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Neuropediatrics 2002; 33(4): 209-214
DOI: 10.1055/s-2002-34498
Original Article

Georg Thieme Verlag Stuttgart · New York

Rhombencephalosynapsis: Clinical Findings and Neuroimaging in 9 Children

S. P. Toelle1 , C. Yalcinkaya2 , N. Kocer2 , T. Deonna3 , W. C. G. Overweg-Plandsoen4 , T. Bast5 , R. Kalmanchey6 , P. Barsi7 , J. F. L. Schneider1 , A. Capone Mori1 , E. Boltshauser1
  • 1 University Children's Hospital, Zurich, Switzerland
  • 2 Department of Neurology, Cerrahpasa Medical School, Istanbul, Turkey
  • 3 University Children's Hospital, Lausanne, Switzerland
  • 4 Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands
  • 5 University Children's Hospital, Heidelberg, Germany
  • 6 University Children's Hospital, Budapest, Hungary
  • 7 National Institute of Psychiatry and Neurology, Budapest, Hungary
Weitere Informationen

Publikationsverlauf

Received: January 10, 2002

Accepted after Revision: May 18, 2002

Publikationsdatum:
07. Oktober 2002 (online)

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Abstract

Rhombencephalosynapsis is a rare congenital abnormality characterised by dorsal fusion of the cerebellar hemispheres, agenesis or hypogenesis of the vermis, fusion of dentate nuclei and superior cerebellar peduncles. We describe 9 children, aged 1.5 to 6 years, with rhombencephalosynapsis. Isolated rhombencephalosynapsis was found in 2 patients, hydrocephalus in 3 children and another 3 children had ventriculomegaly. Additional supratentorial abnormalities were documented in 5 patients. Clinical findings ranged from mild truncal ataxia and normal cognitive abilities to severe cerebral palsy and mental retardation. No correlation between clinical findings and magnetic resonance imaging could be established so far.

Key words

Rhombencephalosynapsis - Magnetic Resonance Imaging - Cerebellum - Ataxia - Hydrocephalus

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Prof. E. Boltshauser

Department of Neurology, University Children's Hospital

Steinwiesstrasse 75

8032 Zurich

Switzerland

eMail: eugen.boltshauser@kispi.unizh.ch