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COAGULATION DISORDERS

Coagulation defects (clotting factor deficiencies) may be inherited or acquired (Table 19.24), mainly including Hemophilia A and B-both being X-linked recessive, almost always seen in males only. Hemophilia C (fXI deficiency), parahemophilia (fV deficiency) and other coagulation defects are usually autosomal recessive and produce minor hemorrhagic disease.

19.12.1

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Source: Agrawal M.. Textbook of Pediatrics. 3rd ed. — CBS Publishers,2025. — 973 p.. 2025
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  1. Agrawal M.. Textbook of Pediatrics. 3rd ed. — CBS Publishers,2025. — 973 p., 2025