Bilateral facial and cervical port-wine stain and Sturge-Weber syndrome

References (10)

1. Sturge WA. A case of partial epilepsy apparently due to a lesion of one of the vasomotor centres of the brain. Trans Clin Soc Lond. 1879;12:162-7
2. Brouwer B, van der Hoeve J, Mahoney W. A fourth type of phakomatosis: Sturge Weber syndrome. Verh k Akad Wet Amst. 1937;36: 1
3. Mantelli F, Bruscolini A, La Cava M, Abdolrahimzadeh S, Lambiase A. Ocular manifestations of Sturge-Weber syndrome: pathogenesis, diagnosis, and management. Clin Ophthalmol. 2016;10:871-8
4. Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B et al. Sturge-Weber syndrome and port wine stains caused by somatic mutation in GNAQ. N Engl J Med. 2013;368:1971-9
5. Aita JA. Neurocutaneous Diseases. Springfield (IL): Charles C Thomas. 1966
6. Kanada KN, Merin MR, Munden A, Friedlander SF. A prospective study of cutaneous findings in newborns in the United States: correlation with race, ethnicity, and gestational status using updated classification and nomenclature. J Pediatr. 2012;161:240-5
7. Waelchli R, Aylett SE, Robinson K, Chong WK, Martinez AE, Kinsler VA. New vascular classification of port-wine stains: improving prediction. Br J Dermatol. 2014;171:861-7
8. Maraña Pérez AI, Ruiz-Falcó Rojas ML, Puertas Martín V, Domínguez Carral J, Carreras Sáez I, Duat Rodríguez A et al. Analysis of Sturge-Weber syndrome: a retrospective study of multiple associated variables. Neurologia. 2016;Mar 7. pii: S0213-4853(16)00024-4
9. Tallman B, Tan OT, Morelli JG. Location of port-wine stains and the likelihood of ophthalmic and/or central nervous system complications. Pediatrics. 1991;87:323-7
10. Bioxeda P, de Misa RF, Arrazola JM. [Facial angioma and the Sturge-Weber syndrome: a study of 121 cases]. Med Clin (Barc). 1993;101:1-4.