Examples of 'storage disease' in a sentence
Meaning of "storage disease"
storage disease: A group of genetic disorders characterized by the body's inability to break down certain substances, leading to their abnormal accumulation in cells or tissues
How to use "storage disease" in a sentence
Basic
Advanced
storage disease
Fibringogen storage disease is a extremely rare disorder.
Polish rats with a fatty acid storage disease.
Glycogen storage disease type viii.
Potential treatment strategy for glycogen storage disease.
Hemochromatosis is iron storage disease or iron overload.
Heredopathia atactica polyneuritiformis phytanic acid storage disease.
Having iron storage disease.
Traditionally atherosclerosis has been considered merely as a lipid storage disease.
Phytanic acid storage disease.
If the individual has symptoms clinically associated with a certain lysosomal storage disease.
Glycogen storage disease type v.
Infantile sialic acid storage disease.
It is a lysosomal storage disease which is commonly listed in the family of leukodystrophies.
Method of treating glycogen storage disease.
Lysosomal storage disease enzymes.
See also
Galactosialidosis is a lysosomal storage disease.
Glycogen storage disease.
Enzyme defects leading to bigger liver in children commonly named storage disease of liver.
Copper storage disease.
Viral gene therapy as treatment for cholesterol storage disease or disorder.
See storage disease.
Cholestrol ester storage disease.
Glycogen storage disease type XI is a form of glycogen storage disease.
It is a type of copper storage disease.
Patients with glycogen storage disease also present an increased risk for developing adenomas.
FD is considered a lysosomal storage disease.
The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme.
Deficiency in GCR activity results in a lysosomal storage disease referred to as Gaucher disease.
Glycogen storage disease type III presents during infancy with hypoglycemia and failure to thrive.
Placental involvement in glycogen storage disease type IV.
Glycogen storage disease type II.
A deficiency muscle glycogen phosphorylase is known as glycogen storage disease type V McArdle Disease.
Methods to treat the lysosomal storage disease can also include methods to treat Gaucher disease.
Glycogenolysis Glycogen synthase Glycogen storage disease.
Iron Storage Disease in captive tapirs.
Treatment of glycogen storage disease type II.
Metabolic abnormalities, including uncontrolled diabetes or glycogen storage disease.
However, there is no evidence of a storage disease associated with this complex.
In some embodiments, the disease is a lysosomal storage disease.
An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity.
It is the only x-linked lipid storage disease.
Glycogen storage disease type 5 is a genetic disorder that prevents the body from breaking down glycogen.
Polish rats with a fatty-acid storage disease.
The lysosomal storage disease is Gaucher 's disease.
Or maybe it 's a glycogen storage disease.
The lysosomal storage disease may be any of the diseases identified in Table 1 above.
Adeno-associated virus vectors for treatment of glycogen storage disease.
World 's first gene therapy for glycogen storage disease produces remarkable results.
The therapeutic approach is directed to Niemann-Pick disease, a lysosomal storage disease.
It 's called a lysosomal storage disease or LSD.
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Examples of using Storage
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