Literature DB >> 21680654

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

A Poretti1, T A G M Huisman, I Scheer, E Boltshauser.   

Abstract

VH and MTS are the neuroimaging hallmarks of JSRD. We aimed to look at the full spectrum of neuroimaging findings in JSRD and reviewed the MR imaging of 75 patients with JSRD, including 13 siblings and 4 patients with OFD VI. All patients had VH and enlargement of the fourth ventricle. The degree of VH and the form of the MTS were variable. In most patients, the cerebellar hemispheres were normal and the PF was enlarged. Brain stem morphology was abnormal in 30% of the patients. Supratentorial findings included hippocampal malrotation, callosal dysgenesis, migration disorders, cephaloceles, and ventriculomegaly. All patients with OFD VI had a similar pattern, including HH in 2 patients. No neuroimaging-genotype correlation could be found. The wide neuroimaging spectrum in our patients supports the heterogeneity of JSRD. Neuroimaging differences in siblings represent intrafamilial heterogeneity. Due to the absence of a correlation with genotype, neuroimaging findings are of limited value in classifying patients with JSRD.

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Year:  2011        PMID: 21680654      PMCID: PMC7964342          DOI: 10.3174/ajnr.A2517

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


  17 in total

Review 1.  Joubert Syndrome and related disorders.

Authors:  Francesco Brancati; Bruno Dallapiccola; Enza Maria Valente
Journal:  Orphanet J Rare Dis       Date:  2010-07-08       Impact factor: 4.123

2.  Brain stem and cerebellar findings in Joubert syndrome.

Authors:  Ibrahim A Alorainy; Sohail Sabir; Mohammed Z Seidahmed; Hamid A Farooqu; Mustafa A Salih
Journal:  J Comput Assist Tomogr       Date:  2006 Jan-Feb       Impact factor: 1.826

3.  Diffusion tensor imaging in Joubert syndrome.

Authors:  A Poretti; E Boltshauser; T Loenneker; E M Valente; F Brancati; K Il'yasov; T A G M Huisman
Journal:  AJNR Am J Neuroradiol       Date:  2007-09-26       Impact factor: 3.825

Review 4.  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

5.  Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation.

Authors:  M Joubert; J J Eisenring; J P Robb; F Andermann
Journal:  Neurology       Date:  1969-09       Impact factor: 9.910

6.  Joubert syndrome with associated corpus callosum agenesis.

Authors:  N Zamponi; B Rossi; A Messori; G Polonara; L Regnicolo; C Cardinali
Journal:  Eur J Paediatr Neurol       Date:  2002       Impact factor: 3.140

7.  Magnetic resonance imaging features and classification of central nervous system malformations in Joubert syndrome.

Authors:  R G Quisling; A J Barkovich; B L Maria
Journal:  J Child Neurol       Date:  1999-10       Impact factor: 1.987

Review 8.  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

9.  Meckel syndrome in the Hutterite population is actually a Joubert-related cerebello-oculo-renal syndrome.

Authors:  Kym M Boycott; Jillian S Parboosingh; James N Scott; D Ross McLeod; Cheryl R Greenberg; T Mary Fujiwara; Jean K Mah; Julian Midgley; Andrew Wade; Francois P Bernier; Bernard N Chodirker; Martin Bunge; A Micheil Innes
Journal:  Am J Med Genet A       Date:  2007-08-01       Impact factor: 2.802

10.  Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes.

Authors:  Joseph G Gleeson; Lesley C Keeler; Melissa A Parisi; Sarah E Marsh; Phillip F Chance; Ian A Glass; John M Graham; Bernard L Maria; A James Barkovich; William B Dobyns
Journal:  Am J Med Genet A       Date:  2004-03-01       Impact factor: 2.802

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  58 in total

Review 1.  Inherited cerebellar ataxia in childhood: a pattern-recognition approach using brain MRI.

Authors:  L Vedolin; G Gonzalez; C F Souza; C Lourenço; A J Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2012-05-17       Impact factor: 3.825

2.  Can Latent Class Analysis Be Used to Improve the Diagnostic Process in Pediatric Patients with Chronic Ataxia?

Authors:  Samantha Klassen; Brenden Dufault; Michael S Salman
Journal:  Cerebellum       Date:  2017-04       Impact factor: 3.847

Review 3.  The genetics of cerebellar malformations.

Authors:  Kimberly A Aldinger; Dan Doherty
Journal:  Semin Fetal Neonatal Med       Date:  2016-05-07       Impact factor: 3.926

4.  Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.

Authors:  R Bachmann-Gagescu; J C Dempsey; I G Phelps; B J O'Roak; D M Knutzen; T C Rue; G E Ishak; C R Isabella; N Gorden; J Adkins; E A Boyle; N de Lacy; D O'Day; A Alswaid; Radha Ramadevi A; L Lingappa; C Lourenço; L Martorell; À Garcia-Cazorla; H Ozyürek; G Haliloğlu; B Tuysuz; M Topçu; P Chance; M A Parisi; I A Glass; J Shendure; D Doherty
Journal:  J Med Genet       Date:  2015-06-19       Impact factor: 6.318

5.  Consensus paper: radiological biomarkers of cerebellar diseases.

Authors:  Leonardo Baldarçara; Stuart Currie; M Hadjivassiliou; Nigel Hoggard; Allison Jack; Andrea P Jackowski; Mario Mascalchi; Cecilia Parazzini; Kathrin Reetz; Andrea Righini; Jörg B Schulz; Alessandra Vella; Sara Jane Webb; Christophe Habas
Journal:  Cerebellum       Date:  2015-04       Impact factor: 3.847

Review 6.  Diffusion tensor imaging and fiber tractography in brain malformations.

Authors:  Andrea Poretti; Avner Meoded; Andrea Rossi; Charles Raybaud; Thierry A G M Huisman
Journal:  Pediatr Radiol       Date:  2013-01-04

7.  Ataxia, intellectual disability, and ocular apraxia with cerebellar cysts: a new disease?

Authors:  Andrea Poretti; Martin Häusler; Arpad von Moers; Bastian Baumgartner; Klaus Zerres; Andrea Klein; Chiara Aiello; Francesca Moro; Ginevra Zanni; Filippo M Santorelli; Thierry A G M Huisman; Joachim Weis; Enza Maria Valente; Enrico Bertini; Eugen Boltshauser
Journal:  Cerebellum       Date:  2014-02       Impact factor: 3.847

8.  Joubert syndrome.

Authors:  Lakshmikanth Halegubbi Karegowda; Poonam Mohan Shenoy; Smiti Sripathi; Mugil Varman
Journal:  BMJ Case Rep       Date:  2014-03-20

9.  An unusual association of classical Joubert syndrome with retrocerebellar arachnoid cyst.

Authors:  Sachin Baldawa
Journal:  Childs Nerv Syst       Date:  2016-05-02       Impact factor: 1.475

10.  Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy.

Authors:  Karina Tuz; Ruxandra Bachmann-Gagescu; Diana R O'Day; Kiet Hua; Christine R Isabella; Ian G Phelps; Allan E Stolarski; Brian J O'Roak; Jennifer C Dempsey; Charles Lourenco; Abdulrahman Alswaid; Carsten G Bönnemann; Livija Medne; Sheela Nampoothiri; Zornitza Stark; Richard J Leventer; Meral Topçu; Ali Cansu; Sujatha Jagadeesh; Stephen Done; Gisele E Ishak; Ian A Glass; Jay Shendure; Stephan C F Neuhauss; Chad R Haldeman-Englert; Dan Doherty; Russell J Ferland
Journal:  Am J Hum Genet       Date:  2013-12-19       Impact factor: 11.025

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