Document Detail


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).
MedLine Citation:
PMID:  20452891     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Dieter Schmidt; H Agostini; M Schumacher
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  European journal of medical research     Volume:  15     ISSN:  0949-2321     ISO Abbreviation:  Eur. J. Med. Res.     Publication Date:  2010 Feb 
Date Detail:
Created Date:  2010-05-10     Completed Date:  2010-05-27     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9517857     Medline TA:  Eur J Med Res     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  89-91     Citation Subset:  IM    
Affiliation:
University Freiburg, Augenklinik, Killianstr. 5, 79106 Freiburg, Germany. Dieter.Schmidt@uniklinik-freiburg.de
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple / pathology*
Adult
Arteriovenous Malformations / pathology*
Follow-Up Studies
Humans
Intracranial Arteriovenous Malformations / pathology*
Magnetic Resonance Angiography
Male
Retinal Artery / abnormalities*
Retinal Vein / abnormalities*

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