Literature DB >> 17898198

Diffusion tensor imaging in Joubert syndrome.

A Poretti1, E Boltshauser, T Loenneker, E M Valente, F Brancati, K Il'yasov, T A G M Huisman.   

Abstract

BACKGROUND AND
PURPOSE: Neuropathologic findings and preliminary imaging studies demonstrated the absence of pyramidal tract and superior cerebellar peduncular decussation in individual patients with Joubert syndrome (JS). We hypothesized that functional-structural neuroimaging findings do not differ between the genetic forms of JS.
MATERIALS AND METHODS: MR imaging was performed with a 3T MR imaging-unit. Multiplanar T2- and T1-weighted imaging was followed by diffusion tensor imaging (DTI). Isotropic diffusion-weighted images, apparent diffusion coefficient maps, and color-coded fractional anisotropy maps, including tractography, were subsequently calculated.
RESULTS: In all 6 patients studied, DTI showed that the fibers of the superior cerebellar peduncles did not decussate in the mesencephalon and the corticospinal tract failed to cross in the caudal medulla. The patients represented various genetic forms of JS.
CONCLUSION: In JS, the fibers of the pyramidal tract and the superior cerebellar peduncles do not cross, irrespective of the underlying mutation.

Entities:  

Mesh:

Year:  2007        PMID: 17898198      PMCID: PMC8134246          DOI: 10.3174/ajnr.A0703

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  26 in total

1.  Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutations.

Authors:  N L Sicotte; G Salamon; D W Shattuck; N Hageman; U Rüb; N Salamon; A E Drain; J L Demer; E C Engle; J R Alger; R W Baloh; T Deller; J C Jen
Journal:  Neurology       Date:  2006-08-08       Impact factor: 9.910

2.  Microstructural and physiological features of tissues elucidated by quantitative-diffusion-tensor MRI.

Authors:  P J Basser; C Pierpaoli
Journal:  J Magn Reson B       Date:  1996-06

3.  Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome.

Authors:  Enza Maria Valente; Jennifer L Silhavy; Francesco Brancati; Giuseppe Barrano; Suguna Rani Krishnaswami; Marco Castori; Madeline A Lancaster; Eugen Boltshauser; Loredana Boccone; Lihadh Al-Gazali; Elisa Fazzi; Sabrina Signorini; Carrie M Louie; Emanuele Bellacchio; Enrico Bertini; Bruno Dallapiccola; Joseph G Gleeson
Journal:  Nat Genet       Date:  2006-05-07       Impact factor: 38.330

Review 4.  Cerebello-oculo-renal syndromes including Arima, Senior-Löken and COACH syndromes: more than just variants of Joubert syndrome.

Authors:  D Satran; M E Pierpont; W B Dobyns
Journal:  Am J Med Genet       Date:  1999-10-29

5.  The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome.

Authors:  Lekbir Baala; Stephane Romano; Rana Khaddour; Sophie Saunier; Ursula M Smith; Sophie Audollent; Catherine Ozilou; Laurence Faivre; Nicole Laurent; Bernard Foliguet; Arnold Munnich; Stanislas Lyonnet; Remi Salomon; Ferechte Encha-Razavi; Marie-Claire Gubler; Nathalie Boddaert; Pascale de Lonlay; Colin A Johnson; Michel Vekemans; Corinne Antignac; Tania Attie-Bitach
Journal:  Am J Hum Genet       Date:  2006-11-15       Impact factor: 11.025

6.  Uncommon syndromes of cerebellar vermis aplasia. I: Joubert syndrome.

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

7.  Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.

Authors:  Russell J Ferland; Wafaa Eyaid; Randall V Collura; Laura D Tully; R Sean Hill; Doha Al-Nouri; Ahmed Al-Rumayyan; Meral Topcu; Generoso Gascon; Adria Bodell; Yin Yao Shugart; Maryellen Ruvolo; Christopher A Walsh
Journal:  Nat Genet       Date:  2004-08-22       Impact factor: 38.330

8.  Linkage analysis in families with Joubert syndrome plus oculo-renal involvement identifies the CORS2 locus on chromosome 11p12-q13.3.

Authors:  Lesley C Keeler; Sarah E Marsh; Esther P Leeflang; Christopher G Woods; László Sztriha; Lihadh Al-Gazali; Aithala Gururaj; Joseph G Gleeson
Journal:  Am J Hum Genet       Date:  2003-08-13       Impact factor: 11.025

9.  The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome.

Authors:  Melissa A Parisi; Craig L Bennett; Melissa L Eckert; William B Dobyns; Joseph G Gleeson; Dennis W W Shaw; Ruth McDonald; Allison Eddy; Phillip F Chance; Ian A Glass
Journal:  Am J Hum Genet       Date:  2004-05-11       Impact factor: 11.025

Review 10.  Joubert syndrome: a review.

Authors:  J M Saraiva; M Baraitser
Journal:  Am J Med Genet       Date:  1992-07-01
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  40 in total

1.  Interpeduncular heterotopia in Joubert syndrome: a previously undescribed MR finding.

Authors:  I Harting; U Kotzaeridou; A Poretti; A Seitz; J Pietz; M Bendszus; E Boltshauser
Journal:  AJNR Am J Neuroradiol       Date:  2011-06-02       Impact factor: 3.825

Review 2.  Paediatric neuroimaging.

Authors:  Fabio Triulzi
Journal:  Neurol Sci       Date:  2008-10       Impact factor: 3.307

Review 3.  Clinical and molecular features of Joubert syndrome and related disorders.

Authors:  Melissa A Parisi
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

4.  Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients.

Authors:  A Poretti; T A G M Huisman; I Scheer; E Boltshauser
Journal:  AJNR Am J Neuroradiol       Date:  2011-06-16       Impact factor: 3.825

Review 5.  Uncrossed epileptic seizures in Joubert syndrome.

Authors:  Pedro López Ruiz; Maria Eugenia García García; Daniela Dicapua Sacoto; Alberto Marcos-Dolado
Journal:  BMJ Case Rep       Date:  2015-05-22

6.  Tectocerebellar dysraphia and occipital encephalocele associated with trisomy X: case report and review of the literature.

Authors:  Lissa C Goulart; Luiz A Ferreira-Filho; Mariana M da Silva; Israel S B Carneiro; Siderley S Carneiro; Osvaldo Vilela-Filho
Journal:  Childs Nerv Syst       Date:  2021-01-06       Impact factor: 1.475

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

Authors:  Charlotte F Kweldam; Hilary Gwynn; Alpa Vashist; Alexander H Hoon; Thierry A G M Huisman; Andrea Poretti
Journal:  Cerebellum       Date:  2014-08       Impact factor: 3.847

Review 8.  Primary cilia in the developing and mature brain.

Authors:  Alicia Guemez-Gamboa; Nicole G Coufal; Joseph G Gleeson
Journal:  Neuron       Date:  2014-05-07       Impact factor: 17.173

Review 9.  Joubert syndrome: insights into brain development, cilium biology, and complex disease.

Authors:  Dan Doherty
Journal:  Semin Pediatr Neurol       Date:  2009-09       Impact factor: 1.636

10.  Eye movement abnormalities in Joubert syndrome.

Authors:  Avery H Weiss; Dan Doherty; Melissa Parisi; Dennis Shaw; Ian Glass; James O Phillips
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-05-14       Impact factor: 4.799

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