Sturge-Weber Syndrome treatment in León

Sturge-Weber syndrome is a rare disorder, present from birth, that mainly affects the skin, the eyes, and the nervous system, and is associated with a characteristic reddish mark on the face.

How it shows up: In addition to the skin mark, it may be accompanied by seizures, differences in neurological development, or eye involvement.

Where it comes from: It arises from a genetic change that occurs during development, and it is not usually inherited.

Who treats it? Ongoing care usually falls to the pediatrician and to pediatric neurology to monitor the nervous system, with support from genetics to pinpoint the origin. When a mark like this is identified along with other signs, it is advisable for a professional to carry out a detailed evaluation and guide the next steps.