What does glycine encephalopathy mean?
Definitions for glycine encephalopathy
glycine encephalopa·thy
This dictionary definitions page includes all the possible meanings, example usage and translations of the word glycine encephalopathy.
Wikipedia
Glycine encephalopathy
Glycine encephalopathy is a rare autosomal recessive disorder of glycine metabolism. After phenylketonuria, glycine encephalopathy is the second most common disorder of amino acid metabolism. The disease is caused by defects in the glycine cleavage system, an enzyme responsible for glycine catabolism. There are several forms of the disease, with varying severity of symptoms and time of onset. The symptoms are exclusively neurological in nature, and clinically this disorder is characterized by abnormally high levels of the amino acid glycine in bodily fluids and tissues, especially the cerebrospinal fluid. Glycine encephalopathy is sometimes referred to as "nonketotic hyperglycinemia" (NKH), as a reference to the biochemical findings seen in patients with the disorder, and to distinguish it from the disorders that cause "ketotic hyperglycinemia" (seen in propionic acidemia and several other inherited metabolic disorders). To avoid confusion, the term "glycine encephalopathy" is often used, as this term more accurately describes the clinical symptoms of the disorder.
Numerology
Chaldean Numerology
The numerical value of glycine encephalopathy in Chaldean Numerology is: 1
Pythagorean Numerology
The numerical value of glycine encephalopathy in Pythagorean Numerology is: 8
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"glycine encephalopathy." Definitions.net. STANDS4 LLC, 2024. Web. 29 Apr. 2024. <https://www.definitions.net/definition/glycine+encephalopathy>.
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