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<!--
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||
UID=105507
|
||
ConceptID=C0522055
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Abnormal EKG</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>105507</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.">C0522055</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Abnormal ECG; Abnormal electrocardiogram; ECG abnormalities; EKG abnormalities; Electrocardiographic abnormalities</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Abnormal EKG finding (102594003); Abnormal ECG (102594003); Electrocardiogram abnormal (102594003)</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:0003115">HP:0003115</a></td></tr>
|
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</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>
|
||
<div class="portlet_content ln">Abnormal rhythm of the heart. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Abnormal EKG</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/1715859" ref="tree=MeSH" title="MedGen record for Abnormal Cardiac Study">Abnormal Cardiac Study</a></span><ul><li><span class="matched_ds">Abnormal EKG</span><ul><li><span class="TLline"><a href="/medgen/1638207" ref="tree=MeSH" title="MedGen record for Abnormal P wave">Abnormal P wave</a></span><ul><li><span class="TLline"><a href="/medgen/324892" ref="tree=MeSH" title="MedGen record for Absent P wave">Absent P wave</a></span></li><li><span class="TLline"><a href="/medgen/455867" ref="tree=MeSH" title="MedGen record for Notched P wave">Notched P wave</a></span></li><li><span class="TLline"><a href="/medgen/68560" ref="tree=MeSH" title="MedGen record for P mitrale">P mitrale</a></span></li><li><span class="TLline"><a href="/medgen/66673" ref="tree=MeSH" title="MedGen record for P pulmonale">P pulmonale</a></span></li><li><span class="TLline"><a href="/medgen/1646973" ref="tree=MeSH" title="MedGen record for P wave inversion">P wave inversion</a></span></li><li><span class="TLline"><a href="/medgen/606917" ref="tree=MeSH" title="MedGen record for Prolonged P wave">Prolonged P wave</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1634800" ref="tree=MeSH" title="MedGen record for Abnormal PR interval">Abnormal PR interval</a></span><ul><li><span class="TLline"><a href="/medgen/154645" ref="tree=MeSH" title="MedGen record for Prolonged PR interval">Prolonged PR interval</a></span></li><li><span class="TLline"><a href="/medgen/105466" ref="tree=MeSH" title="MedGen record for Shortened PR interval">Shortened PR interval</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1631502" ref="tree=MeSH" title="MedGen record for Abnormal PR segment">Abnormal PR segment</a></span><ul><li><span class="TLline"><a href="/medgen/1647462" ref="tree=MeSH" title="MedGen record for PR segment depression">PR segment depression</a></span></li><li><span class="TLline"><a href="/medgen/1630951" ref="tree=MeSH" title="MedGen record for PR segment elevation">PR segment elevation</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1370423" ref="tree=MeSH" title="MedGen record for Abnormal QRS complex">Abnormal QRS complex</a></span><ul><li><span class="TLline"><a href="/medgen/1368676" ref="tree=MeSH" title="MedGen record for Abnormal QRS voltage">Abnormal QRS voltage</a></span><ul><li><span class="TLline"><a href="/medgen/811047" ref="tree=MeSH" title="MedGen record for Decreased QRS voltage">Decreased QRS voltage</a></span></li><li><span class="TLline"><a href="/medgen/215131" ref="tree=MeSH" title="MedGen record for Electrical alternans">Electrical alternans</a></span></li><li><span class="TLline"><a href="/medgen/909971" ref="tree=MeSH" title="MedGen record for Increased QRS voltage">Increased QRS voltage</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/489828" ref="tree=MeSH" title="MedGen record for Prolonged QRS complex">Prolonged QRS complex</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1620328" ref="tree=MeSH" title="MedGen record for Abnormal QT interval">Abnormal QT interval</a></span><ul><li><span class="TLline"><a href="/medgen/57494" ref="tree=MeSH" title="MedGen record for Prolonged QT interval">Prolonged QT interval</a></span><ul><li><span class="TLline"><a href="/medgen/167789" ref="tree=MeSH" title="MedGen record for Corrected Prolonged QT Interval by ECG Finding">Corrected Prolonged QT Interval by ECG Finding</a></span></li><li><span class="TLline"><a href="/medgen/294666" ref="tree=MeSH" title="MedGen record for Prolonged QTc interval">Prolonged QTc interval</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/489827" ref="tree=MeSH" title="MedGen record for Shortened QT interval">Shortened QT interval</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1055241" ref="tree=MeSH" title="MedGen record for Abnormal R wave">Abnormal R wave</a></span><ul><li><span class="TLline"><a href="/medgen/1056261" ref="tree=MeSH" title="MedGen record for Poor R-wave progression">Poor R-wave progression</a></span></li><li><span class="TLline"><a href="/medgen/1056537" ref="tree=MeSH" title="MedGen record for Prominent V1-V2 R wave">Prominent V1-V2 R wave</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/868594" ref="tree=MeSH" title="MedGen record for Abnormal ST segment">Abnormal ST segment</a></span><ul><li><span class="TLline"><a href="/medgen/1701995" ref="tree=MeSH" title="MedGen record for Abnormal S wave">Abnormal S wave</a></span><ul><li><span class="TLline"><a href="/medgen/1690398" ref="tree=MeSH" title="MedGen record for Deep S wave in lead V5">Deep S wave in lead V5</a></span></li><li><span class="TLline"><a href="/medgen/1691411" ref="tree=MeSH" title="MedGen record for Prominent S wave in lead I">Prominent S wave in lead I</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/141712" ref="tree=MeSH" title="MedGen record for ST segment depression">ST segment depression</a></span></li><li><span class="TLline"><a href="/medgen/99256" ref="tree=MeSH" title="MedGen record for ST segment elevation">ST segment elevation</a></span><ul><li><span class="TLline"><a href="/medgen/1053145" ref="tree=MeSH" title="MedGen record for Coved type ST segment elevation">Coved type ST segment elevation</a></span></li><li><span class="TLline"><a href="/medgen/1054669" ref="tree=MeSH" title="MedGen record for Saddle-back type ST segment elevation">Saddle-back type ST segment elevation</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/326862" ref="tree=MeSH" title="MedGen record for Abnormal T-wave">Abnormal T-wave</a></span><ul><li><span class="TLline"><a href="/medgen/416962" ref="tree=MeSH" title="MedGen record for Notched T wave">Notched T wave</a></span></li><li><span class="TLline"><a href="/medgen/65981" ref="tree=MeSH" title="MedGen record for T Wave Peaked by ECG Finding">T Wave Peaked by ECG Finding</a></span></li><li><span class="TLline"><a href="/medgen/418085" ref="tree=MeSH" title="MedGen record for T Waves Biphasic by ECG Finding">T Waves Biphasic by ECG Finding</a></span></li><li><span class="TLline"><a href="/medgen/418086" ref="tree=MeSH" title="MedGen record for T Waves Flat by ECG Finding">T Waves Flat by ECG Finding</a></span></li><li><span class="TLline"><a href="/medgen/745313" ref="tree=MeSH" title="MedGen record for T-wave alternans">T-wave alternans</a></span></li><li><span class="TLline"><a href="/medgen/105467" ref="tree=MeSH" title="MedGen record for T-wave inversion">T-wave inversion</a></span><ul><li><span class="TLline"><a href="/medgen/871172" ref="tree=MeSH" title="MedGen record for T-wave inversion in the right precordial leads">T-wave inversion in the right precordial leads</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/820422" ref="tree=MeSH" title="MedGen record for Abnormal U wave">Abnormal U wave</a></span><ul><li><span class="TLline"><a href="/medgen/369497" ref="tree=MeSH" title="MedGen record for Prominent U wave">Prominent U wave</a></span></li><li><span class="TLline"><a href="/medgen/1370051" ref="tree=MeSH" title="MedGen record for U wave inversion">U wave inversion</a></span><ul><li><span class="TLline"><a href="/medgen/1369196" ref="tree=MeSH" title="MedGen record for Exercise-induced U wave inversion">Exercise-induced U wave inversion</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/1785810" ref="tree=MeSH" title="MedGen record for Abnormal ventricular axis">Abnormal ventricular axis</a></span><ul><li><span class="TLline"><a href="/medgen/1781817" ref="tree=MeSH" title="MedGen record for Extreme axis deviation">Extreme axis deviation</a></span></li><li><span class="TLline"><a href="/medgen/1786835" ref="tree=MeSH" title="MedGen record for Indeterminate ventricular axis">Indeterminate ventricular axis</a></span></li><li><span class="TLline"><a href="/medgen/534423" ref="tree=MeSH" title="MedGen record for Left axis deviation">Left axis deviation</a></span></li><li><span class="TLline"><a href="/medgen/534422" ref="tree=MeSH" title="MedGen record for Right axis deviation">Right axis deviation</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1815063" ref="tree=MeSH" title="MedGen record for Epsilon wave">Epsilon wave</a></span></li><li><span class="TLline"><a href="/medgen/1053344" ref="tree=MeSH" title="MedGen record for Irregular P-P interval">Irregular P-P interval</a></span></li><li><span class="TLline"><a href="/medgen/1054485" ref="tree=MeSH" title="MedGen record for Irregular RR interval">Irregular RR interval</a></span></li><li><span class="TLline"><a href="/medgen/866319" ref="tree=MeSH" title="MedGen record for J wave">J wave</a></span></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_3925"><div><strong>Duchenne muscular dystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>3925</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.">C0013264</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">The dystrophinopathies cover a spectrum of X-linked muscle disease ranging from mild to severe that includes Duchenne muscular dystrophy, Becker muscular dystrophy, and DMD-associated dilated cardiomyopathy (DCM). The mild end of the spectrum includes the phenotypes of asymptomatic increase in serum concentration of creatine phosphokinase (CK) and muscle cramps with myoglobinuria. The severe end of the spectrum includes progressive muscle diseases that are classified as Duchenne/Becker muscular dystrophy when skeletal muscle is primarily affected and as DMD-associated DCM when the heart is primarily affected. Duchenne muscular dystrophy (DMD) usually presents in early childhood with delayed motor milestones including delays in walking independently and standing up from a supine position. Proximal weakness causes a waddling gait and difficulty climbing stairs, running, jumping, and standing up from a squatting position. DMD is rapidly progressive, with affected children being wheelchair dependent by age 12 years. Cardiomyopathy occurs in almost all individuals with DMD after age 18 years. Few survive beyond the third decade, with respiratory complications and progressive cardiomyopathy being common causes of death. Becker muscular dystrophy (BMD) is characterized by later-onset skeletal muscle weakness. With improved diagnostic techniques, it has been recognized that the mild end of the spectrum includes men with onset of symptoms after age 30 years who remain ambulatory even into their 60s. Despite the milder skeletal muscle involvement, heart failure from DCM is a common cause of morbidity and the most common cause of death in BMD. Mean age of death is in the mid-40s. DMD-associated DCM is characterized by left ventricular dilatation and congestive heart failure. Females heterozygous for a DMD pathogenic variant are at increased risk for DCM.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/3925">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_182959"><div><strong>Becker muscular dystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>182959</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.">C0917713</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">The dystrophinopathies cover a spectrum of X-linked muscle disease ranging from mild to severe that includes Duchenne muscular dystrophy, Becker muscular dystrophy, and DMD-associated dilated cardiomyopathy (DCM). The mild end of the spectrum includes the phenotypes of asymptomatic increase in serum concentration of creatine phosphokinase (CK) and muscle cramps with myoglobinuria. The severe end of the spectrum includes progressive muscle diseases that are classified as Duchenne/Becker muscular dystrophy when skeletal muscle is primarily affected and as DMD-associated DCM when the heart is primarily affected. Duchenne muscular dystrophy (DMD) usually presents in early childhood with delayed motor milestones including delays in walking independently and standing up from a supine position. Proximal weakness causes a waddling gait and difficulty climbing stairs, running, jumping, and standing up from a squatting position. DMD is rapidly progressive, with affected children being wheelchair dependent by age 12 years. Cardiomyopathy occurs in almost all individuals with DMD after age 18 years. Few survive beyond the third decade, with respiratory complications and progressive cardiomyopathy being common causes of death. Becker muscular dystrophy (BMD) is characterized by later-onset skeletal muscle weakness. With improved diagnostic techniques, it has been recognized that the mild end of the spectrum includes men with onset of symptoms after age 30 years who remain ambulatory even into their 60s. Despite the milder skeletal muscle involvement, heart failure from DCM is a common cause of morbidity and the most common cause of death in BMD. Mean age of death is in the mid-40s. DMD-associated DCM is characterized by left ventricular dilatation and congestive heart failure. Females heterozygous for a DMD pathogenic variant are at increased risk for DCM.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/182959">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_254845"><div><strong>Muscular dystrophy, cardiac type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>254845</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.">C1442927</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/254845">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_331805"><div><strong>Bethlem myopathy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>331805</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.">C1834674</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Bethlem myopathy-1 (BTHLM1) is a congenital muscular dystrophy characterized by distal joint laxity and a combination of distal and proximal joint contractures. The age at onset is highly variable, ranging from infancy to adulthood. Disease progression is slow and ambulation is usually retained into adulthood (summary by Butterfield et al., 2013). Genetic Heterogeneity of Bethlem Myopathy See Bethlem myopathy-1B (BTHLM1B; 620725), caused by mutation in the COL6A2 gene (120240) on chromosome 21q22; Bethlem myopathy-1C (620726), caused by mutation the COL6A3 gene (120250) on chromosome 2q37; and Bethlem myopathy-2 (BTHLM2; 616471), caused by mutation in the COL12A1 gene (120320) on chromosome 6q13-q14.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/331805">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_338087"><div><strong>Nathalie syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>338087</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.">C1850626</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Nathalie syndrome has characteristics of deafness, cataract, muscular atrophy, skeletal abnormalities, growth retardation, underdeveloped secondary sexual characteristics and electrocardiographic abnormalities. It has been described in a Dutch family: in three sisters (one named Nathalie) and their brother.</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/338087">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_383962"><div><strong>Friedreich ataxia 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>383962</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.">C1856689</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Typical Friedreich ataxia (FRDA) is characterized by progressive ataxia with onset from early childhood to early adulthood with mean age at onset from 10 to 15 years (range: age two years to the eighth decade). Ataxia, manifesting initially as poor balance when walking, is typically followed by upper-limb ataxia, dysarthria, dysphagia, peripheral motor and sensory neuropathy, spasticity, autonomic disturbance, and often abnormal eye movements and optic atrophy. Hypertrophic cardiomyopathy is present in about two thirds of individuals; occasionally it is diagnosed prior to the onset of ataxia. Diabetes mellitus and impaired glucose tolerance can also occur. Among individuals with FRDA, about 75% have "typical Friedreich ataxia" and about 25% of individuals with biallelic FXN full-penetrance GAA repeat expansions have "atypical Friedreich ataxia" that includes late-onset FRDA (LOFA) (i.e., onset after age 25 years), very late-onset FRDA (VLOFA) (i.e., onset after age 40 years), and FRDA with retained reflexes (FARR).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/383962">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_356134"><div><strong>Friedreich ataxia 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>356134</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.">C1865981</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Typical Friedreich ataxia (FRDA) is characterized by progressive ataxia with onset from early childhood to early adulthood with mean age at onset from 10 to 15 years (range: age two years to the eighth decade). Ataxia, manifesting initially as poor balance when walking, is typically followed by upper-limb ataxia, dysarthria, dysphagia, peripheral motor and sensory neuropathy, spasticity, autonomic disturbance, and often abnormal eye movements and optic atrophy. Hypertrophic cardiomyopathy is present in about two thirds of individuals; occasionally it is diagnosed prior to the onset of ataxia. Diabetes mellitus and impaired glucose tolerance can also occur. Among individuals with FRDA, about 75% have "typical Friedreich ataxia" and about 25% of individuals with biallelic FXN full-penetrance GAA repeat expansions have "atypical Friedreich ataxia" that includes late-onset FRDA (LOFA) (i.e., onset after age 25 years), very late-onset FRDA (VLOFA) (i.e., onset after age 40 years), and FRDA with retained reflexes (FARR).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/356134">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_357274"><div><strong>Pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>357274</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.">C1867407</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/357274">Condition Record</a></div></div>
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<div class="divPopper rprt" id="rdis_442697"><div><strong>Hereditary hypotrichosis with recurrent skin vesicles</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>442697</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.">C2751292</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
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<div class="spaceAbove">Hypotrichosis and recurrent skin vesicles (HYPTSV) is characterized by sparse to absent scalp hair, eyebrows, eyelashes, and body hair, as well as recurrent vesicles of scalp and skin. Some patients also exhibit trauma-induced blistering, and anomalies of dental enamel and of nails may be observed (Ayub et al., 2009; Onoufriadis et al., 2020).</div>
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<div class="spaceAbove nowrap">See: <a href="/medgen/442697">Condition Record</a></div></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_182959" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Becker muscular dystrophy</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_331805" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Bethlem myopathy</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_3925" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Duchenne muscular dystrophy</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_383962" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Friedreich ataxia 1</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_356134" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Friedreich ataxia 2</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (9)', 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_442697" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hereditary hypotrichosis with recurrent skin vesicles</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_254845" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Muscular dystrophy, cardiac type</a></div>
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<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_338087" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Nathalie syndrome</a></div>
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||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_357274" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities</a></div></span></div></div>
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</div>
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<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>
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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>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34039680">Diagnosis, management and therapeutic strategies for congenital long QT syndrome.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wilde AAM,
|
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Amin AS,
|
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Postema PG</span><br />
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<span class="medgenPMjournal">Heart</span>
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2022 Mar;108(5):332-338.
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Epub 2021 May 26
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doi: 10.1136/heartjnl-2020-318259.
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||
<span class="bold">PMID: </span><a href="/pubmed/34039680" target="_blank">34039680</a><a href="/pmc/articles/PMC8862104" 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/33382560">Eating Disorders in Primary Care: Diagnosis and Management.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Klein DA,
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Sylvester JE,
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Schvey NA</span><br />
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<span class="medgenPMjournal">Am Fam Physician</span>
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2021 Jan 1;103(1):22-32.
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<span class="bold">PMID: </span><a href="/pubmed/33382560" target="_blank">33382560</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28134952">Pectus Excavatum: A Review of Diagnosis and Current Treatment Options.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Abid I,
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Ewais MM,
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Marranca J,
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Jaroszewski DE</span><br />
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<span class="medgenPMjournal">J Am Osteopath Assoc</span>
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2017 Feb 1;117(2):106-113.
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doi: 10.7556/jaoa.2017.021.
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<span class="bold">PMID: </span><a href="/pubmed/28134952" target="_blank">28134952</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(abnormal%20ekg)%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 (1078)</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/37423027">Significance of electrocardiogram abnormalities in children presenting to the emergency department with acute COVID-19 infection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Van Hersh A,
|
||
Jawad K,
|
||
Feygin Y,
|
||
Johnsrude C,
|
||
Dasgupta S</span><br />
|
||
<span class="medgenPMjournal">Am J Emerg Med</span>
|
||
2023 Sep;71:195-199.
|
||
Epub 2023 Jun 28
|
||
doi: 10.1016/j.ajem.2023.06.041.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37423027" target="_blank">37423027</a><a href="/pmc/articles/PMC10299939" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33971558">Diagnostic value of electrocardiogram during routine electroencephalogram.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yassin A,
|
||
El-Salem K,
|
||
Khassawneh BY,
|
||
Al-Mistarehi AH,
|
||
Jarrah M,
|
||
Zein Alaabdin AM,
|
||
Abumurad SK,
|
||
Qasaimeh MG,
|
||
Bashayreh SY,
|
||
Kofahi RM,
|
||
Alhayk KA,
|
||
Alshorafat D,
|
||
Al Qawasmeh M</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2021 Jul;89:19-23.
|
||
Epub 2021 Apr 25
|
||
doi: 10.1016/j.seizure.2021.04.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33971558" target="_blank">33971558</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27308824">Chagas Cardiomyopathy: Usefulness of EKG and Echocardiogram in a Non-Endemic Country.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sánchez-Montalvá A,
|
||
Salvador F,
|
||
Rodríguez-Palomares J,
|
||
Sulleiro E,
|
||
Sao-Avilés A,
|
||
Roure S,
|
||
Valerio L,
|
||
Evangelista A,
|
||
Molina I</span><br />
|
||
<span class="medgenPMjournal">PLoS One</span>
|
||
2016;11(6):e0157597.
|
||
Epub 2016 Jun 16
|
||
doi: 10.1371/journal.pone.0157597.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27308824" target="_blank">27308824</a><a href="/pmc/articles/PMC4911085" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3944840">Electrocardiographic monitoring after electrical injury: necessity or luxury.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Purdue GF,
|
||
Hunt JL</span><br />
|
||
<span class="medgenPMjournal">J Trauma</span>
|
||
1986 Feb;26(2):166-7.
|
||
doi: 10.1097/00005373-198602000-00013.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3944840" target="_blank">3944840</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1080049">Antihypertensive drug therapy in USAF flying personnel.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">King WH,
|
||
Lancaster MC,
|
||
Cloyd DE</span><br />
|
||
<span class="medgenPMjournal">Aviat Space Environ Med</span>
|
||
1975 Apr;46(4 Sec 1):436-40.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1080049" target="_blank">1080049</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20EKG%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 (32)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37423027">Significance of electrocardiogram abnormalities in children presenting to the emergency department with acute COVID-19 infection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Van Hersh A,
|
||
Jawad K,
|
||
Feygin Y,
|
||
Johnsrude C,
|
||
Dasgupta S</span><br />
|
||
<span class="medgenPMjournal">Am J Emerg Med</span>
|
||
2023 Sep;71:195-199.
|
||
Epub 2023 Jun 28
|
||
doi: 10.1016/j.ajem.2023.06.041.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37423027" target="_blank">37423027</a><a href="/pmc/articles/PMC10299939" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33971558">Diagnostic value of electrocardiogram during routine electroencephalogram.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yassin A,
|
||
El-Salem K,
|
||
Khassawneh BY,
|
||
Al-Mistarehi AH,
|
||
Jarrah M,
|
||
Zein Alaabdin AM,
|
||
Abumurad SK,
|
||
Qasaimeh MG,
|
||
Bashayreh SY,
|
||
Kofahi RM,
|
||
Alhayk KA,
|
||
Alshorafat D,
|
||
Al Qawasmeh M</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2021 Jul;89:19-23.
|
||
Epub 2021 Apr 25
|
||
doi: 10.1016/j.seizure.2021.04.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33971558" target="_blank">33971558</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9932179">Basic electrocardiogram interpretation for the OR nurse.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hutchisson B,
|
||
Cossey S,
|
||
Wheeler R</span><br />
|
||
<span class="medgenPMjournal">AORN J</span>
|
||
1999 Jan;69(1):222-7, 229-39; quiz 240-2, 245-6.
|
||
doi: 10.1016/s0001-2092(06)62771-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9932179" target="_blank">9932179</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3944840">Electrocardiographic monitoring after electrical injury: necessity or luxury.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Purdue GF,
|
||
Hunt JL</span><br />
|
||
<span class="medgenPMjournal">J Trauma</span>
|
||
1986 Feb;26(2):166-7.
|
||
doi: 10.1097/00005373-198602000-00013.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3944840" target="_blank">3944840</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1080049">Antihypertensive drug therapy in USAF flying personnel.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">King WH,
|
||
Lancaster MC,
|
||
Cloyd DE</span><br />
|
||
<span class="medgenPMjournal">Aviat Space Environ Med</span>
|
||
1975 Apr;46(4 Sec 1):436-40.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1080049" target="_blank">1080049</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20EKG%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 (20)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/40022040">Reduction of subclinical acute cardiac injury through DIBH radiotherapy: a single-institution real-world clinical cohort analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang K,
|
||
Shen J,
|
||
Liang Y,
|
||
Meng X,
|
||
Yang B,
|
||
Ma J,
|
||
Hu K,
|
||
Qiu J,
|
||
Hou X,
|
||
Zhang F</span><br />
|
||
<span class="medgenPMjournal">BMC Cancer</span>
|
||
2025 Feb 28;25(1):373.
|
||
doi: 10.1186/s12885-025-13769-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/40022040" target="_blank">40022040</a><a href="/pmc/articles/PMC11869486" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38905896">Do breast implants not cause an increased rate of abnormal electrocardiograms (ECG)?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hashemzadeh M,
|
||
Aghdasi S,
|
||
Movahed MR</span><br />
|
||
<span class="medgenPMjournal">J Electrocardiol</span>
|
||
2024 Jul-Aug;85:69-71.
|
||
Epub 2024 Jun 19
|
||
doi: 10.1016/j.jelectrocard.2024.06.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38905896" target="_blank">38905896</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37302919">BNT162b2 immunization-related myocarditis in adolescents and consequent hospitalization: Report from a medical center.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yen CW,
|
||
Lee J,
|
||
Chang YT,
|
||
Lee EP,
|
||
Wu CT,
|
||
Chang YJ</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neonatol</span>
|
||
2023 Nov;64(6):659-666.
|
||
Epub 2023 May 24
|
||
doi: 10.1016/j.pedneo.2023.01.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37302919" target="_blank">37302919</a><a href="/pmc/articles/PMC10205643" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34752850">Predictors of Mortality within 24 Months of Initial Arteriovenous Access Creation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sowa P,
|
||
Blecha M</span><br />
|
||
<span class="medgenPMjournal">Ann Vasc Surg</span>
|
||
2022 Apr;81:258-266.
|
||
Epub 2021 Nov 6
|
||
doi: 10.1016/j.avsg.2021.08.045.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34752850" target="_blank">34752850</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23241423">Thromboembolic risks of recombinant factor VIIa Use in warfarin-associated intracranial hemorrhage: a case-control study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">H-Y CS,
|
||
Xuemei C,
|
||
G KR,
|
||
M BL,
|
||
V HG,
|
||
A SF,
|
||
K FS</span><br />
|
||
<span class="medgenPMjournal">BMC Neurol</span>
|
||
2012 Dec 15;12:158.
|
||
doi: 10.1186/1471-2377-12-158.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23241423" target="_blank">23241423</a><a href="/pmc/articles/PMC3538560" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20EKG%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 (13)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37423027">Significance of electrocardiogram abnormalities in children presenting to the emergency department with acute COVID-19 infection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Van Hersh A,
|
||
Jawad K,
|
||
Feygin Y,
|
||
Johnsrude C,
|
||
Dasgupta S</span><br />
|
||
<span class="medgenPMjournal">Am J Emerg Med</span>
|
||
2023 Sep;71:195-199.
|
||
Epub 2023 Jun 28
|
||
doi: 10.1016/j.ajem.2023.06.041.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37423027" target="_blank">37423027</a><a href="/pmc/articles/PMC10299939" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37302919">BNT162b2 immunization-related myocarditis in adolescents and consequent hospitalization: Report from a medical center.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yen CW,
|
||
Lee J,
|
||
Chang YT,
|
||
Lee EP,
|
||
Wu CT,
|
||
Chang YJ</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neonatol</span>
|
||
2023 Nov;64(6):659-666.
|
||
Epub 2023 May 24
|
||
doi: 10.1016/j.pedneo.2023.01.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37302919" target="_blank">37302919</a><a href="/pmc/articles/PMC10205643" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33971558">Diagnostic value of electrocardiogram during routine electroencephalogram.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yassin A,
|
||
El-Salem K,
|
||
Khassawneh BY,
|
||
Al-Mistarehi AH,
|
||
Jarrah M,
|
||
Zein Alaabdin AM,
|
||
Abumurad SK,
|
||
Qasaimeh MG,
|
||
Bashayreh SY,
|
||
Kofahi RM,
|
||
Alhayk KA,
|
||
Alshorafat D,
|
||
Al Qawasmeh M</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2021 Jul;89:19-23.
|
||
Epub 2021 Apr 25
|
||
doi: 10.1016/j.seizure.2021.04.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33971558" target="_blank">33971558</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31272753">Cardiomegaly on chest radiographs as a predictor of heart disease in the pediatric population.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dasgupta S,
|
||
Kelleman M,
|
||
Slesnick T,
|
||
Oster ME</span><br />
|
||
<span class="medgenPMjournal">Am J Emerg Med</span>
|
||
2020 May;38(5):855-859.
|
||
Epub 2019 Jun 25
|
||
doi: 10.1016/j.ajem.2019.06.045.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31272753" target="_blank">31272753</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9818672">Outcomes of children treated for Lyme disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang TJ,
|
||
Sangha O,
|
||
Phillips CB,
|
||
Wright EA,
|
||
Lew RA,
|
||
Fossel AH,
|
||
Fossel K,
|
||
Shadick NA,
|
||
Liang MH,
|
||
Sundel RP</span><br />
|
||
<span class="medgenPMjournal">J Rheumatol</span>
|
||
1998 Nov;25(11):2249-53.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9818672" target="_blank">9818672</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Abnormal%20EKG%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 (17)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37423027">Significance of electrocardiogram abnormalities in children presenting to the emergency department with acute COVID-19 infection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Van Hersh A,
|
||
Jawad K,
|
||
Feygin Y,
|
||
Johnsrude C,
|
||
Dasgupta S</span><br />
|
||
<span class="medgenPMjournal">Am J Emerg Med</span>
|
||
2023 Sep;71:195-199.
|
||
Epub 2023 Jun 28
|
||
doi: 10.1016/j.ajem.2023.06.041.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37423027" target="_blank">37423027</a><a href="/pmc/articles/PMC10299939" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37302919">BNT162b2 immunization-related myocarditis in adolescents and consequent hospitalization: Report from a medical center.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yen CW,
|
||
Lee J,
|
||
Chang YT,
|
||
Lee EP,
|
||
Wu CT,
|
||
Chang YJ</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neonatol</span>
|
||
2023 Nov;64(6):659-666.
|
||
Epub 2023 May 24
|
||
doi: 10.1016/j.pedneo.2023.01.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37302919" target="_blank">37302919</a><a href="/pmc/articles/PMC10205643" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
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<div class="nl"><a target="_blank" href="/pubmed/33971558">Diagnostic value of electrocardiogram during routine electroencephalogram.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yassin A,
|
||
El-Salem K,
|
||
Khassawneh BY,
|
||
Al-Mistarehi AH,
|
||
Jarrah M,
|
||
Zein Alaabdin AM,
|
||
Abumurad SK,
|
||
Qasaimeh MG,
|
||
Bashayreh SY,
|
||
Kofahi RM,
|
||
Alhayk KA,
|
||
Alshorafat D,
|
||
Al Qawasmeh M</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2021 Jul;89:19-23.
|
||
Epub 2021 Apr 25
|
||
doi: 10.1016/j.seizure.2021.04.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33971558" target="_blank">33971558</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31272753">Cardiomegaly on chest radiographs as a predictor of heart disease in the pediatric population.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dasgupta S,
|
||
Kelleman M,
|
||
Slesnick T,
|
||
Oster ME</span><br />
|
||
<span class="medgenPMjournal">Am J Emerg Med</span>
|
||
2020 May;38(5):855-859.
|
||
Epub 2019 Jun 25
|
||
doi: 10.1016/j.ajem.2019.06.045.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31272753" target="_blank">31272753</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27308824">Chagas Cardiomyopathy: Usefulness of EKG and Echocardiogram in a Non-Endemic Country.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Sánchez-Montalvá A,
|
||
Salvador F,
|
||
Rodríguez-Palomares J,
|
||
Sulleiro E,
|
||
Sao-Avilés A,
|
||
Roure S,
|
||
Valerio L,
|
||
Evangelista A,
|
||
Molina I</span><br />
|
||
<span class="medgenPMjournal">PLoS One</span>
|
||
2016;11(6):e0157597.
|
||
Epub 2016 Jun 16
|
||
doi: 10.1371/journal.pone.0157597.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27308824" target="_blank">27308824</a><a href="/pmc/articles/PMC4911085" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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