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Case Reports
Journal Article
Twenty-seven years follow-up of a patient with congenital retinocephalofacial vascular malformation syndrome and additional congenital malformations (Bonnet-Dechaume-Blanc syndrome or Wyburn-Mason syndrome).
European Journal of Medical Research 2010 Februrary 27
PURPOSE: Follow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome.
METHODS: MRI and cerebral angiography.
RESULTS: In a 36-year-old man, magnetic resonance imaging of the skull and cerebral angiography revealed left intracranial arteriovenous malformations. Follow-up observation of 27 years revealed no essential change of retinal and cerebral arteriovenous malformations. Additional congenital deficits in this patient were described.
CONCLUSION: Patients with retinal arteriovenous malformations should be early examined with neuroradiological methods.
METHODS: MRI and cerebral angiography.
RESULTS: In a 36-year-old man, magnetic resonance imaging of the skull and cerebral angiography revealed left intracranial arteriovenous malformations. Follow-up observation of 27 years revealed no essential change of retinal and cerebral arteriovenous malformations. Additional congenital deficits in this patient were described.
CONCLUSION: Patients with retinal arteriovenous malformations should be early examined with neuroradiological methods.
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