AI Article Synopsis
- 418 couples with recurrent miscarriages underwent karyotyping to investigate genetic factors.
- 4.78% of these couples had chromosome abnormalities like centric fusion, translocation, inversion, mosaicism, or fragility.
- 7.19% displayed normal chromosomal variants, such as inv(9) and 1qh+, which are generally considered benign.
Article Abstract
418 couples karyotyped because of recurrent miscarriages are reported. 4,78% showed chromosome aberrations (centric fusion, translocation, inversion, mosaicism or fragility of certain chromosome) and 7,19% had normal variants (inv(9), inv(1), 1qh+, 9qh+, etc.).
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