A rare case of primary congenital glaucoma in combination with neurofibromatosis 1: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology,General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s12886-015-0142-8.pdf
Reference12 articles.
1. O’Connor K. Primary congenital glaucoma: making strides in genetic testing, early detection and treatment. Insight. 2009;34:11.
2. Boyd KP, Korf BR, Theos A. Neurofibromatosis type 1. J Am Acad Dermatol. 2009;61:1–14.
3. Ferner RE, Huson SM, Thomas N, Moss C, Willshaw H, Evans DG. Guidelines for the diagnosis and management of individuals with neurofibromatosis 1. J Med Genet. 2007;44:81–8.
4. Stumpf D, Alksne J, Annegers J. Neurofibromatosis. Conference statement. National Institutes of Health Consensus Development Conference. Arch Neurol. 1988;45:575–8.
5. Wise JB, Patel SG, Shah JP. Management issues in massive pediatric facial plexiform neurofibroma with neurofibromatosis type 1. Head Neck. 2002;24:207–11.
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