In this section
Birthmarks and Vascular Anomalies Program
- Types of birthmarks
- Specialty programs and services
- Conditions
- Arteriovenous malformation (AVM)
- Capillary malformation (port wine stain)
- Congenital hemangioma
- Infantile hemangiomas
- Kasabach Merritt phenomenon
- Lymphatic malformation
- Multifocal lymphangioendotheliomatosis with thrombocytopenia (MLT)
- PHACE syndrome
- Sturge-Weber syndrome
- Venous malformation (VM)
- Clinical trials and research
- Locations
- Our specialists
- Patient stories
- Get a second opinion
- Contact birthmarks and vascular anomalies
Sturge-Weber syndrome
The first, most obvious sign of Sturge-Weber syndrome, is a baby born with a facial birthmark. It usually will cover at least one eyelid and the forehead. The mark will vary in color and size. In rare cases, there is no port wine stain. Neurological problems are caused by excessive blood vessel growth on the surface of the brain. Seizures are the most common early problem, often starting by 1 year of age. Developmental delay also may occur in varying degrees.
Other problems may affect:
- Eyes - Increased pressure within the eye (glaucoma) can also be present at birth or develop later. This affects about 30 percent of patients with Sturge-Weber, and also can happen without Sturge-Weber syndrome. It most often affects the eye with the port wine stain.
- Organs - other body organs can be affected, although this is rare
Contact us
Contact Birthmarks and Vascular Anomalies Program by email, postal mail, or phone:
(414) 266-3727
Get a second opinion
It's important to know what your options are. We can provide expert opinions to verify or give more information about an initial diagnosis. Contact us today.