1. Ahn HS. Hong CU. Pediatrics, 8th ed. Seoul: Daehan Printing & Publishing Co;2004; 1040–4.
2. Menkes JH, Sernat HB. Child Neurology, 6th ed. Philadelphia: Lippincott Williams&Wilkins;2000; 859–84.
3. Behrman RE, Kliegman RM, Jenson HB. Nelson textbook of Pediatrics, 17th ed. Philadelphia: Saunders;2004; 2015–9.
4. Riccardi VM. Neurofibromatosis: Clinical heterogeneity. Curr Prob Cancer. 1982; 7:1–34.
Article
5. Ropper AH, Brown RH. Adams and Victor’s principles of neurology, 8th ed. New York: McGraw-Hill;2005; 868–71.
6. Saver S, Cestari DM. Neurofibromatosis type I: Genetics and clinical manifestations. Semin Ophthalmol. 2008; 23:45–51.
7. Kreusel KM. Ophthamological manifestation in VKL and NF I: pathological and diagnostic implications. Fam Cancer. 2005; 4:43–7.
8. National Institute of Health Consensus Development Conference. Neurofibromatosis: conference statement. Arch Neurol. 1988; 45:575–8.
9. Baser ME, Friedman JM, Wallace AJ, et al. Evaluation of clinical diagnostic criteria for neurofibromatosis 2. Neurology. 2002; 59:1759–65.
Article
10. Ruggieri M, Pavone P, Polizzi A, et al. Ophthalmological manifestations in segmental neurofibromatosis type1. Br J Ophthalmol. 2004; 88:1429–33.
11. Listernick R, Mancini AJ, Charrow J. Segmental neurofibro matosis in childhood. Am J Med Genet A. 2003; 121:132–5.
12. Gaonker CH, Mukherjee AK, Pokle M. Involvement of the eye and orbit in neurofibromatosis. Indian J Ophthalmol. 1992; 40:2–4.
13. Huson S, Jones D, Beck L. Ophthalmic manifestations of neurofibromatosis. Br J Ophthalmol. 1987; 71:235–8.
Article
14. Bosch MM, Boltshauser E, Harpes P, Landau K. Ophthalmo logic findings and long-term cource in patients with neurofibro matosis type 2. Am J Ophthalmol. 2006; 141:1068–77.
15. Kim YH, Cho BC, Ko HK. 2 Cases of Neurofibromatosis. J Korean Ophthalmol Soc. 1982; 23:859–65.
16. Kwon IT, Ohn YH, Shin HH. Retinal Finding of a Case of Neurofibromatosis. J Korean Ophthalmol Soc. 1994; 35:210–4.
17. Yoon SW, Ahn BC. A Case of Orbital Neurilemoma Associated with Neurofibroma tosis. J Korean Ophthalmol Soc. 1999; 40:1993–7.
18. Jung JW, Lee JH, Shyn KH, Chi MJ. A Case of Plexiform Neurofibroma with Severe Ptosis and Proptosis. J Korean Ophthalmol Soc. 2007; 48:725–30.
19. Lee KH, Park JW, Yoon KC. A Case of Neurofibromatosis of the Orbit and Ocular Surface. J Korean Ophthalmol Soc. 2007; 48:1276–80.
Article
20. Ferner RE. Neurofibromatosis 1 and neurofibromatosis 2: a twenty first century perspective. Lancet Neurol. 2007; 6:340–51.
Article
21. Richetta A, Giustini S, Recupero SM, et al. Lisch nodules of the iris in neurofibromatosis type 1. J Eur Acad Dermatol Venereol. 2004; 18:342–4.
Article
22. Albert DM, Green WR, Zimbric ML, et al. Iris melanocyte numbers in Asian, African-American, and Caucacian irides. Trans Am Ophthalmol Soc. 2003; 101:217–22.
23. Arigon V, Binaghi M, Sabouret C, et al. Usefulness of systematic ophthalmologic investigations in neurofibromatosis 1: a cross sectional study of 211 patients. Eur J Ophthalmol. 2002; 12:413–8.
24. Huson S, Jones D, Beck L. Ophthalmic manifestations of neurofibromatosis. Br J Ophthalmol. 1987; 71:235–8.
Article
25. Payne MS, Nadell JM, Lacassie Y, Tilton AH. Congenital glaucoma and neurofibromatosis in a monozygotic twin: case report and review of the literature. J Child Neurolol. 2003; 18:504–8.
Article
26. Rosser T, Packer RJ. Intracranial neoplasms in children with neurofibromatosis 1. J Child Neurol. 2002; 17:630–7.
27. Ruggieri M, Huson SM. The clinical and diagnostic implications of mosaicism in the neurofibromatoses. Neurology. 2001; 56:1434–43.
28. Uhrin SR. Segmental neurofibromatosis. South Med J. 1980; 73:526–7.
29. Tinschert S, Naumann I, Stegmann E, et al. Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene. Eur J Hum Genet. 2000; 8:455–9.
30. Radtke HB, Sebold CD, Allison C, et al. Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors. J Genet Couns. 2007; 16:387–407.
Article
31. Messiaen LM, Callens T, Mortier G, et al. Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. Hum Mutat. 2000; 15:541–55.