Chimaera 46, XX, 46, XY

Тодорхойлолт

A disease caused by XX and XY embryonic fusion or two distinct loss events of a sex chromosome from an XXY embryo early in development. This results in a subset of cells in the body having an XX karyotype, while other cells demonstrate an XY karyotype. This disease may present with abnormal genital development.

Дэд ангилал 2

• LD56.0Androgenetic chimaera›
• LD56.1Gynogenetic chimaera›