Literature DB >> 18810345

Tectocerebellar dysraphia and occipital encephalocele: an unusual association with abdominal situs inversus and congenital heart disease.

Sriram Krishnamurthy1, Seema Kapoor, Vipul Sharma, Anjali Prakash.   

Abstract

Tectocerebellar dysraphia is a rare constellation of malformations comprising of occipital encephalocele, aplasia of the cerebellar vermis and deformity of the tectum. We describe a 7 month old infant who presented with tectocerebellar dysraphia associated with double outlet right ventricle, pulmonary stenosis and abdominal situs inversus. This association has not been reported in the literature, to the best of our knowledge.

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Year:  2008        PMID: 18810345     DOI: 10.1007/s12098-008-0183-6

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  13 in total

Review 1.  Left-right asymmetry in vertebrate development.

Authors:  M L López-Gracia; M A Ros
Journal:  Adv Anat Embryol Cell Biol       Date:  2007       Impact factor: 1.231

2.  Clinical analysis of families with heart, midline, and laterality defects.

Authors:  S H Morelli; L Young; B Reid; H Ruttenberg; M J Bamshad
Journal:  Am J Med Genet       Date:  2001-07-15

3.  Evidence for the "midline" hypothesis in associated defects of laterality formation and multiple midline anomalies.

Authors:  E Gilbert-Barness; D Debich-Spicer; M M Cohen; J M Opitz
Journal:  Am J Med Genet       Date:  2001-07-15

4.  Syndromes identified in fetuses with prenatally diagnosed cephaloceles.

Authors:  S J Wininger; A E Donnenfeld
Journal:  Prenat Diagn       Date:  1994-09       Impact factor: 3.050

5.  The SIL gene is required for mouse embryonic axial development and left-right specification.

Authors:  S Izraeli; L A Lowe; V L Bertness; D J Good; D W Dorward; I R Kirsch; M R Kuehn
Journal:  Nature       Date:  1999-06-17       Impact factor: 49.962

Review 6.  Of mice and men: dissecting the genetic pathway that controls left-right asymmetry in mice and humans.

Authors:  H Schneider; M Brueckner
Journal:  Am J Med Genet       Date:  2000

7.  Uncommon syndromes of cerebellar vermis aplasia. II: Tecto-cerebellar dysraphia with occipital encephalocele.

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

8.  Node and midline defects are associated with left-right development in Delta1 mutant embryos.

Authors:  Gerhard K H Przemeck; Ulrich Heinzmann; Johannes Beckers; Martin Hrabé de Angelis
Journal:  Development       Date:  2003-01       Impact factor: 6.868

9.  Tecto-cerebellar dysraphia with occipital encephalocele.

Authors:  U M Chowdhary; A W Ibrahim; A S Ammar; A H Dawodu
Journal:  Surg Neurol       Date:  1989-04

10.  Tectocerebellar dysraphia with posterior encephalocele (Friede): report of the youngest case. Reappraisal of the condition uniting Cleland-Chiari (Arnold-Chiari) and Dandy-Walker syndromes.

Authors:  A Hori
Journal:  Clin Neuropathol       Date:  1994 Jul-Aug       Impact factor: 1.368

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  8 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

Review 2.  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

3.  A Rare Triad of Giant Occipital Encephalocele with Lipomyelomeningocele, Tetralogy of Fallot, and Situs Inversus.

Authors:  Arie Franco; Stephanie Y Jo; Amar S Mehta; Dave J Pandya; Carina W Yang
Journal:  J Radiol Case Rep       Date:  2016-03-31

4.  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

5.  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

6.  Tecto-cerebellar dysraphia manifesting as occipital meningocoele associated with congenital melanocytic nevi and pectus excavatum.

Authors:  Amit Agrawal; Sudhakar Ratanlal Joharapurkar; Ata-Ullah Khan
Journal:  Iran J Pediatr       Date:  2010-03       Impact factor: 0.364

7.  Purkinje cell compartmentation in the cerebellum of the lysosomal Acid phosphatase 2 mutant mouse (nax - naked-ataxia mutant mouse).

Authors:  Karen Bailey; Maryam Rahimi Balaei; Ashraf Mannan; Marc R Del Bigio; Hassan Marzban
Journal:  PLoS One       Date:  2014-04-10       Impact factor: 3.240

8.  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

  8 in total

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