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Case Studies | Radiological Sciences | Bulgaria | Volume 6 Issue 12, December 2017
Sturge-Weber Syndrome - Clinical Case Study
Sirakova K [6] | Minkin K. [3] | Matanov Sv. [2] | Ninov K. [2]
Abstract: Sturge-Weber syndrome (SWS) or encephelotrigeminal angiomatosis is a syndrome, characterized by local brain atrophy and calcifications in the cerebral cortex combined with ipsilateral Port Wine facial nevus in the area innervated by the nervus trigeminus. SWS is a rare syndrome having incidence of 1 in 20.000-50.000 people. It affects men and women equally. SWS is a sporadically occurring congenital malformation and the fetal cortical veins (during 4-8 gestational week) develop abnormality, i. e. they remain fetal. There is no evidence of hereditary transmission. As associated gene mutation was found in nucleotide transition in GNAQ on chromosome 9q21. The venous drainage from the superficial brain part is carried out through sinus sagitalis superior, and the deep veins through sinus cavernosus and straight sinus. Cortical veins serve as a liaison between the two vein systems that flow in an internal jugular vein.
Keywords: Sturge-Weber syndrome, epilepsy,
Edition: Volume 6 Issue 12, December 2017,
Pages: 1342 - 1345
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Case Studies, Radiological Sciences, India, Volume 12 Issue 4, April 2023
Pages: 787 - 792Clinico Radiological Correlation of Pediatric and Neonatal Seizures
Dr. Ankur Chandra [3] | Dr. Ashok Uppal | Dr Chapala Shashank
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Case Studies, Radiological Sciences, India, Volume 5 Issue 4, April 2016
Pages: 1304 - 1308Tuberous Sclerosis Complex Syndrome Cardiovascular and Renal Manifestation of Tuberous Sclerosis Complex and Summary of the Revised Diagnostic Criteria
Dr. Jainesh Dodia [3] | Dr. Brig K. Sahoo [4]