Literature DB >> 7861232

Tonsillar ectopia and Chiari malformations: monozygotic triplets. Case report.

R K Cavender1, J H Schmidt.   

Abstract

A unique case of monozygotic triplets, each of whom exhibits variable degrees of tonsillar ectopia, is reported. Patient X presented with a Chiari I malformation and associated syringomyelia; examination of patients Y and Z showed 4 mm and 2.5 mm of tonsillar ectopia, respectively. No such case has been reported in the literature. The discussion defines the current magnetic resonance criteria for diagnosis of hindbrain malformations and addresses the question of whether these disorders represent a spectrum or separate disease entities, with specific emphasis on genetic predisposition. Due to the 100% concordance in this case the presence of a common hereditary factor in the etiology of these malformations is highly suggested.

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Year:  1995        PMID: 7861232     DOI: 10.3171/jns.1995.82.3.0497

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  12 in total

Review 1.  History, anatomic forms, and pathogenesis of Chiari I malformations.

Authors:  Edgardo Schijman
Journal:  Childs Nerv Syst       Date:  2004-02-05       Impact factor: 1.475

2.  Chiari I malformation and idiopathic growth hormone deficiency in siblings: report of three cases.

Authors:  R Lee Murphy; R Shane Tubbs; Paul A Grabb; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2007-05-30       Impact factor: 1.475

3.  Chiari I malformation and idiopathic growth hormone deficiency in siblings.

Authors:  R L Murphy; R S Tubbs; P A Grabb; W J Oakes
Journal:  Childs Nerv Syst       Date:  2006-01-18       Impact factor: 1.475

4.  Symptomatic tonsillar ectopia.

Authors:  K Furuya; K Sano; H Segawa; K Ide; H Yoneyama
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-02       Impact factor: 10.154

5.  Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics.

Authors:  Marcy C Speer; David S Enterline; Lorraine Mehltretter; Preston Hammock; Judith Joseph; Margaret Dickerson; Richard G Ellenbogen; Thomas H Milhorat; Michael A Hauser; Timothy M George
Journal:  J Genet Couns       Date:  2003-08       Impact factor: 2.537

6.  Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.

Authors:  Christina A Markunas; R Shane Tubbs; Roham Moftakhar; Allison E Ashley-Koch; Simon G Gregory; W Jerry Oakes; Marcy C Speer; Bermans J Iskandar
Journal:  J Neurosurg Pediatr       Date:  2012-04       Impact factor: 2.375

7.  Familial Chiari type I malformation with syringomyelia in two siblings: case report and review of the literature.

Authors:  Gaurav G Mavinkurve; Daniel Sciubba; Eric Amundson; George I Jallo
Journal:  Childs Nerv Syst       Date:  2005-04-09       Impact factor: 1.475

8.  Evolution of tonsillar ectopia associated with frontal encephalocoele.

Authors:  Dharmendra Ganesan; Richard D Hayward; Dominic N Thompson
Journal:  Childs Nerv Syst       Date:  2009-02-24       Impact factor: 1.475

9.  Chiari malformation type I associated with familial spastic paraplegia: report of a surgically treated case.

Authors:  A Fujimoto; A Matsumura; K Nakamura; T Aoki; T Enomoto
Journal:  Childs Nerv Syst       Date:  2004-09-28       Impact factor: 1.475

10.  Association of Chiari malformation and vitamin B12 deficit in a family.

Authors:  Melanie Welsch; Sebastian Antes; Michael Kiefer; Sascha Meyer; Regina Eymann
Journal:  Childs Nerv Syst       Date:  2013-03-07       Impact factor: 1.475

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