Literature DB >> 10642108

Rhombencephalosynapsis diagnosed in childhood: clinical and MRI findings.

O Danon1, M Elmaleh, B Boukobza, M Fohlen, K Hadjnacer, M Hassan.   

Abstract

Rhombencephalosynapsis is an unfrequent malformation of the posterior fossa essentially characterized by vermian agenesis or hypogenesis, fusion of the cerebellar hemispheres and fusion of the dentate nuclei. Supratentorial abnormalities are usually associated. No specific clinical syndrome can be described in relation with this disorder. We report a case diagnosed by MRI in a living patient.

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Year:  2000        PMID: 10642108     DOI: 10.1016/s0730-725x(99)00113-7

Source DB:  PubMed          Journal:  Magn Reson Imaging        ISSN: 0730-725X            Impact factor:   2.546


  3 in total

1.  Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis.

Authors:  F Démurger; L Pasquier; C Dubourg; V Dupé; I Gicquel; C Evain; L Ratié; S Jaillard; M Beri; B Leheup; J Lespinasse; D Martin-Coignard; S Mercier; C Quelin; P Loget; P Marcorelles; A Laquerrière; C Bendavid; S Odent; V David
Journal:  Mol Syndromol       Date:  2013-08-01

2.  Rhombencephalosynapsis: association with single umbilical artery.

Authors:  Veena Kalra; Suvasini Sharma; Ajay Garg
Journal:  Indian J Pediatr       Date:  2008-09-22       Impact factor: 1.967

3.  Atypical craniosynostosis with torticollis and neurological symptoms: a rhombencephalosynapsis sequence.

Authors:  Virve Koljonen; Junnu Leikola; Leena Valanne; Jyri Hukki
Journal:  Case Rep Med       Date:  2009-12-16
  3 in total

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