Sanfilippo Syndrome treatment in Magdalena Contreras

Sanfilippo syndrome, also called mucopolysaccharidosis type III, is a genetic disease in which the body does not properly break down certain molecules, which accumulate and mainly affect the nervous system.

Common manifestations: After an initially seemingly normal period, changes may be noticed in behavior, sleep and the development of skills during childhood.

Origin: It stems from an inherited disorder that reduces the function of an enzyme responsible for processing these substances within cells.

Which specialist treats it? The pediatrician observes the first signs and works together with genetics and pediatric neurology for support. If you notice sustained changes in your child's behavior or development, the most advisable thing is to have it evaluated by a professional.