The new cells can also provide the missing enzyme for someone with a storage disease.
The symptoms of glycogen storage disease, a hereditary illness that involves the inability to metabolize sugars properly, can vary widely and may mimic other disorders, Ms. Swain said.
Impaired glucose mobilization may be caused by adrenal insufficiency, severe liver disease, glycogen storage disease, severe infections, and starvation.
Chronic liver inflammation due to glycogen storage disease leads to the development of HCA and HCC.
But now, she had iron storage disease, a condition that also killed her mother.
Reports on pregnancies in women with glycogen storage disease type Ia (GSD-Ia) are scarce.
Mutations in the β-galactosidase gene cause the lysosomal storage disease GM1-gangliosidosis.
To investigate brain morphology and function in patients with glycogen storage disease type I (GSDI).
To investigate the hypothalamus-pituitary-thyroid axis in patients with glycogen storage disease type 1(GSD1).
Tumours occurring in the setting of glycogen storage disease may show diffuse increased attenuation of liver on CT images.
In humans, loss-of-function mutations of TRPML1 cause type IV mucolipidosis (ML-IV), a lysosomal storage disease (LSD).
