Pseudocholinesterase Deficiency Synonyms
Pseudocholinesterase deficiency is a genetic condition that affects the body's ability to break down certain medications and chemicals. It is also known by several other names, including:
- Butyrylcholinesterase Deficiency: This term refers to the deficiency of the enzyme butyrylcholinesterase, which is responsible for breaking down certain substances in the body.
- Plasma Cholinesterase Deficiency: Plasma cholinesterase is another name for pseudocholinesterase, so this synonym highlights the deficiency of this specific enzyme.
- Cholinesterase Atypical Variant: This term emphasizes the fact that individuals with pseudocholinesterase deficiency have an atypical variant of the cholinesterase enzyme.
- Hereditary Cholinesterase Deficiency: This synonym highlights the genetic nature of the condition, indicating that it is inherited from one or both parents.
- Cholinesterase Nonreactivity: This term describes the lack of reactivity or response of the cholinesterase enzyme in individuals with pseudocholinesterase deficiency.
- Cholinesterase Insensitivity: Similar to the previous synonym, this term emphasizes the reduced sensitivity of the cholinesterase enzyme in breaking down certain substances.
Pseudocholinesterase deficiency can lead to prolonged effects of certain medications, such as muscle relaxants and local anesthetics, which are normally broken down by the enzyme. It is important for individuals with this condition to inform their healthcare providers about their deficiency to avoid potential complications during medical procedures.