Classical Hemophilia
Definition:Classical hemophilia is a medical condition where a person has trouble with blood clotting due to a lack of a specific protein called factor VIII. This condition is usually passed down from parents to children and occurs almost only in males.
Usage Instructions: When using the term "classical hemophilia," you can refer to it in a medical context, such as when discussing health conditions, genetics, or blood disorders.
Example Sentence: "John was diagnosed with classical hemophilia, which means he must be careful to avoid injuries that could cause excessive bleeding."
Advanced Usage: In more advanced discussions, you might talk about the treatment options available for classical hemophilia, such as factor replacement therapy, or discuss the genetic implications of the disorder.
Word Variants: 1. Hemophilia (general term for blood clotting disorders) 2. Factor VIII (the specific protein that is deficient in classical hemophilia)
Different Meanings:While "hemophilia" specifically refers to blood clotting disorders, the prefix "classical" indicates a specific type of hemophilia, distinguishing it from other forms, such as hemophilia B, which involves a deficiency in factor IX.
Synonyms: - Hemophilia A (another name for classical hemophilia) - Bleeding disorder
Idioms and Phrasal Verbs:There are no specific idioms or phrasal verbs directly related to "classical hemophilia." However, you might hear phrases like "to bleed out," which means to lose a lot of blood, often used in medical contexts.
Summary:Classical hemophilia is a blood disorder primarily affecting men due to a deficiency in factor VIII, leading to challenges with clotting.