Glucose-6-Phosphate Dehydrogenase Deficiency treatment in Mérida

Glucose-6-phosphate dehydrogenase deficiency is a hereditary condition in which an enzyme that protects red blood cells is missing or reduced, which can lead to their destruction in the face of certain factors.

Possible triggers: Some infections, certain foods such as fava beans, or exposure to certain substances can promote the breakdown of red blood cells in people with this condition.

Signs to watch: Paleness, dark urine, tiredness, or yellowish coloring of the skin can indicate an episode that warrants evaluation.

Which specialist treats it? The hematologist, and in children the pediatric hematologist, is the reference for its study, while the geneticist helps understand the hereditary component. A professional evaluation allows you to learn which factors to avoid on an individual basis.