hemoglobin m disease
Hemoglobin M disease is a genetic disorder that affects the functioning of hemoglobin, the protein responsible for carrying oxygen in red blood cells. It is characterized by the presence of abnormal hemoglobin molecules that are more prone to oxidation, leading to a reduced ability to bind and transport oxygen. This can cause various symptoms, including cyanosis (a bluish discoloration of the skin), shortness of breath, and fatigue.
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