Literature DB >> 1575461

The Chiari type I malformation in two monozygotic twins and first-degree relatives.

L J Stovner1, J Cappelen, G Nilsen, O Sjaastad.   

Abstract

The presence of the Chiari type I malformation in 2 adult monozygotic female twins, their mother, and possibly in 2 of their 4 daughters is reported. The diagnosis was made by magnetic resonance imaging and confirmed at the time of surgery in 1 twin. Monozygosity of the twins was proved by DNA typing. The disorder in the present family should probably be classified together with the autosomal dominant craniocervical malformations. Nongenetic factors also seem to be important because the twins were discordant for the extent of herniation of the cerebellar tonsils and the presence of syringomyelia.

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Year:  1992        PMID: 1575461     DOI: 10.1002/ana.410310213

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  11 in total

Review 1.  What differences exist in the appropriate treatment of congenital versus acquired adult Chiari type I malformation?

Authors:  César Ramón; Andrés Gonzáles-Mandly; Julio Pascual
Journal:  Curr Pain Headache Rep       Date:  2011-06

2.  Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.

Authors:  Anthony M Musolf; Winson S C Ho; Kyle A Long; Zhengping Zhuang; Davis P Argersinger; Haiming Sun; Bilal A Moiz; Claire L Simpson; Elena G Mendelevich; Enver I Bogdanov; Joan E Bailey-Wilson; John D Heiss
Journal:  Eur J Hum Genet       Date:  2019-06-21       Impact factor: 4.246

3.  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

4.  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

5.  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

Review 6.  Headache and Chiari I malformation: clinical presentation, diagnosis, and controversies in management.

Authors:  Frederick R Taylor; Mark V Larkins
Journal:  Curr Pain Headache Rep       Date:  2002-08

7.  Posterior cranial fossa dimensions in the Chiari I malformation: relation to pathogenesis and clinical presentation.

Authors:  L J Stovner; U Bergan; G Nilsen; O Sjaastad
Journal:  Neuroradiology       Date:  1993       Impact factor: 2.804

8.  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

9.  Chiari malformation type I: what information from the genetics?

Authors:  Valeria Capra; Michele Iacomino; Andrea Accogli; Marco Pavanello; Federico Zara; Armando Cama; Patrizia De Marco
Journal:  Childs Nerv Syst       Date:  2019-08-05       Impact factor: 1.475

10.  Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

Authors:  Christina A Markunas; Karen Soldano; Kaitlyn Dunlap; Heidi Cope; Edgar Asiimwe; Jeffrey Stajich; David Enterline; Gerald Grant; Herbert Fuchs; Simon G Gregory; Allison E Ashley-Koch
Journal:  PLoS One       Date:  2013-04-19       Impact factor: 3.240

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