Across
- 2. Medication used to stimulate clotting in some cases of hemophilia.
- 3. Permanent change in DNA sequence leading to genetic variation.
- 6. Common symptom in hemophilia due to inadequate clotting.
- 9. Proteins essential for blood clotting.
- 13. The process of blood clot formation.
- 14. Bleeding into joint spaces, common in hemophilia.
- 17. Individual affected by hemophilia.
- 20. Severe bleeding, a potential complication of hemophilia.
- 21. Medical care to manage or alleviate a condition.
- 23. Often experienced due to joint bleeding in hemophilia.
- 25. IX Protein deficient in Hemophilia B.
- 26. Identification of a disease through examination or tests.
- 27. Process of infusing missing clotting factors in hemophilia treatment.
Down
- 1. Genetic disorder that impairs the blood's ability to clot.
- 4. Antibodies neutralizing the effect of clotting factors in hemophilia.
- 5. Common symptom around joints in hemophilia.
- 7. Type of genetic trait requiring two copies to be expressed.
- 8. Preventive treatment to avoid bleeding episodes.
- 9. Protein forming blood clots.
- 10. Specialist studying genes, inheritance, and genetic variation.
- 11. Study of heredity and the variation of inherited characteristics.
- 12. X Protein involved in the coagulation cascade.
- 15. Liquid part of blood carrying blood cells and platelets.
- 16. Protein in red blood cells carrying oxygen.
- 18. Blood's semi-solid state, preventing excessive bleeding.
- 19. Passing down of genetic traits from parents to offspring.
- 20. Pockets of blood outside blood vessels due to internal bleeding.
- 22. Process of stopping bleeding.
- 24. Physical injury leading to bleeding in hemophilia.
- 25. VIII Protein deficient in Hemophilia A.