👉 Heterostrophy is a rare genetic disorder characterized by a mutation in the DNA sequence of the beta-2 microglobulin gene. This gene codes for a protein that plays a crucial role in blood clotting and platelet aggregation, but it has been shown to be mutated in several conditions including sickle cell anemia (HbA1C), sickle cell disease, and inherited hemophilia. The mutation results in the production of abnormal beta-2 microglobulin proteins, which can
