Hyperglycinemia refers to a condition where glycine is elevated in the blood.
Types include:
- Propionic acidemia, also known as "ketotic glycinemia"
- Glycine encephalopathy, also known as "non-ketotic hyperglycinemia".
It may also be a misspelling of hyperglycemia.
Other articles related to "hyperglycinemia":
List Of Diseases (H) - Hy - Hyp - Hype - Hyperc–Hyperg
... cataracts Hypergeusia Hyperglycemia Hyperglycerolemia Hyperglycinemia, isolated nonketotic type 1 Hyperglycinemia, isolated nonketotic type 2 Hyperglycinemia, isolated nonketotic Hyperglycinemia ...
... cataracts Hypergeusia Hyperglycemia Hyperglycerolemia Hyperglycinemia, isolated nonketotic type 1 Hyperglycinemia, isolated nonketotic type 2 Hyperglycinemia, isolated nonketotic Hyperglycinemia ...
List Of Genetic Disorders - Full List
... to 21-hydroxylase deficiency Hyperchylomicronemia, familial Hyperglycinemia with ketoacidosis and leukopenia Hyperlipoproteinemia type I hyperoxaluria, primary hyperphenylalaninaemia ...
... to 21-hydroxylase deficiency Hyperchylomicronemia, familial Hyperglycinemia with ketoacidosis and leukopenia Hyperlipoproteinemia type I hyperoxaluria, primary hyperphenylalaninaemia ...
Glycine Encephalopathy
... Glycine encephalopathy (also known as non-ketotic hyperglycinemia or NKH) is a rare autosomal recessive disorder of glycine metabolism ... Glycine encephalopathy is sometimes referred to as "nonketotic hyperglycinemia" (NKH), as a reference to the biochemical findings seen in patients ...
... Glycine encephalopathy (also known as non-ketotic hyperglycinemia or NKH) is a rare autosomal recessive disorder of glycine metabolism ... Glycine encephalopathy is sometimes referred to as "nonketotic hyperglycinemia" (NKH), as a reference to the biochemical findings seen in patients ...
Glycine Encephalopathy (Nonketotic Hyperglycinemia)
... Glycine encephalopathy (also known as non-ketotic hyperglycinemia or NKH) is a rare autosomal recessive disorder of glycine metabolism ... is sometimes referred to as "nonketotic hyperglycinemia" (NKH), as a reference to the biochemical findings seen in patients with the disorder, and to ...
... Glycine encephalopathy (also known as non-ketotic hyperglycinemia or NKH) is a rare autosomal recessive disorder of glycine metabolism ... is sometimes referred to as "nonketotic hyperglycinemia" (NKH), as a reference to the biochemical findings seen in patients with the disorder, and to ...
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