en کودکان کودکان گزارش مورد Case Report <span style="font-size:11pt"><span style="line-height:14.0pt"><span style="unicode-bidi:embed"><span calibri="" style="font-family:"><b><span new="" roman="" style="font-family:" times=""><span style="color:#660066">Background:</span></span></b><b> </b></span></span></span></span><br> <span style="font-size:11pt"><span style="text-justify:kashida"><span style="text-kashida:0%"><span style="line-height:200%"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="font-size:14.0pt"><span style="line-height:200%"><span style="font-family:&quot;Times New Roman&quot;,serif">Acid maltase deficiency is the cause of Pompe disease (PD), also known as glycogen storage disease type II, which can result in lysosomal glycogen storage. Children, adults, and newborns can all exhibit fundamental characteristics. We described a rare case of Pompe disease (PD) with leukodystrophy manifestations, who was referred two years prior by an orthopedist due to irregular walking.</span></span></span></span></span></span></span></span><br> &nbsp; Pompe disease, Glycogen storage disease, Hypertrophy. 51 54 http://crms.mubabol.ac.ir/browse.php?a_code=A-10-207-1&slc_lang=en&sid=1 Soroor Inaloo sinaloo@sums.ac.ir 10031947532846001989 10031947532846001989 No Pediatric Neurology Neonatal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran Atena Modanlou a.modanlu@gmail.com 10031947532846001990 10031947532846001990 Yes Pediatric Neurology Neonatal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran