lysinemia

Friendly

Lysinemia is a medical term that refers to a condition in which the body cannot properly process an amino acid called lysine. Here’s a simple breakdown to help you understand it better:

Definition:

• Lysinemia (noun): A genetic condition where the body lacks certain enzymes needed to break down lysine, leading to an accumulation of this amino acid in the blood. This can result in symptoms like muscle weakness and developmental delays.

Usage Instructions:

• You can use "lysinemia" when discussing medical conditions, particularly those related to metabolic disorders. It is a specialized term, so it’s mostly used in medical contexts.

Example Sentence:

• "The doctor diagnosed the child with lysinemia after observing symptoms like weakness and developmental delays."

Advanced Usage:

• In more advanced discussions, you might encounter terms like metabolic disorder, enzyme deficiency, and amino acid metabolism when talking about lysinemia in a clinical setting.

Word Variants:

• Lysine (noun): The amino acid that is not being metabolized properly in lysinemia.
• Lysinemic (adjective): Pertaining to or affected by lysinemia.
  • Example: "The lysinemic patient requires a special diet."

Different Meaning:

• While "lysinemia" specifically refers to the medical condition, the word lysine itself simply refers to the amino acid, which is important for protein synthesis in the body.

Synonyms:

• There are no direct synonyms for "lysinemia" since it is a specific medical term. However, you might refer to it in a broader context as a metabolic disorder.

Related Idioms and Phrasal Verbs:

• There are no common idioms or phrasal verbs that directly relate to "lysinemia" because it is a technical medical term. However, you might hear the phrase "to break down" when discussing metabolism, as in "The body breaks down amino acids for energy."

Summary:

In summary, lysinemia is a specific condition related to the metabolism of lysine. It is important in medical discussions, particularly in relation to genetic disorders and metabolic functions.

Academic

Noun

1. an inborn error of metabolism in which the lack of certain enzymes leads to an inability to metabolize the amino acid lysine; characterized by muscular weakness and mental retardation