Glycogen storage disease due to aldolase A deficiency
MONDO:0012747Glycogen storage disease due to aldolase A deficiency is an extremely rare glycogen storage disease 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.
Also known as: GSD due to aldolase A deficiency, GSD type 12, GSD type XII, glycogen storage disease due to aldolase A deficiency, glycogen storage disease type 12, glycogen storage disease type XII, glycogenosis due to aldolase A deficiency, glycogenosis type 12
11 clinical trials for this condition and its sub-types, 1 tagged with Glycogen storage disease due to aldolase A deficiency itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →-
Smartwatch signals may flag anemia, no needle needed
Diagnosis Not yet recruitingAnemia often goes unnoticed because diagnosis requires a blood draw. This study tests whether a wrist-worn smartwatch can identify people likely to have anemia by tracking blood flow, heart rate, oxygen, and movement. About 400 adults, with and without anemia, will wear the watch…
Sponsor: Peking Union Medical College Hospital • Aim: Diagnosis
Last updated Sep 03, 2026 00:00 UTC
-
Could a painless light sensor replace the needle for anemia screening?
Diagnosis Not yet recruitingThis study tests whether a non-invasive device that uses light to measure hemoglobin through the skin can accurately detect anemia. Researchers will compare its readings with standard blood tests in 150 adults in Jakarta. If the device proves reliable, it could offer a quick, pai…
Sponsor: Tarumanagara University • Aim: Diagnosis
Last updated Jul 17, 2026 00:00 UTC