Neurofibromatosis Type 1 treatment in Mexico City

Neurofibromatosis type 1 is a condition of genetic origin that predisposes a person to the formation of benign tumors along the nerves and to the appearance of characteristic signs on the skin. It is usually identified from childhood.

Common signs:

• Cafe-au-lait colored patches on the skin
• Small soft bumps on or under the skin
• Freckles in areas such as the armpits or groin

When is it advisable to seek care? The presence of several characteristic patches or bumps that grow in number deserves a careful checkup.

Which specialist treats it? The approach is usually joint: the geneticist studies the hereditary component, the dermatologist and the pediatric dermatologist assess the skin lesions, and the pediatrician oversees follow-up in children. Identifying these signs in time and consulting them with a professional makes for an orderly follow-up.