| Literature DB >> 9695090 |
A O Saatci1, G S Saylam, Z O Yasti, M Söylev, I Saatci, S Kavukçu, B Memişoğlu.
Abstract
Etiological investigation of a 15-year-old boy with left ophthalmic artery occlusion led us to a diagnosis of neurofibromatosis type I as there were numerous large cafe-au-lait spots, axillary freckling, and brain MRI changes consistent with a hamartoma. In light of the present case, ophthalmic artery occlusion may be a rare feature of neurofibromatosis type I besides more commonly described cerebrovascular changes.Entities:
Mesh:
Year: 1998 PMID: 9695090 DOI: 10.1076/opge.19.2.87.2322
Source DB: PubMed Journal: Ophthalmic Genet ISSN: 1381-6810 Impact factor: 1.803