Glycogen storage disease due to aldolase A deficiency

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Name:
Glycogen storage disease due to aldolase A deficiency
Description:
Glycogen storage disease due to aldolase A deficiency is an extremely rare glycogen storage disease (see this term) characterized by hemolytic anemia with or without myopathy or intellectual deficit. Myopathy can be severe enough to result in fatal rhabdomyolysis in some patients. A family with episodic rhabdomyolysis (triggered by fever) without hemolytic anemia has recently been reported.
ORPHAcode:
57
Synonyms:
GSD due to aldolase A deficiency
GSD type 12
GSD type XII
Glycogen storage disease type 12
Glycogen storage disease type XII
Glycogenosis due to aldolase A deficiency
Glycogenosis type 12
Glycogenosis type XII
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14