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<meta name="keywords" content="C0751173, disease or syndrome, glycogen storage disease type ii, infantile, infantile glycogen storage disease type ii, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="The non-classic form of infantile-onset Pompe disease usually appears by age 1. It is characterized by delayed motor skills (such as rolling over and sitting) and progressive muscle weakness. The heart may be abnormally large (cardiomegaly), but affected individuals usually do not experience heart failure. The muscle weakness in this disorder leads to serious breathing problems, and most children with non-classic infantile-onset Pompe disease live only into early childhood.\n\nThe late-onset type of Pompe disease may not become apparent until later in childhood, adolescence, or adulthood. Late-onset Pompe disease is usually milder than the infantile-onset forms of this disorder and is less likely to involve the heart. Most individuals with late-onset Pompe disease experience progressive muscle weakness, especially in the legs and the trunk, including the muscles that control breathing. As the disorder progresses, breathing problems can lead to respiratory failure.\n\nThe classic form of infantile-onset Pompe disease begins within a few months of birth. Infants with this disorder typically experience muscle weakness (myopathy), poor muscle tone (hypotonia), an enlarged liver (hepatomegaly), and heart defects. Affected infants may also fail to gain weight and grow at the expected rate (failure to thrive) and have breathing problems. If untreated, this form of Pompe disease leads to death from heart failure in the first year of life.\n\nResearchers have described three types of Pompe disease, which differ in severity and the age at which they appear. These types are known as classic infantile-onset, non-classic infantile-onset, and late-onset.\n\nPompe disease is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body's cells. The accumulation of glycogen in certain organs and tissues, especially muscles, impairs their ability to function normally." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Glycogen storage disease type II, infantile (Concept Id: C0751173)
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<!--
UID=148252
ConceptID=C0751173
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Glycogen storage disease type II, infantile</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>148252</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information."><span class="highlight" style="background-color:">C0751173</span></a></dd><dt><span class="dotprefix"></span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
<td>Glycogen Storage Disease Type II, Infantile; Infantile Glycogen Storage Disease Type II</td></tr>
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
<div class="portlet mgSection" id="ID_100">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln">The non-classic form of infantile-onset Pompe disease usually appears by age 1. It is characterized by delayed motor skills (such as rolling over and sitting) and progressive muscle weakness. The heart may be abnormally large (cardiomegaly), but affected individuals usually do not experience heart failure. The muscle weakness in this disorder leads to serious breathing problems, and most children with non-classic infantile-onset Pompe disease live only into early childhood.<br /><br />The late-onset type of Pompe disease may not become apparent until later in childhood, adolescence, or adulthood. Late-onset Pompe disease is usually milder than the infantile-onset forms of this disorder and is less likely to involve the heart. Most individuals with late-onset Pompe disease experience progressive muscle weakness, especially in the legs and the trunk, including the muscles that control breathing. As the disorder progresses, breathing problems can lead to respiratory failure.<br /><br />The classic form of infantile-onset Pompe disease begins within a few months of birth. Infants with this disorder typically experience muscle weakness (myopathy), poor muscle tone (hypotonia), an enlarged liver (hepatomegaly), and heart defects. Affected infants may also fail to gain weight and grow at the expected rate (failure to thrive) and have breathing problems. If untreated, this form of Pompe disease leads to death from heart failure in the first year of life.<br /><br />Researchers have described three types of Pompe disease, which differ in severity and the age at which they appear. These types are known as classic infantile-onset, non-classic infantile-onset, and late-onset.<br /><br />Pompe disease is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body's cells. The accumulation of glycogen in certain organs and tissues, especially muscles, impairs their ability to function normally. [from <a title="MedlinePlus Genetics" href="https://medlineplus.gov/genetics/" class="defSource" target="_blank">MedlinePlus Genetics</a>]</div>
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<div class="portlet mgSection" id="ID_118">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test,  </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test,  </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM,  </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>,  </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar  </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0017919[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=6639">C</a></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 Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=6639" ref="ncbi_uid=6639">V</a></span></span><span class="TLline"><a href="/medgen/6639" ref="tree=GTR&amp;ncbi_uid=6639&amp;link_uid=6639" title="View MedGen record for 'Glycogen storage disease'">Glycogen storage disease</a></span><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0268147[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=468559">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK55061/" ref="ncbi_uid=468559">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=468559" ref="ncbi_uid=468559">V</a></span></span><span class="TLline"><a href="/medgen/468559" ref="tree=GTR&amp;ncbi_uid=468559&amp;link_uid=468559" title="View MedGen record for 'Glycogen phosphorylase kinase deficiency'">Glycogen phosphorylase kinase deficiency</a></span><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C3694531[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=854172">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=854172" target="_blank" href="/omim/300798">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK55061/" ref="ncbi_uid=854172">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=854172" ref="ncbi_uid=854172">V</a></span></span><span class="TLline"><a href="/medgen/854172" ref="tree=GTR&amp;ncbi_uid=854172&amp;link_uid=854172" title="View MedGen record for 'Glycogen storage disease IXa1'">Glycogen storage disease IXa1</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0543514[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=107772">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=107772" target="_blank" href="/omim/172490">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK55061/" ref="ncbi_uid=107772">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=107772" ref="ncbi_uid=107772">V</a></span></span><span class="TLline"><a href="/medgen/107772" ref="tree=GTR&amp;ncbi_uid=107772&amp;link_uid=107772" title="View MedGen record for 'Glycogen storage disease IXb'">Glycogen storage disease IXb</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C2751643[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=442778">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=442778" target="_blank" href="/omim/172471">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK55061/" ref="ncbi_uid=442778">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=442778" ref="ncbi_uid=442778">V</a></span></span><span class="TLline"><a href="/medgen/442778" ref="tree=GTR&amp;ncbi_uid=442778&amp;link_uid=442778" title="View MedGen record for 'Glycogen storage disease IXc'">Glycogen storage disease IXc</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1845151[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=335112">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=335112" target="_blank" href="/omim/300559">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK55061/" ref="ncbi_uid=335112">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=335112" ref="ncbi_uid=335112">V</a></span></span><span class="TLline"><a href="/medgen/335112" ref="tree=GTR&amp;ncbi_uid=335112&amp;link_uid=335112" title="View MedGen record for 'Glycogen storage disease IXd'">Glycogen storage disease IXd</a></span></li></ul></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C2931743[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=419152">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=419152" target="_blank" href="/omim/150000">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=419152" ref="ncbi_uid=419152">V</a></span></span><span class="TLline"><a href="/medgen/419152" ref="tree=GTR&amp;ncbi_uid=419152&amp;link_uid=419152" title="View MedGen record for 'Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency'">Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C2752027[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=442873">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=442873" target="_blank" href="/omim/131370">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=442873" ref="ncbi_uid=442873">V</a></span></span><span class="TLline"><a href="/medgen/442873" ref="tree=GTR&amp;ncbi_uid=442873&amp;link_uid=442873" title="View MedGen record for 'Glycogen storage disease due to muscle beta-enolase deficiency'">Glycogen storage disease due to muscle beta-enolase deficiency</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0017922[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=6641">C</a></span><span class="chiclet Rcolor round" title="Research test"><a target="_blank" href="/gtr/tests/?term=C0017922[DISCUI]&amp;test_type=Research" ref="ncbi_uid=6641">R</a></span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=6641" target="_blank" href="/omim/232400">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK26372/" ref="ncbi_uid=6641">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=6641" ref="ncbi_uid=6641">V</a></span></span><span class="TLline"><a href="/medgen/6641" ref="tree=GTR&amp;ncbi_uid=6641&amp;link_uid=6641" title="View MedGen record for 'Glycogen storage disease type III'">Glycogen storage disease type III</a></span><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1968739[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=369842">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=369842" target="_blank" href="/omim/232400">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=369842" ref="ncbi_uid=369842">V</a></span></span><span class="TLline"><a href="/medgen/369842" ref="tree=GTR&amp;ncbi_uid=369842&amp;link_uid=369842" title="View MedGen record for 'Glycogen storage disease IIIa'">Glycogen storage disease IIIa</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1968740[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=369843">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=369843" target="_blank" href="/omim/232400">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=369843" ref="ncbi_uid=369843">V</a></span></span><span class="TLline"><a href="/medgen/369843" ref="tree=GTR&amp;ncbi_uid=369843&amp;link_uid=369843" title="View MedGen record for 'Glycogen storage disease IIIb'">Glycogen storage disease IIIb</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=369844" target="_blank" href="/omim/232400">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=369844" ref="ncbi_uid=369844">V</a></span></span><span class="TLline"><a href="/medgen/369844" ref="tree=GTR&amp;ncbi_uid=369844&amp;link_uid=369844" title="View MedGen record for 'Glycogen storage disease IIIc'">Glycogen storage disease IIIc</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=369845" target="_blank" href="/omim/232400">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline"><a href="/medgen/369845" ref="tree=GTR&amp;ncbi_uid=369845&amp;link_uid=369845" title="View MedGen record for 'Glycogen storage disease IIId'">Glycogen storage disease IIId</a></span></li></ul></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0268149[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=120613">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=120613" target="_blank" href="/omim/261670">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=120613" ref="ncbi_uid=120613">V</a></span></span><span class="TLline"><a href="/medgen/120613" ref="tree=GTR&amp;ncbi_uid=120613&amp;link_uid=120613" title="View MedGen record for 'Glycogen storage disease type X'">Glycogen storage disease type X</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C3150754[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=462104">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=462104" target="_blank" href="/omim/603942">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=462104" ref="ncbi_uid=462104">V</a></span></span><span class="TLline"><a href="/medgen/462104" ref="tree=GTR&amp;ncbi_uid=462104&amp;link_uid=462104" title="View MedGen record for 'Glycogen storage disease XV'">Glycogen storage disease XV</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0017920[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=6640">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1312/" ref="ncbi_uid=6640">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=6640" ref="ncbi_uid=6640">V</a></span></span><span class="TLline"><a href="/medgen/6640" ref="tree=GTR&amp;ncbi_uid=6640&amp;link_uid=6640" title="View MedGen record for 'Glycogen storage disease, type I'">Glycogen storage disease, type I</a></span><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0268146[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=78644">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=78644" target="_blank" href="/omim/232220">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1312/" ref="ncbi_uid=78644">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=78644" ref="ncbi_uid=78644">V</a></span></span><span class="TLline"><a href="/medgen/78644" ref="tree=GTR&amp;ncbi_uid=78644&amp;link_uid=78644" title="View MedGen record for 'Glucose-6-phosphate transport defect'">Glucose-6-phosphate transport defect</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C2919796[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=415885">C</a></span><span class="chiclet Rcolor round" title="Research test"><a target="_blank" href="/gtr/tests/?term=C2919796[DISCUI]&amp;test_type=Research&amp;redirect=true" ref="ncbi_uid=415885">R</a></span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=415885" target="_blank" href="/omim/232200">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1312/" ref="ncbi_uid=415885">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=415885" ref="ncbi_uid=415885">V</a></span></span><span class="TLline"><a href="/medgen/415885" ref="tree=GTR&amp;ncbi_uid=415885&amp;link_uid=415885" title="View MedGen record for 'Glycogen storage disease due to glucose-6-phosphatase deficiency type IA'">Glycogen storage disease due to glucose-6-phosphatase deficiency type IA</a></span></li></ul></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0017921[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=5340">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=5340" target="_blank" href="/omim/232300">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1261/" ref="ncbi_uid=5340">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=5340" ref="ncbi_uid=5340">V</a></span></span><span class="TLline"><a href="/medgen/5340" ref="tree=GTR&amp;ncbi_uid=5340&amp;link_uid=5340" title="View MedGen record for 'Glycogen storage disease, type II'">Glycogen storage disease, type II</a></span><ul><li class="matched_ds"><span class="TLline">Glycogen storage disease type II, infantile</span></li></ul></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0017923[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=6642">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=6642" target="_blank" href="/omim/232500">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK115333/" ref="ncbi_uid=6642">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=6642" ref="ncbi_uid=6642">V</a></span></span><span class="TLline"><a href="/medgen/6642" ref="tree=GTR&amp;ncbi_uid=6642&amp;link_uid=6642" title="View MedGen record for 'Glycogen storage disease, type IV'">Glycogen storage disease, type IV</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0017924[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=5341">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=5341" target="_blank" href="/omim/232600">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1344/" ref="ncbi_uid=5341">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=5341" ref="ncbi_uid=5341">V</a></span></span><span class="TLline"><a href="/medgen/5341" ref="tree=GTR&amp;ncbi_uid=5341&amp;link_uid=5341" title="View MedGen record for 'Glycogen storage disease, type V'">Glycogen storage disease, type V</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0017926[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=5342">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=5342" target="_blank" href="/omim/232800">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=5342" ref="ncbi_uid=5342">V</a></span></span><span class="TLline"><a href="/medgen/5342" ref="tree=GTR&amp;ncbi_uid=5342&amp;link_uid=5342" title="View MedGen record for 'Glycogen storage disease, type VII'">Glycogen storage disease, type VII</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0272066[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=82895">C</a></span><span class="chiclet Rcolor round" title="Research test"><a target="_blank" href="/gtr/tests/?term=C0272066[DISCUI]&amp;test_type=Research&amp;redirect=true" ref="ncbi_uid=82895">R</a></span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=82895" target="_blank" href="/omim/103850">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=82895" ref="ncbi_uid=82895">V</a></span></span><span class="TLline"><a href="/medgen/82895" ref="tree=GTR&amp;ncbi_uid=82895&amp;link_uid=82895" title="View MedGen record for 'HNSHA due to aldolase A deficiency'">HNSHA due to aldolase A deficiency</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C2752015[DISCUI]&amp;test_type=Clinical" ref="ncbi_uid=414536">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=414536" target="_blank" href="/omim/171900">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/NBK1332/" ref="ncbi_uid=414536">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&amp;from_uid=414536" ref="ncbi_uid=414536">V</a></span></span><span class="TLline"><a href="/medgen/414536" ref="tree=GTR&amp;ncbi_uid=414536&amp;link_uid=414536" title="View MedGen record for 'PGM1-congenital disorder of glycosylation'">PGM1-congenital disorder of glycosylation</a></span></li></ul></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/317955" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Disorder by Special Category">Non-Neoplastic Disorder by Special Category</a></span><ul><li><span class="TLline"><a href="/medgen/44376" ref="tree=MeSH" title="MedGen record for Metabolic disease">Metabolic disease</a></span><ul><li><span class="TLline"><a href="/medgen/472889" ref="tree=MeSH" title="MedGen record for Carbohydrate metabolism disease">Carbohydrate metabolism disease</a></span><ul><li><span class="TLline"><a href="/medgen/2825" ref="tree=MeSH" title="MedGen record for Inborn carbohydrate metabolic disorder">Inborn carbohydrate metabolic disorder</a></span><ul><li><span class="TLline"><a href="/medgen/6639" ref="tree=MeSH" title="MedGen record for Glycogen storage disease">Glycogen storage disease</a></span><ul><li><span class="TLline"><a href="/medgen/5340" ref="tree=MeSH" title="MedGen record for Glycogen storage disease, type II">Glycogen storage disease, type II</a></span><ul><li><span class="matched_ds">Glycogen storage disease type II, infantile</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
</div>
<div class="portlet mgSection" id="ID_105">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
<div class="nl"><a target="_blank" href="/pubmed/33554498">Advances in diagnosis and management of Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Davison JE</span><br />
<span class="medgenPMjournal">J Mother Child</span>
2020 Oct 2;24(2):3-8.
doi: 10.34763/jmotherandchild.20202402si.2001.000002.
<span class="bold">PMID: </span><a href="/pubmed/33554498" target="_blank">33554498</a><a href="/pmc/articles/PMC8518093" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/22173792">Consensus treatment recommendations for late-onset Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cupler EJ,
Berger KI,
Leshner RT,
Wolfe GI,
Han JJ,
Barohn RJ,
Kissel JT;
AANEM Consensus Committee on Late-onset Pompe Disease</span><br />
<span class="medgenPMjournal">Muscle Nerve</span>
2012 Mar;45(3):319-33.
Epub 2011 Dec 15
doi: 10.1002/mus.22329.
<span class="bold">PMID: </span><a href="/pubmed/22173792" target="_blank">22173792</a><a href="/pmc/articles/PMC3534745" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/16702877">Pompe disease diagnosis and management guideline.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kishnani PS,
Steiner RD,
Bali D,
Berger K,
Byrne BJ,
Case LE,
Crowley JF,
Downs S,
Howell RR,
Kravitz RM,
Mackey J,
Marsden D,
Martins AM,
Millington DS,
Nicolino M,
O'Grady G,
Patterson MC,
Rapoport DM,
Slonim A,
Spencer CT,
Tifft CJ,
Watson MS</span><br />
<span class="medgenPMjournal">Genet Med</span>
2006 May;8(5):267-88.
doi: 10.1097/01.gim.0000218152.87434.f3.
<span class="bold">PMID: </span><a href="/pubmed/16702877" target="_blank">16702877</a><a href="/pmc/articles/PMC3110959" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(glycogen%20storage%20disease%20type%20ii%2C%20infantile)%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 (195)</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/39227307">High-risk screening for late-onset Pompe disease in China: An expanded multicenter study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Jiao K,
Zhu B,
Chang X,
Guo J,
Fu J,
Song X,
Yu X,
Zhang X,
Dong J,
Yan W,
Luan X,
Wang Z,
Han H,
Du L,
Yu L,
Zhang Y,
Zhang J,
Chen Y,
Hu J,
Zhao Z,
Kang J,
Tan S,
Wang Z,
Mao S,
Qian F,
Luo R,
Liu C,
Huang Z,
Li G,
Li X,
Luo L,
Li D,
Zhou Y,
Hu X,
Yu X,
Shi Y,
Jiang J,
Zhang J,
Cheng N,
Wang N,
Xia X,
Yue D,
Gao M,
Xi J,
Luo S,
Lu J,
Zhao C,
Ke Q,
Ma M,
Zhu W</span><br />
<span class="medgenPMjournal">J Inherit Metab Dis</span>
2025 Jan;48(1):e12793.
Epub 2024 Sep 3
doi: 10.1002/jimd.12793.
<span class="bold">PMID: </span><a href="/pubmed/39227307" target="_blank">39227307</a></div>
<div class="nl"><a target="_blank" href="/pubmed/37679331">Glycogen storage diseases.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hannah WB,
Derks TGJ,
Drumm ML,
Grünert SC,
Kishnani PS,
Vissing J</span><br />
<span class="medgenPMjournal">Nat Rev Dis Primers</span>
2023 Sep 7;9(1):46.
doi: 10.1038/s41572-023-00456-z.
<span class="bold">PMID: </span><a href="/pubmed/37679331" target="_blank">37679331</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33554498">Advances in diagnosis and management of Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Davison JE</span><br />
<span class="medgenPMjournal">J Mother Child</span>
2020 Oct 2;24(2):3-8.
doi: 10.34763/jmotherandchild.20202402si.2001.000002.
<span class="bold">PMID: </span><a href="/pubmed/33554498" target="_blank">33554498</a><a href="/pmc/articles/PMC8518093" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30275469">Lysosomal storage diseases.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Platt FM,
d'Azzo A,
Davidson BL,
Neufeld EF,
Tifft CJ</span><br />
<span class="medgenPMjournal">Nat Rev Dis Primers</span>
2018 Oct 1;4(1):27.
doi: 10.1038/s41572-018-0025-4.
<span class="bold">PMID: </span><a href="/pubmed/30275469" target="_blank">30275469</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26290112">Myositis Mimics.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Michelle EH,
Mammen AL</span><br />
<span class="medgenPMjournal">Curr Rheumatol Rep</span>
2015 Oct;17(10):63.
doi: 10.1007/s11926-015-0541-0.
<span class="bold">PMID: </span><a href="/pubmed/26290112" target="_blank">26290112</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Glycogen%20storage%20disease%20type%20II%2C%20infantile%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 (535)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/37679331">Glycogen storage diseases.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hannah WB,
Derks TGJ,
Drumm ML,
Grünert SC,
Kishnani PS,
Vissing J</span><br />
<span class="medgenPMjournal">Nat Rev Dis Primers</span>
2023 Sep 7;9(1):46.
doi: 10.1038/s41572-023-00456-z.
<span class="bold">PMID: </span><a href="/pubmed/37679331" target="_blank">37679331</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32745073">Pompe disease: pathogenesis, molecular genetics and diagnosis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Taverna S,
Cammarata G,
Colomba P,
Sciarrino S,
Zizzo C,
Francofonte D,
Zora M,
Scalia S,
Brando C,
Curto AL,
Marsana EM,
Olivieri R,
Vitale S,
Duro G</span><br />
<span class="medgenPMjournal">Aging (Albany NY)</span>
2020 Aug 3;12(15):15856-15874.
doi: 10.18632/aging.103794.
<span class="bold">PMID: </span><a href="/pubmed/32745073" target="_blank">32745073</a><a href="/pmc/articles/PMC7467391" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31894075">The Glycogen Storage Disorders.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Marion RW,
Paljevic E</span><br />
<span class="medgenPMjournal">Pediatr Rev</span>
2020 Jan;41(1):41-44.
doi: 10.1542/pir.2018-0146.
<span class="bold">PMID: </span><a href="/pubmed/31894075" target="_blank">31894075</a></div>
<div class="nl"><a target="_blank" href="/pubmed/18929906">Pompe's disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">van der Ploeg AT,
Reuser AJ</span><br />
<span class="medgenPMjournal">Lancet</span>
2008 Oct 11;372(9646):1342-53.
doi: 10.1016/S0140-6736(08)61555-X.
<span class="bold">PMID: </span><a href="/pubmed/18929906" target="_blank">18929906</a></div>
<div class="nl"><a target="_blank" href="/pubmed/16702877">Pompe disease diagnosis and management guideline.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kishnani PS,
Steiner RD,
Bali D,
Berger K,
Byrne BJ,
Case LE,
Crowley JF,
Downs S,
Howell RR,
Kravitz RM,
Mackey J,
Marsden D,
Martins AM,
Millington DS,
Nicolino M,
O'Grady G,
Patterson MC,
Rapoport DM,
Slonim A,
Spencer CT,
Tifft CJ,
Watson MS</span><br />
<span class="medgenPMjournal">Genet Med</span>
2006 May;8(5):267-88.
doi: 10.1097/01.gim.0000218152.87434.f3.
<span class="bold">PMID: </span><a href="/pubmed/16702877" target="_blank">16702877</a><a href="/pmc/articles/PMC3110959" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Glycogen%20storage%20disease%20type%20II%2C%20infantile%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 (793)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/37759679">A Comprehensive Update on Late-Onset Pompe Disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Labella B,
Cotti Piccinelli S,
Risi B,
Caria F,
Damioli S,
Bertella E,
Poli L,
Padovani A,
Filosto M</span><br />
<span class="medgenPMjournal">Biomolecules</span>
2023 Aug 22;13(9)
doi: 10.3390/biom13091279.
<span class="bold">PMID: </span><a href="/pubmed/37759679" target="_blank">37759679</a><a href="/pmc/articles/PMC10526932" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/37184753">Cipaglucosidase Alfa: First Approval.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Blair HA</span><br />
<span class="medgenPMjournal">Drugs</span>
2023 Jun;83(8):739-745.
doi: 10.1007/s40265-023-01886-5.
<span class="bold">PMID: </span><a href="/pubmed/37184753" target="_blank">37184753</a><a href="/pmc/articles/PMC10184071" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33554498">Advances in diagnosis and management of Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Davison JE</span><br />
<span class="medgenPMjournal">J Mother Child</span>
2020 Oct 2;24(2):3-8.
doi: 10.34763/jmotherandchild.20202402si.2001.000002.
<span class="bold">PMID: </span><a href="/pubmed/33554498" target="_blank">33554498</a><a href="/pmc/articles/PMC8518093" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32962155">Pompe Disease: New Developments in an Old Lysosomal Storage Disorder.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Meena NK,
Raben N</span><br />
<span class="medgenPMjournal">Biomolecules</span>
2020 Sep 18;10(9)
doi: 10.3390/biom10091339.
<span class="bold">PMID: </span><a href="/pubmed/32962155" target="_blank">32962155</a><a href="/pmc/articles/PMC7564159" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/18929906">Pompe's disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">van der Ploeg AT,
Reuser AJ</span><br />
<span class="medgenPMjournal">Lancet</span>
2008 Oct 11;372(9646):1342-53.
doi: 10.1016/S0140-6736(08)61555-X.
<span class="bold">PMID: </span><a href="/pubmed/18929906" target="_blank">18929906</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Glycogen%20storage%20disease%20type%20II%2C%20infantile%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 (515)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/37679331">Glycogen storage diseases.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hannah WB,
Derks TGJ,
Drumm ML,
Grünert SC,
Kishnani PS,
Vissing J</span><br />
<span class="medgenPMjournal">Nat Rev Dis Primers</span>
2023 Sep 7;9(1):46.
doi: 10.1038/s41572-023-00456-z.
<span class="bold">PMID: </span><a href="/pubmed/37679331" target="_blank">37679331</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34836082">Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Derks TGJ,
Rodriguez-Buritica DF,
Ahmad A,
de Boer F,
Couce ML,
Grünert SC,
Labrune P,
López Maldonado N,
Fischinger Moura de Souza C,
Riba-Wolman R,
Rossi A,
Saavedra H,
Gupta RN,
Valayannopoulos V,
Mitchell J</span><br />
<span class="medgenPMjournal">Nutrients</span>
2021 Oct 27;13(11)
doi: 10.3390/nu13113828.
<span class="bold">PMID: </span><a href="/pubmed/34836082" target="_blank">34836082</a><a href="/pmc/articles/PMC8621617" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32962155">Pompe Disease: New Developments in an Old Lysosomal Storage Disorder.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Meena NK,
Raben N</span><br />
<span class="medgenPMjournal">Biomolecules</span>
2020 Sep 18;10(9)
doi: 10.3390/biom10091339.
<span class="bold">PMID: </span><a href="/pubmed/32962155" target="_blank">32962155</a><a href="/pmc/articles/PMC7564159" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30275469">Lysosomal storage diseases.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Platt FM,
d'Azzo A,
Davidson BL,
Neufeld EF,
Tifft CJ</span><br />
<span class="medgenPMjournal">Nat Rev Dis Primers</span>
2018 Oct 1;4(1):27.
doi: 10.1038/s41572-018-0025-4.
<span class="bold">PMID: </span><a href="/pubmed/30275469" target="_blank">30275469</a></div>
<div class="nl"><a target="_blank" href="/pubmed/18929906">Pompe's disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">van der Ploeg AT,
Reuser AJ</span><br />
<span class="medgenPMjournal">Lancet</span>
2008 Oct 11;372(9646):1342-53.
doi: 10.1016/S0140-6736(08)61555-X.
<span class="bold">PMID: </span><a href="/pubmed/18929906" target="_blank">18929906</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Glycogen%20storage%20disease%20type%20II%2C%20infantile%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 (395)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/39227307">High-risk screening for late-onset Pompe disease in China: An expanded multicenter study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Jiao K,
Zhu B,
Chang X,
Guo J,
Fu J,
Song X,
Yu X,
Zhang X,
Dong J,
Yan W,
Luan X,
Wang Z,
Han H,
Du L,
Yu L,
Zhang Y,
Zhang J,
Chen Y,
Hu J,
Zhao Z,
Kang J,
Tan S,
Wang Z,
Mao S,
Qian F,
Luo R,
Liu C,
Huang Z,
Li G,
Li X,
Luo L,
Li D,
Zhou Y,
Hu X,
Yu X,
Shi Y,
Jiang J,
Zhang J,
Cheng N,
Wang N,
Xia X,
Yue D,
Gao M,
Xi J,
Luo S,
Lu J,
Zhao C,
Ke Q,
Ma M,
Zhu W</span><br />
<span class="medgenPMjournal">J Inherit Metab Dis</span>
2025 Jan;48(1):e12793.
Epub 2024 Sep 3
doi: 10.1002/jimd.12793.
<span class="bold">PMID: </span><a href="/pubmed/39227307" target="_blank">39227307</a></div>
<div class="nl"><a target="_blank" href="/pubmed/38084761">Enzyme replacement therapy for late-onset Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Dalmia S,
Sharma R,
Ramaswami U,
Hughes D,
Jahnke N,
Cole D,
Smith S,
Remmington T</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2023 Dec 12;12(12):CD012993.
doi: 10.1002/14651858.CD012993.pub2.
<span class="bold">PMID: </span><a href="/pubmed/38084761" target="_blank">38084761</a><a href="/pmc/articles/PMC10714667" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31342611">GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Reuser AJJ,
van der Ploeg AT,
Chien YH,
Llerena J Jr,
Abbott MA,
Clemens PR,
Kimonis VE,
Leslie N,
Maruti SS,
Sanson BJ,
Araujo R,
Periquet M,
Toscano A,
Kishnani PS,
On Behalf Of The Pompe Registry Sites</span><br />
<span class="medgenPMjournal">Hum Mutat</span>
2019 Nov;40(11):2146-2164.
Epub 2019 Aug 7
doi: 10.1002/humu.23878.
<span class="bold">PMID: </span><a href="/pubmed/31342611" target="_blank">31342611</a><a href="/pmc/articles/PMC6852536" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/22173792">Consensus treatment recommendations for late-onset Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cupler EJ,
Berger KI,
Leshner RT,
Wolfe GI,
Han JJ,
Barohn RJ,
Kissel JT;
AANEM Consensus Committee on Late-onset Pompe Disease</span><br />
<span class="medgenPMjournal">Muscle Nerve</span>
2012 Mar;45(3):319-33.
Epub 2011 Dec 15
doi: 10.1002/mus.22329.
<span class="bold">PMID: </span><a href="/pubmed/22173792" target="_blank">22173792</a><a href="/pmc/articles/PMC3534745" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/15535432">alpha-glucosidase (CHO) (Genzyme).</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Lachmann RH</span><br />
<span class="medgenPMjournal">Curr Opin Investig Drugs</span>
2004 Oct;5(10):1101-10.
<span class="bold">PMID: </span><a href="/pubmed/15535432" target="_blank">15535432</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Glycogen%20storage%20disease%20type%20II%2C%20infantile%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 (467)</a></div></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln">
<div class="nl"><a target="_blank" href="/pubmed/39424261">Global birth prevalence of Pompe disease: A systematic review and meta-analysis.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Kong W,
Lu C,
Wang L</span><br />
<span class="medgenPMjournal">Neuroscience</span>
2024 Dec 17;563:167-174.
Epub 2024 Oct 16
doi: 10.1016/j.neuroscience.2024.09.043.
<span class="bold">PMID: </span><a href="/pubmed/39424261" target="_blank">39424261</a></div>
<div class="nl"><a target="_blank" href="/pubmed/38084761">Enzyme replacement therapy for late-onset Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Dalmia S,
Sharma R,
Ramaswami U,
Hughes D,
Jahnke N,
Cole D,
Smith S,
Remmington T</span><br />
<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
2023 Dec 12;12(12):CD012993.
doi: 10.1002/14651858.CD012993.pub2.
<span class="bold">PMID: </span><a href="/pubmed/38084761" target="_blank">38084761</a><a href="/pmc/articles/PMC10714667" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33386209">Cardiovascular disease in non-classic Pompe disease: A systematic review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">van Kooten HA,
Roelen CHA,
Brusse E,
van der Beek NAME,
Michels M,
van der Ploeg AT,
Wagenmakers MAEM,
van Doorn PA</span><br />
<span class="medgenPMjournal">Neuromuscul Disord</span>
2021 Feb;31(2):79-90.
Epub 2020 Nov 9
doi: 10.1016/j.nmd.2020.10.009.
<span class="bold">PMID: </span><a href="/pubmed/33386209" target="_blank">33386209</a></div>
<div class="nl"><a target="_blank" href="/pubmed/31405600">Systematic review of oral and craniofacial findings in patients with Fabry disease or Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Benz K,
Hahn P,
Hanisch M,
Lücke K,
Lücke T,
Jackowski J</span><br />
<span class="medgenPMjournal">Br J Oral Maxillofac Surg</span>
2019 Nov;57(9):831-838.
Epub 2019 Aug 9
doi: 10.1016/j.bjoms.2019.07.018.
<span class="bold">PMID: </span><a href="/pubmed/31405600" target="_blank">31405600</a></div>
<div class="nl"><a target="_blank" href="/pubmed/22173792">Consensus treatment recommendations for late-onset Pompe disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Cupler EJ,
Berger KI,
Leshner RT,
Wolfe GI,
Han JJ,
Barohn RJ,
Kissel JT;
AANEM Consensus Committee on Late-onset Pompe Disease</span><br />
<span class="medgenPMjournal">Muscle Nerve</span>
2012 Mar;45(3):319-33.
Epub 2011 Dec 15
doi: 10.1002/mus.22329.
<span class="bold">PMID: </span><a href="/pubmed/22173792" target="_blank">22173792</a><a href="/pmc/articles/PMC3534745" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Glycogen%20storage%20disease%20type%20II%2C%20infantile%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 (23)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0751173%5bDISCUI%5d&amp;filter=method%3A1%5F2" target="_blank">Enzyme assay (1)</a></li>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Glycogen%20storage%20disease%20type%20II,%20infantile" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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