Examples of 'glycogen storage disease' in a sentence
Meaning of "glycogen storage disease"
Glycogen storage disease refers to a group of inherited metabolic disorders characterized by the abnormal accumulation or breakdown of glycogen in the body. It is caused by deficiencies in enzymes that are involved in glycogen metabolism. These diseases can affect various organs and tissues, leading to a wide range of symptoms and complications
How to use "glycogen storage disease" in a sentence
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glycogen storage disease
Glycogen storage disease type viii.
Method of treating glycogen storage disease.
Glycogen storage disease type v.
Potential treatment strategy for glycogen storage disease.
Glycogen storage disease.
Placental involvement in glycogen storage disease type IV.
Glycogen storage disease type XI is a form of glycogen storage disease.
A deficiency muscle glycogen phosphorylase is known as glycogen storage disease type V McArdle Disease.
Patients with glycogen storage disease also present an increased risk for developing adenomas.
Glycogenolysis Glycogen synthase Glycogen storage disease.
Glycogen storage disease type III presents during infancy with hypoglycemia and failure to thrive.
Or maybe it 's a glycogen storage disease.
Glycogen storage disease type II.
Metabolic abnormalities, including uncontrolled diabetes or glycogen storage disease.
Treatment of glycogen storage disease type II.
See also
Adeno-associated virus vectors for treatment of glycogen storage disease.
An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity.
This is a hearty breed, though some may be prone to glycogen storage disease.
World 's first gene therapy for glycogen storage disease produces remarkable results.
Glycogen storage disease type 5 is a genetic disorder that prevents the body from breaking down glycogen.
A novel GBE1 gene variant in a child with glycogen storage disease type IV.
Pompe disease, Glycogen storage disease due to acid maltase deficiency.
The structure-function domain has not been studied in detail Chen and Burchell, Glycogen storage disease.
Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme GSY.
Jerrod Watts is a patient enrolled in the first clinical trial for Glycogen Storage Disease ( GSD ).
The glycogen storage disease type IV ( GSD IV ) is an inherited disorder of glucose metabolism.
Could be Wilson 's or maybe it 's a glycogen storage disease.
What about a glycogen storage disease like McArdle 's?
No fever . Could be Wilson 's or maybe it 's a glycogen storage disease.
Glycogen storage disease ( versus other storage disorders ).
The method of claim 5, wherein the glycogen storage disease is Pompe disease.
Glycogen storage disease is caused by a defect in glucose-6-phosphatase.
This means so much to the glycogen storage disease community, " says Weinstein.
Inherited diseases like Heamochromatosis, Wilson 's disease, Galactosemia, Glycogen storage disease.
What about a glycogen storage disease like McArdle 's? It explains the pain.
Amylo-1,6-glucosidase activity is deficient in glycogen storage disease type III.
Errors in this gene cause glycogen storage disease type II ( Pompe disease ).
Phosphoglucomutase-1 deficiency is known as glycogen storage disease type 14 GSD XIV.
Gabriel Hofstedter … born with glycogen storage disease type II, otherwise known as Pompe 's disease.
He characterized the condition now known as Glycogen storage disease type II in 1932.
With Guido Fanconi, he characterized Glycogen storage disease type XI in 1949.
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