WebButyrylcholinesterase deficiency is an enzyme disorder characterized by prolonged apnea after the application of muscle relaxants (suxamethonium or mivacurium) to patients in … WebDec 13, 2024 · Pseudocholinesterase deficiency, also known as butyrylcholinesterase deficiency, [] is an inherited enzyme abnormality that results in abnormally slow metabolic degradation of exogenous choline ester drugs such as succinylcholine and mivacurium. If there is a deficiency in the plasma activity of pseudocholinesterase, prolonged muscular …
Butyrylcholinesterase Deficiency via the BCHE Gene - Clinical test ...
WebJul 16, 2024 · Butyrylcholinesterase (BChE; EC 3.1.1.8) hydrolyzes acetylcholine (ACh) and shares 54% of its amino acid sequence with acetylcholinesterase (AChE; EC 3.1.1.7). 1 Serum BChE can detoxify xenobiotics (e.g., organophosphates, carbamate pesticides, cocaine), activate drugs such as bambuterol and heroin, 2–5 and hydrolyze a peptide … WebButyrylcholinesterase ELISA Kits. Provided below are ELISA kits targeting butyrylcholinesterase, a human protein encoded by BCHE. This protein is 602 amino acids long, with a mass of 68.4 kDa, and is a member of the Type-B carboxylesterase/lipase family. This is reported to be a secreted protein. pint to gr
Pseudocholinesterase deficiency - Diagnosis and …
WebJul 18, 2024 · Butyrylcholinesterase Deficiency via the BCHE Gene. GTR Test ID Help Each Test is a specific, orderable test from a particular laboratory, and is assigned a … WebButyrylcholinesterase (BChE) is an enzyme of the cholinergic system, a major branch of the autonomic system, and may provide a measure of autonomic (dys)function. This study was undertaken to evaluate BChE activity in infants and young children who had died from Sudden Infant Death or Sudden Unexpected Death. Methods: In this case-control study ... WebACHS. Acetylcholinesterase, RBC. 49230-6. Result Id. Test Result Name. Result LOINC Value. Applies only to results expressed in units of measure originally reported by the … pint to ml nursing