Jul 28
|
||
doi: 10.1007/s11701-020-01130-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32725328" target="_blank">32725328</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31335403">Update on Congenital Diaphragmatic Hernia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chatterjee D,
|
||
Ing RJ,
|
||
Gien J</span><br />
|
||
<span class="medgenPMjournal">Anesth Analg</span>
|
||
2020 Sep;131(3):808-821.
|
||
doi: 10.1213/ANE.0000000000004324.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31335403" target="_blank">31335403</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23268122">MRI findings in fetuses with an abdominal wall defect: gastroschisis, omphalocele, and cloacal exstrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nakagawa M,
|
||
Hara M,
|
||
Shibamoto Y</span><br />
|
||
<span class="medgenPMjournal">Jpn J Radiol</span>
|
||
2013 Mar;31(3):153-9.
|
||
Epub 2012 Dec 26
|
||
doi: 10.1007/s11604-012-0163-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23268122" target="_blank">23268122</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hernia%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 (9350)</a></div></div>
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|
||
<div class="nl"><a target="_blank" href="/pubmed/36026550">Updated guideline for closure of abdominal wall incisions from the European and American Hernia Societies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Deerenberg EB,
|
||
Henriksen NA,
|
||
Antoniou GA,
|
||
Antoniou SA,
|
||
Bramer WM,
|
||
Fischer JP,
|
||
Fortelny RH,
|
||
Gök H,
|
||
Harris HW,
|
||
Hope W,
|
||
Horne CM,
|
||
Jensen TK,
|
||
Köckerling F,
|
||
Kretschmer A,
|
||
López-Cano M,
|
||
Malcher F,
|
||
Shao JM,
|
||
Slieker JC,
|
||
de Smet GHJ,
|
||
Stabilini C,
|
||
Torkington J,
|
||
Muysoms FE</span><br />
|
||
<span class="medgenPMjournal">Br J Surg</span>
|
||
2022 Nov 22;109(12):1239-1250.
|
||
doi: 10.1093/bjs/znac302.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36026550" target="_blank">36026550</a><a href="/pmc/articles/PMC10364727" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34609697">Robotic versus laparoscopic inguinal hernia repair: an updated systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Solaini L,
|
||
Cavaliere D,
|
||
Avanzolini A,
|
||
Rocco G,
|
||
Ercolani G</span><br />
|
||
<span class="medgenPMjournal">J Robot Surg</span>
|
||
2022 Aug;16(4):775-781.
|
||
Epub 2021 Oct 5
|
||
doi: 10.1007/s11701-021-01312-6.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34609697" target="_blank">34609697</a><a href="/pmc/articles/PMC9314304" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34546475">A systematic review and meta-analysis of technical aspects and clinical outcomes of botulinum toxin prior to abdominal wall reconstruction.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Timmer AS,
|
||
Claessen JJM,
|
||
Atema JJ,
|
||
Rutten MVH,
|
||
Hompes R,
|
||
Boermeester MA</span><br />
|
||
<span class="medgenPMjournal">Hernia</span>
|
||
2021 Dec;25(6):1413-1425.
|
||
Epub 2021 Sep 21
|
||
doi: 10.1007/s10029-021-02499-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34546475" target="_blank">34546475</a><a href="/pmc/articles/PMC8613151" 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/33839749">Identifying predictors of ventral hernia recurrence: systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Parker SG,
|
||
Mallett S,
|
||
Quinn L,
|
||
Wood CPJ,
|
||
Boulton RW,
|
||
Jamshaid S,
|
||
Erotocritou M,
|
||
Gowda S,
|
||
Collier W,
|
||
Plumb AAO,
|
||
Windsor ACJ,
|
||
Archer L,
|
||
Halligan S</span><br />
|
||
<span class="medgenPMjournal">BJS Open</span>
|
||
2021 Mar 5;5(2)
|
||
doi: 10.1093/bjsopen/zraa071.
|
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<span class="bold">PMID: </span><a href="/pubmed/33839749" target="_blank">33839749</a><a href="/pmc/articles/PMC8038271" 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/33427757">Treatment of Inguinal Hernia: Systematic Review and Updated Network Meta-analysis of Randomized Controlled Trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aiolfi A,
|
||
Cavalli M,
|
||
Ferraro SD,
|
||
Manfredini L,
|
||
Bonitta G,
|
||
Bruni PG,
|
||
Bona D,
|
||
Campanelli G</span><br />
|
||
<span class="medgenPMjournal">Ann Surg</span>
|
||
2021 Dec 1;274(6):954-961.
|
||
doi: 10.1097/SLA.0000000000004735.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33427757" target="_blank">33427757</a></div>
|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hernia%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 (1083)</a></div></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22hernia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Hernia%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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