Literature DB >> 28838911

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

F Arrigoni1, R Romaniello2, D Peruzzo3, A De Luca3,4, C Parazzini5, E M Valente6,7, R Borgatti2, F Triulzi8.   

Abstract

In Joubert syndrome, the "molar tooth" sign can be associated with several additional supra- and infratentorial malformations. Here we report on 3 subjects (2 siblings, 8-14 years of age) with Joubert syndrome, showing an abnormal thick bulging of the anterior profile of the mesencephalon causing a complete obliteration of the interpeduncular fossa. DTI revealed that the abnormal tissue consisted of an ectopic white matter tract with a laterolateral transverse orientation. Tractographic reconstructions support the hypothesis of impaired axonal guidance mechanisms responsible for the malformation. The 2 siblings were compound heterozygous for 2 missense variants in the TMEM67 gene, while no mutations in a panel of 120 ciliary genes were detected in the third patient. The name "anterior mesencephalic cap dysplasia," referring to the peculiar aspect of the mesencephalon on sagittal MR imaging, is proposed for this new malformative feature.
© 2017 by American Journal of Neuroradiology.

Entities:  

Mesh:

Year:  2017        PMID: 28838911      PMCID: PMC5708532          DOI: 10.3174/ajnr.A5360

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


  38 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

2.  The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.

Authors:  Ursula M Smith; Mark Consugar; Louise J Tee; Brandy M McKee; Esther N Maina; Shelly Whelan; Neil V Morgan; Erin Goranson; Paul Gissen; Stacie Lilliquist; Irene A Aligianis; Christopher J Ward; Shanaz Pasha; Rachaneekorn Punyashthiti; Saghira Malik Sharif; Philip A Batman; Christopher P Bennett; C Geoffrey Woods; Carole McKeown; Martine Bucourt; Caroline A Miller; Phillip Cox; Lihadh Algazali; Richard C Trembath; Vicente E Torres; Tania Attie-Bitach; Deirdre A Kelly; Eamonn R Maher; Vincent H Gattone; Peter C Harris; Colin A Johnson
Journal:  Nat Genet       Date:  2006-01-15       Impact factor: 38.330

3.  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

4.  Ectopic peripontine arcuate fibres, a novel finding in pontine tegmental cap dysplasia.

Authors:  Matthan W A Caan; Peter G Barth; Jikke-Mien Niermeijer; Charles B Majoie; Bwee Tien Poll-The
Journal:  Eur J Paediatr Neurol       Date:  2014-01-11       Impact factor: 3.140

Review 5.  Tectonic gene mutations in patients with Joubert syndrome.

Authors:  Peter Huppke; Eike Wegener; Helena Böhrer-Rabel; Hanno J Bolz; Barbara Zoll; Jutta Gärtner; Carsten Bergmann
Journal:  Eur J Hum Genet       Date:  2014-08-13       Impact factor: 4.246

6.  Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome.

Authors:  Hajime Miyata; Mio Miyata; Eisaku Ohama
Journal:  Neuropathology       Date:  2013-12-09       Impact factor: 1.906

7.  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

8.  Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center.

Authors:  Thierry Vilboux; Daniel A Doherty; Ian A Glass; Melissa A Parisi; Ian G Phelps; Andrew R Cullinane; Wadih Zein; Brian P Brooks; Theo Heller; Ariane Soldatos; Neal L Oden; Deniz Yildirimli; Meghana Vemulapalli; James C Mullikin; May Christine V Malicdan; William A Gahl; Meral Gunay-Aygun
Journal:  Genet Med       Date:  2017-01-26       Impact factor: 8.822

9.  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

10.  Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes.

Authors:  Susanne Roosing; Marta Romani; Mala Isrie; Rasim Ozgur Rosti; Alessia Micalizzi; Damir Musaev; Tommaso Mazza; Lihadh Al-Gazali; Umut Altunoglu; Eugen Boltshauser; Stefano D'Arrigo; Bart De Keersmaecker; Hülya Kayserili; Sarah Brandenberger; Ichraf Kraoua; Paul R Mark; Trudy McKanna; Joachim Van Keirsbilck; Philippe Moerman; Andrea Poretti; Ratna Puri; Hilde Van Esch; Joseph G Gleeson; Enza Maria Valente
Journal:  J Med Genet       Date:  2016-05-06       Impact factor: 6.318

View more
  5 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.  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.  Characterizing White Matter Tract Organization in Polymicrogyria and Lissencephaly: A Multifiber Diffusion MRI Modeling and Tractography Study.

Authors:  F Arrigoni; D Peruzzo; S Mandelstam; G Amorosino; D Redaelli; R Romaniello; R Leventer; R Borgatti; M Seal; J Y-M Yang
Journal:  AJNR Am J Neuroradiol       Date:  2020-07-30       Impact factor: 3.825

Review 4.  Review of Ocular Manifestations of Joubert Syndrome.

Authors:  Stephanie F Wang; Tia J Kowal; Ke Ning; Euna B Koo; Albert Y Wu; Vinit B Mahajan; Yang Sun
Journal:  Genes (Basel)       Date:  2018-12-04       Impact factor: 4.096

5.  Novel compound heterozygous TMEM67 variants in a Vietnamese family with Joubert syndrome: a case report.

Authors:  Thi Phuong Hoa Bui; Ngoc Tu Nguyen; Van Doan Ngo; Hoai-Nghia Nguyen; Thi Thanh Ha Ly; Huy Duong Do; Minh-Tuan Huynh
Journal:  BMC Med Genet       Date:  2020-01-30       Impact factor: 2.103

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.