Literature DB >> 24771489

Undecussated superior cerebellar peduncles and absence of the dorsal transverse pontine fibers: a new axonal guidance disorder?

Charlotte F Kweldam1, Hilary Gwynn, Alpa Vashist, Alexander H Hoon, Thierry A G M Huisman, Andrea Poretti.   

Abstract

Axonal guidance disorders are a newly recognized group of diseases of the human central nervous system. These disorders are characterized by white matter tracts with abnormal course and failure to cross the midline or presence of ectopic white matter tracts. Diffusion tensor imaging (DTI) and fiber tractography are suitable neuroimaging tools to detect morphological abnormalities in the course, decussation, and location of white matter tracts. We report on a 6.5-year-old child with significant global developmental delay. Axial color-coded fractional anisotropy (FA)-maps revealed absence of (1) the midline "focal red dot" at the level of the pontomesencephalic junction representing absence of decussation of the superior cerebellar peduncles and (2) the dorsal component of the transverse pontine fibers. These findings are highly suggestive of an axonal guidance disorders. The complete neuroimaging phenotype of this child does not match well-known diseases with similar DTI findings. We show how DTI reveals important information of microstructural brain malformations that may go undetected or remains underestimated and consequently DTI may suggest the possible pathomechanism. We conclude that this child may be suffering from a not yet described subtype of an axonal guidance disorder.

Entities:  

Mesh:

Year:  2014        PMID: 24771489     DOI: 10.1007/s12311-014-0562-7

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  17 in total

1.  Color schemes to represent the orientation of anisotropic tissues from diffusion tensor data: application to white matter fiber tract mapping in the human brain.

Authors:  S Pajevic; C Pierpaoli
Journal:  Magn Reson Med       Date:  1999-09       Impact factor: 4.668

2.  Cerebral and cerebellar motor activation abnormalities in a subject with Joubert syndrome: functional magnetic resonance imaging (MRI) study.

Authors:  Melissa A Parisi; Joseph D Pinter; Ian A Glass; Katherine Field; Bernard L Maria; Phillip F Chance; Roderick K Mahurin; Steven C Cramer
Journal:  J Child Neurol       Date:  2004-03       Impact factor: 1.987

Review 3.  Molecular mechanisms of axon guidance.

Authors:  John K Chilton
Journal:  Dev Biol       Date:  2006-02-14       Impact factor: 3.582

4.  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

5.  Neurophysiologic characterization of motor and sensory projections in Joubert syndrome.

Authors:  Hugo Théoret; Joseph Gleeson; Alvaro Pascual-Leone
Journal:  Clin Neurophysiol       Date:  2013-07-29       Impact factor: 3.708

Review 6.  Midline axon guidance and human genetic disorders.

Authors:  L Izzi; F Charron
Journal:  Clin Genet       Date:  2011-07-25       Impact factor: 4.438

Review 7.  Human genetic disorders of axon guidance.

Authors:  Elizabeth C Engle
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-03       Impact factor: 10.005

8.  Analysis and classification of cerebellar malformations.

Authors:  Sandeep Patel; A James Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2002-08       Impact factor: 3.825

9.  Uncommon syndromes of cerebellar vermis aplasia. II: Tecto-cerebellar dysraphia with occipital encephalocele.

Authors:  R L Friede
Journal:  Dev Med Child Neurol       Date:  1978-12       Impact factor: 5.449

Review 10.  Human malformations of the midbrain and hindbrain: review and proposed classification scheme.

Authors:  Melissa A Parisi; William B Dobyns
Journal:  Mol Genet Metab       Date:  2003 Sep-Oct       Impact factor: 4.797

View more
  2 in total

1.  The spectrum of brainstem malformations associated to mutations of the tubulin genes family: MRI and DTI analysis.

Authors:  Filippo Arrigoni; Romina Romaniello; Denis Peruzzo; Andrea Poretti; Maria Teresa Bassi; Carlo Pierpaoli; Enza Maria Valente; Sara Nuovo; Eugen Boltshauser; Thierry André Gerard Marie Huisman; Fabio Triulzi; Renato Borgatti
Journal:  Eur Radiol       Date:  2018-07-31       Impact factor: 5.315

2.  Biallelic mutations in human DCC cause developmental split-brain syndrome.

Authors:  Saumya S Jamuar; Klaus Schmitz-Abe; Alissa M D'Gama; Marie Drottar; Wai-Man Chan; Maya Peeva; Sarah Servattalab; Anh-Thu N Lam; Mauricio R Delgado; Nancy J Clegg; Zayed Al Zayed; Mohammad Asif Dogar; Ibrahim A Alorainy; Abdullah Abu Jamea; Khaled Abu-Amero; May Griebel; Wendy Ward; Ed S Lein; Kyriacos Markianos; A James Barkovich; Caroline D Robson; P Ellen Grant; Thomas M Bosley; Elizabeth C Engle; Christopher A Walsh; Timothy W Yu
Journal:  Nat Genet       Date:  2017-02-27       Impact factor: 38.330

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.