Williams Syndrome

Williams syndrome is a rare genetic condition, present from birth, that affects development and can involve different aspects of health, such as the heart, growth, and learning. It is usually accompanied by a characteristic profile in development and personality.

Common features: particular facial features, delays in some aspects of development, notable sociability, and, at times, cardiovascular abnormalities may be present.

How is it addressed? It requires comprehensive, multidisciplinary follow-up over time, tailored to each person's needs.

Which specialists take part? The pediatrician coordinates developmental follow-up, while the physical therapist and other therapists support specific areas depending on the case. If there is a diagnosis or suspicion in the family, being accompanied by a professional team helps provide the most appropriate support at each stage.