دوره 7، شماره 1 - ( 4-1402 )
جلد 7 شماره 1 صفحات 54-51 |
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Inaloo S, Modanlou A. Early Onset Pompe and Leukoencephalopathy: A Case-Report Study. CRMS 2023; 7 (1) :51-54
URL: http://crms.mubabol.ac.ir/article-1-159-fa.html
URL: http://crms.mubabol.ac.ir/article-1-159-fa.html
Early Onset Pompe and Leukoencephalopathy: A Case-Report Study. Current Research in Medical Sciences. 1402; 7 (1) :51-54
چکیده: (2343 مشاهده)
Background:
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.
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.
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دریافت: 1402/4/9 | پذیرش: 1402/5/11 | انتشار: 1402/5/15
دریافت: 1402/4/9 | پذیرش: 1402/5/11 | انتشار: 1402/5/15
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