Patau Syndrome treatment in León

Patau syndrome is a genetic condition that originates from the presence of an extra copy of chromosome 13, which affects the development of several organs and systems.

General features: It may be associated with abnormalities of the heart, the nervous system, and other structures, identifiable in the early stages of life or even during pregnancy.

How is it identified? It is usually suspected through prenatal studies and confirmed with genetic tests that analyze the chromosomes.

Which specialists treat it? The geneticist plays a central role in the diagnosis and family guidance, while the pediatrician and the cardiologist take part in the comprehensive follow-up of the child. When this condition is suspected, evaluation with a specialized team allows for better guidance for the family.