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Encephalotrigeminal Angiomatosis (Sturge-Weber Syndrome, Klippel-Trenaunay-Weber Syndrome)
This is part of a series of living documents published in the Asia-Pacific Journal of Ophthalmology with reviews ongoing for all time. An annual review of specific topics covered in the living documents or an annual update with expansion of these topics are planned. Readers of the Asia-Pacific Journal of Ophthalmology are cordially invited to join in by posting to this blog any comments or corrections in the review about Sturge-Weber Syndrome. If you have photos of all aspects of Sturge-Weber Syndrome to share, please email them to The discussion in my blog as well as the selected photos will be incorporated into the next issue or version of the article.
Monday, October 8, 2012
I would like to cordially invite you to join me in the discussion about Sturge-Weber Syndrome. Comments and corrections are most welcome. Any insightful ideas will be incorporated into the next version of the article.
About the Author

Robert Ritch
Dr. Robert Ritch holds the Shelley and Steven Einhorn Distinguished Chair in Ophthalmology and is Surgeon Director and Chief of Glaucoma Services at the New York Eye & Ear Infirmary, New York City and Professor of Ophthalmology at The New York Medical College, Valhalla, New York. He has devoted his career to broadening our understanding of the nature of glaucoma and innovation in the medical, laser, and surgical treatment of glaucoma.

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