학술논문

Claude Syndrome in Childhood Associated with Probable Neuro-Behcet Disease.
Document Type
Academic Journal
Author
Yavuz P; Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey.; Solmaz I; Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey.; Kaya UA; Department of Pediatric Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.; Akgoz A; Department of Pediatric Radiology, Hacettepe University Faculty of Medicine, Ankara, Turkey.; Oguz KK; Department of Pediatric Radiology, Hacettepe University Faculty of Medicine, Ankara, Turkey.; Aytac S; Department of Pediatric Hematology, Hacettepe University Faculty of Medicine, Ankara Turkey.; Ozen S; Department of Pediatric Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.; Yalnizoglu D; Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Source
Publisher: Hippokrates Verlag Country of Publication: Germany NLM ID: 8101187 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1439-1899 (Electronic) Linking ISSN: 0174304X NLM ISO Abbreviation: Neuropediatrics Subsets: MEDLINE
Subject
Language
English
Abstract
Claude syndrome is a rare midbrain stroke syndrome characterized by ipsilateral third cranial nerve palsy and contralateral hemiataxia. So far, only a few cases have been reported in childhood. We present two children with Claude syndrome at 9 and 15 years of age. The typical clinical picture was consistent with brain magnetic resonance imaging findings. A thorough investigation regarding the underlying etiology revealed no definite diagnosis but clues suggestive of probable neuro-Behcet disease. Awareness of pediatric neurologists on arterial ischemic stroke has been increasing over the past decades, enabling timely diagnosis and appropriate management of rare childhood cases with midbrain stroke.
Competing Interests: None declared.
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