Literature DB >> 21636654

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

I Harting1, U Kotzaeridou, A Poretti, A Seitz, J Pietz, M Bendszus, E Boltshauser.   

Abstract

The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a rare, most often autosomal-recessive disorder with a characteristic malformation of the midhindbrain. We describe 3 patients with JSRD and the additional MR finding of tissue resembling heterotopia in the interpeduncular fossa, which in one patient was combined with a more extensive intramesencephalic heterotopia. Interpeduncular heterotopia has not been reported previously, either in the context of JSRD or as a separate entity. This new imaging feature enlarges the spectrum of brain stem abnormalities in JSRD. In view of the underlying ciliopathy, it seems likely that the interpeduncular heterotopia results from misdirected migration.

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Year:  2011        PMID: 21636654      PMCID: PMC7966074          DOI: 10.3174/ajnr.A2488

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


  18 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.  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

3.  Prenatal and neonatal MR imaging findings in oral-facial-digital syndrome type VI.

Authors:  A Poretti; U Brehmer; I Scheer; V Bernet; E Boltshauser
Journal:  AJNR Am J Neuroradiol       Date:  2008-03-20       Impact factor: 3.825

4.  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

5.  Neuropathology of Joubert syndrome.

Authors:  A T Yachnis; L B Rorke
Journal:  J Child Neurol       Date:  1999-10       Impact factor: 1.987

6.  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

7.  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

8.  Joubert syndrome: a clinico-radiological study.

Authors:  B Kendall; D Kingsley; S R Lambert; D Taylor; P Finn
Journal:  Neuroradiology       Date:  1990       Impact factor: 2.804

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.  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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  7 in total

1.  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

2.  Decaying molar tooth sign in Joubert syndrome and related disorders is correlated to a displacement of the corticospinal tract.

Authors:  César Augusto Pinheiro Ferreira Alves; Suely Ferraciolli; Ciro Matsui; Leandro Tavares Lucato
Journal:  Neuroradiology       Date:  2017-10-28       Impact factor: 2.804

3.  Ahi1 promotes Arl13b ciliary recruitment, regulates Arl13b stability and is required for normal cell migration.

Authors:  Jesús Muñoz-Estrada; Russell J Ferland
Journal:  J Cell Sci       Date:  2019-09-04       Impact factor: 5.285

4.  Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.

Authors:  Andrea Poretti; Giuseppina Vitiello; Raoul C M Hennekam; Filippo Arrigoni; Enrico Bertini; Renato Borgatti; Francesco Brancati; Stefano D'Arrigo; Francesca Faravelli; Lucio Giordano; Thierry A G M Huisman; Miriam Iannicelli; Gerhard Kluger; Marten Kyllerman; Magnus Landgren; Melissa M Lees; Lorenzo Pinelli; Romina Romaniello; Ianina Scheer; Christoph E Schwarz; Ronen Spiegel; Daniel Tibussek; Enza Maria Valente; Eugen Boltshauser
Journal:  Orphanet J Rare Dis       Date:  2012-01-11       Impact factor: 4.123

5.  Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome.

Authors:  F Arrigoni; R Romaniello; D Peruzzo; A De Luca; C Parazzini; E M Valente; R Borgatti; F Triulzi
Journal:  AJNR Am J Neuroradiol       Date:  2017-08-24       Impact factor: 3.825

6.  Developmental disorders of the midbrain and hindbrain.

Authors:  A James Barkovich
Journal:  Front Neuroanat       Date:  2012-03-06       Impact factor: 3.856

7.  Validation of In utero Tractography of Human Fetal Commissural and Internal Capsule Fibers with Histological Structure Tensor Analysis.

Authors:  Christian Mitter; András Jakab; Peter C Brugger; Gerda Ricken; Gerlinde M Gruber; Dieter Bettelheim; Anke Scharrer; Georg Langs; Johannes A Hainfellner; Daniela Prayer; Gregor Kasprian
Journal:  Front Neuroanat       Date:  2015-12-24       Impact factor: 3.856

  7 in total

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