| Glycogen storage disease due to aldolase A deficiency (disorder) |
| Glycogen storage disease due to aldolase A deficiency |
| Glycogenosis due to aldolase A deficiency
Glycogen storage disease type 12
Glycogenosis type 12
Glycogenosis type XII
Glycogen storage disease type XII
|
| An extremely rare glycogen storage disease with characteristics of 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 been reported. |
| glycogeenstapelingsziekte door deficiëntie van aldolase A |
| glycogeenstapelingsziekte door aldolase A-deficiëntie
glycogenose type XII
glycogeenstapelingsziekte type 12
|
