Pathophysiology, diagnosis, and management of glaucoma associated with Sturge–Weber syndrome

Author:

Javaid Usman,Ali Muhammad HassaanORCID,Jamal Samreen,Butt Nadeem Hafeez

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Reference50 articles.

1. Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE, Marchuk DA, Comi AM, Pevsner J (2013) Sturge–Weber syndrome and port-wine stains caused by somatic mutation in GNAQ. N Engl J Med 368(21):1971–1979

2. Sudarsanam A, Ardern-Holmes SL (2014) Sturge–Weber syndrome: from the past to the present. Eur J Paediatr Neurol 18(3):257–266

3. Sinha R (2016) Sturge-Weber syndrome-a literature review. Indian J Appl Res. 6(2):399–400

4. Tripathi AK, Khan MA, Deo K, Tripathi RM (2016) Oral and extraoral manifestations of Sturge–Weber syndrome: a rare finding. Saudi J Oral Sci 3(1):53

5. Parsa CF (2013) Focal venous hypertension as a pathophysiologic mechanism for tissue hypertrophy, port-wine stains, the Sturge–Weber syndrome, and related disorders: proof of concept with novel hypothesis for underlying etiological cause (an American Ophthalmological Society thesis). Trans Am Ophthalmol Soc 111:180

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