Sturge –Weber Syndrome – A Case Report

Title: Sturge –Weber Syndrome – A Case Report

Authors: Dr Selvakumar Subbaraman, Dr Senthilkumar Selvaraj

DOI: https://dx.doi.org/10.18535/jmscr/v5i7.41

Abstract

Sturge-Weber Syndrome or encephalotrigeminal angiomatosis is a rare congenital, non-familial disorder characterized by a congenital facial birthmark and neurological abnormalities. The GNAQ gene mutation is responsible for Sturge-Weber syndrome.

References

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2. Sudarsanam A., Ardern-Holmes S.L. Sturge–Weber syndrome: from the past to the present. Eur J Paediatr Neurol. 2014 May;18:257–266. [PubMed]

3. Enjolras O., Riche M.C., Merland J.J. Facial port-wine stains and Sturge–Weber syndrome. Pediatrics. 1985;76:48–51. [PubMed]

4. Marx R.E., Stern D. Quintessence Publishing Co, Inc.; Chicago, IL, USA: 2003. Oral and Maxillofacial Pathology: A Rationale for Diagnosis and Treatment; pp. 224–226.

5. Bioxeda P., de Misa R.F., Arrazola J.M. Facial angioma and the Sturge–Weber syndrome: a study of 121 cases. Med Clin (Barc) 1993;101:1–4. [PubMed]

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