Atypical Sturge-Weber syndrome requires confirmation.

[1]  P. Striano,et al.  Clinical features of Sturge-Weber syndrome without facial nevus: five novel cases. , 2013, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[2]  B. Giraudeau,et al.  Sturge‐Weber Syndrome in Patients with Facial Port‐Wine Stain , 2012, Pediatric dermatology.

[3]  L. Sztriha,et al.  Sturge-Weber syndrome without facial nevus: a case report and review of the literature. , 2000, Acta paediatrica.

[4]  E. Dirik,et al.  Sturge-Weber syndrome without facial nevus. , 2000, Pediatric neurology.

[5]  K. Plate Mechanisms of angiogenesis in the brain. , 1999, Journal of neuropathology and experimental neurology.

[6]  S. Pascual-Pascual,et al.  Sturge-Weber syndrome without facial nevus. , 1995, Neuropediatrics.

[7]  W. Weston,et al.  Location of port-wine stains and the likelihood of ophthalmic and/or central nervous system complications. , 1991, Pediatrics.

[8]  L. Maiuri,et al.  Sturge-Weber disease without facial nevus. , 1989, Journal of neurosurgical sciences.

[9]  S. Shankar,et al.  Sturge‐Weber‐Dimitri disease without facial nevus , 1987, Neurology.

[10]  R. Happle Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin. , 1987, Journal of the American Academy of Dermatology.

[11]  R. Michelucci,et al.  Sturge-Weber syndrome without port-wine facial nevus. Report of 2 cases studied by CT. , 1983, Child's brain.

[12]  E. Binet,et al.  Sturge-Weber Syndrome , 1978, Clinical pediatrics.