Determining common variants in patients with haemophilia A in South Vietnam and screening female carriers in their family members

Conclusions These findings were the first to provide important information about the presence of Inv22 and point mutation in Vietnamese patients with HA, the mothers and their female family members. It demonstrated that genetic diagnosis and counselling for HA carriers were essential factors for future improvements in comprehensive and equitable healthcare polices for patients with HA and FCs in Vietnam.

http://jcp.bmj.com/cgi/content/short/76/5/339?rss=1

Source: Journal of Clinical Pathology - April 19, 2023 Category: Pathology Authors: Nguyen, B. S. T., Le, X. T. T., Huynh, N., Nguyen, H. H., Truong Nguyen, C.-M., Nguyen, B. H. Tags: Open access Original research Source Type: research