Literature DB >> 20445194

Tectocerebellar dysraphism with vermian encephalocele.

Ihsan Anik1, Kenan Koc, Yonca Anik, Demir Kursat Yildiz, Savas Ceylan.   

Abstract

Tectocerebellar dysraphism is a very rare malformation associated with encephalocele and tectal deformity. This article presents tectocerebellar dysraphism with a solely vermian content of encephalocele and tectal beaking defined by magnetic resonance imaging (MRI) in a 5-month-old girl who was successfully treated surgically and demonstrated excellent prognosis at the 4-year follow-up.

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Year:  2010        PMID： 20445194     DOI： 10.1177/0883073810367828

Source DB:  PubMed          Journal:  J Child Neurol        ISSN： 0883-0738            Impact factor:   1.987


  4 in total

1.  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

2.  Tectocerebellar dysraphia with occipital encephalocele: a phenotypic variant of the TMEM231 gene mutation induced Joubert syndrome.

Authors:  Manal Nicolas-Jilwan; Ahmed Nasser Al-Ahmari; Mohammed Abdulaziz Alowain; Khaled Saleh Altuhaini; Essam Abdulaziz Alshail
Journal:  Childs Nerv Syst       Date:  2019-01-07       Impact factor: 1.475

3.  Prenatal Diagnosis of Tectocerebellar Dysraphia with Occipital Encephalocele.

Authors:  Hakan Timur; Cem Y Sanhal; Aytekin Tokmak; Kamil H Müftüoglu; Nuri Danisman
Journal:  J Clin Diagn Res       Date:  2015-12-01

4.  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
  4 in total

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