Document Detail


Neurofibromatosis type I and unilateral ophthalmic artery occlusion.
MedLine Citation:
PMID:  9695090     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
A O Saatci; G S Saylam; Z O Yasti; M Söylev; I Saatci; S Kavukçu; B Memişoğlu
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Ophthalmic genetics     Volume:  19     ISSN:  1381-6810     ISO Abbreviation:  Ophthalmic Genet.     Publication Date:  1998 Jun 
Date Detail:
Created Date:  1998-10-01     Completed Date:  1998-10-01     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  9436057     Medline TA:  Ophthalmic Genet     Country:  NETHERLANDS    
Other Details:
Languages:  eng     Pagination:  87-91     Citation Subset:  IM    
Affiliation:
Department of Ophthalmology, Dokuz Eylül University, Izmir, Turkey.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Arterial Occlusive Diseases / diagnosis*,  etiology
Brain / pathology
Brain Diseases / diagnosis
Choroid / blood supply
Fluorescein Angiography
Fundus Oculi
Hamartoma / diagnosis
Humans
Magnetic Resonance Imaging
Male
Neurofibromatosis 1 / diagnosis*
Ophthalmic Artery / pathology*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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