Comprehensive approach to hemophilia

نویسندگان

چکیده

Hemophilia A, B are X-linked recessive bleeding disorder that typically results from a deficiency of clotting factor VIII (FVIII) and IX (FIX). The severity the disease is determined according to FVIII FIX levels. A have similar symptoms both characterized by bleeding, particularly in large joints such as ankles, knees, elbows. Recurrent eventually causes progressive hemophilic arthropathy. Life-threatening hemorrhages may occur rarely. Treatment hemophilia has improved significantly recent years with concentrates. average life expectancy was

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ژورنال

عنوان ژورنال: Journal of health sciences and medicine

سال: 2022

ISSN: ['2636-8579']

DOI: https://doi.org/10.32322/jhsm.1108174