Literature DB >> 20449733

MRI with fibre tracking in Cogan congenital oculomotor apraxia.

Laura Merlini1, Maria I Vargas, Raoul De Haller, Bénédict Rilliet, Joel Fluss.   

Abstract

BACKGROUND: Congenital ocular motor apraxia (COMA) occasionally shares with Joubert syndrome (JS) and related disorders (JSRDs) a peculiar malformation, the 'molar tooth sign' (MTS). In JSRDs, the absence of superior cerebellar peduncles (SCP) decussation is reported.
OBJECTIVE: To investigate whether COMA demonstrates similar abnormal axonal pathways.
MATERIALS AND METHODS: Eight healthy age-matched controls, three children with clinical COMA and one child with clinical JSRD underwent examination with a 1.5-T MRI scanner. Diffusion-weighted imaging (DWI), colour-coded fractional anisotropy maps and three-dimensional diffusion tensor imaging (DTI) tractography of the cerebellorubral network were analyzed.
RESULTS: On DTI cartography, the 'red dot' originally supposed to represent the SCP decussation in the midbrain was present in controls as well in those with COMA but absent in the single case with JS. In none of the subjects including controls was 3-D FT able to depict the SCP decussation. When seeded, the red dot resulted in the ventral tegmental decussation (VTD). It was normal in controls and in patients with COMA but was absent in our single patient with JSRD. MTS was identified in alla patients with COMA and in the patient with JSRD.
CONCLUSION: MTS can be present in both COMA and JSRD but the underlying anatomy depicted by fibre tracking is distinct. The main difference is the integrity of the VTD in COMA.

Entities:  

Mesh:

Year:  2010        PMID: 20449733     DOI: 10.1007/s00247-010-1653-3

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  32 in total

1.  Fiber tract-based atlas of human white matter anatomy.

Authors:  Setsu Wakana; Hangyi Jiang; Lidia M Nagae-Poetscher; Peter C M van Zijl; Susumu Mori
Journal:  Radiology       Date:  2003-11-26       Impact factor: 11.105

2.  Probabilistic topography of human corpus callosum using cytoarchitectural parcellation and high angular resolution diffusion imaging tractography.

Authors:  Yi-Ping Chao; Kuan-Hung Cho; Chun-Hung Yeh; Kun-Hsien Chou; Jyh-Horng Chen; Ching-Po Lin
Journal:  Hum Brain Mapp       Date:  2009-10       Impact factor: 5.038

3.  Pontine tegmental cap dysplasia: MR imaging and diffusion tensor imaging features of impaired axonal navigation.

Authors:  P Jissendi-Tchofo; D Doherty; G McGillivray; R Hevner; D Shaw; G Ishak; R Leventer; A J Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2008-10-08       Impact factor: 3.825

4.  A simplified method to measure the diffusion tensor from seven MR images.

Authors:  P J Basser; C Pierpaoli
Journal:  Magn Reson Med       Date:  1998-06       Impact factor: 4.668

5.  "Joubert syndrome" revisited: key ocular motor signs with magnetic resonance imaging correlation.

Authors:  B L Maria; K B Hoang; R J Tusa; A A Mancuso; L M Hamed; R G Quisling; M T Hove; E B Fennell; M Booth-Jones; D M Ringdahl; A T Yachnis; G Creel; B Frerking
Journal:  J Child Neurol       Date:  1997-10       Impact factor: 1.987

6.  The rubrospinal and central tegmental tracts in man.

Authors:  P W Nathan; M C Smith
Journal:  Brain       Date:  1982-06       Impact factor: 13.501

7.  Congenital ocular motor apraxia: imaging findings.

Authors:  M A Sargent; K J Poskitt; J E Jan
Journal:  AJNR Am J Neuroradiol       Date:  1997 Nov-Dec       Impact factor: 3.825

8.  Congenital ocular motor apraxia: clinical and neuroradiological findings, and long-term intellectual prognosis.

Authors:  Akiko Kondo; Yoshiaki Saito; Florin Floricel; Yoshihiro Maegaki; Kousaku Ohno
Journal:  Brain Dev       Date:  2007-03-01       Impact factor: 1.961

9.  Familial congenital oculomotor apraxia: clinical and electro-oculographic features.

Authors:  Christophe Orssaud; Isabelle Ingster-Moati; Olivier Roche; Emmanuel Bui Quoc; Jean Louis Dufier
Journal:  Eur J Paediatr Neurol       Date:  2008-08-13       Impact factor: 3.140

10.  Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance.

Authors:  Peter G Barth; Charles B Majoie; Matthan W A Caan; Marian A J Weterman; Marten Kyllerman; Leo M E Smit; Richard A Kaplan; Richard H Haas; Frank Baas; Jan-Maarten Cobben; Bwee Tien Poll-The
Journal:  Brain       Date:  2007-08-09       Impact factor: 13.501

View more
  3 in total

Review 1.  Cerebellar Microstructural Abnormalities in Parkinson's Disease: a Systematic Review of Diffusion Tensor Imaging Studies.

Authors:  Maryam Haghshomar; Parnian Shobeiri; Seyed Arsalan Seyedi; Fatemeh Abbasi-Feijani; Amirhossein Poopak; Houman Sotoudeh; Arash Kamali; Mohammad Hadi Aarabi
Journal:  Cerebellum       Date:  2022-01-10       Impact factor: 3.648

Review 2.  Brainstem Diffusion Tensor Tractography and Clinical Applications in Pain.

Authors:  Yu Zhang; Ansgar J Furst
Journal:  Front Pain Res (Lausanne)       Date:  2022-03-24

3.  SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum.

Authors:  Valentina Serpieri; Fulvio D'Abrusco; Jennifer C Dempsey; Yong-Han Hank Cheng; Filippo Arrigoni; Janice Baker; Roberta Battini; Enrico Silvio Bertini; Renato Borgatti; Angela K Christman; Cynthia Curry; Stefano D'Arrigo; Joel Fluss; Michael Freilinger; Simone Gana; Gisele E Ishak; Vincenzo Leuzzi; Hailey Loucks; Filippo Manti; Nancy Mendelsohn; Laura Merlini; Caitlin V Miller; Ansar Muhammad; Sara Nuovo; Romina Romaniello; Wolfgang Schmidt; Sabrina Signorini; Sabrina Siliquini; Krzysztof Szczałuba; Gessica Vasco; Meredith Wilson; Ginevra Zanni; Eugen Boltshauser; Dan Doherty; Enza Maria Valente
Journal:  J Med Genet       Date:  2021-10-21       Impact factor: 5.941

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.