Literature DB >> 9695090

Neurofibromatosis type I and unilateral ophthalmic artery occlusion.

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.

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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


  1 in total

1.  Diagnosis and clinical course of ocular ischemic syndrome with retinal vascular abnormalities due to unilateral ocular artery and internal carotid artery stenosis in a child with neurofibromatosis type 1: a case report.

Authors:  Hiroaki Sakai; Kosuke Kawata; Jun Masuoka; Tomohisa Nishimura; Hiroshi Enaida
Journal:  BMC Ophthalmol       Date:  2020-10-23       Impact factor: 2.209

  1 in total

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