Literature DB >> 15172004

Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12.

Alexander B Kenton1, Ximena Sanchez, Karen J Coveler, Kimberly A Makar, Shinawe Jimenez, Fukiko Ichida, Ross T Murphy, Perry M Elliott, William McKenna, Neil E Bowles, Jeffrey A Towbin, Karla R Bowles.   

Abstract

Isolated left ventricular noncompaction (LVNC) is a form of cardiomyopathy that most commonly presents in infancy with a hypertrophic and dilated left ventricle characterized by deep trabeculations and intertrabecular recesses. Our goal was to determine the frequency of mutations in G4.5, alpha-dystrobrevin, and FK Binding protein-12 in isolated LVNC patients. No mutations were identified in 47 of the 48 patients studied, while a splice site acceptor site mutation of intron 10 of G4.5 was identified in one patient, resulting in the deletion of exon 10 from the mRNA.

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Year:  2004        PMID: 15172004     DOI: 10.1016/j.ymgme.2004.02.009

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  21 in total

Review 1.  Isolated non-compaction cardiomyopathy.

Authors:  Rolf Engberding; Claudia Stöllberger; Peter Ong; Talat M Yelbuz; Birgit J Gerecke; Günter Breithardt
Journal:  Dtsch Arztebl Int       Date:  2010-03-26       Impact factor: 5.594

Review 2.  Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all.

Authors:  Thomas E Callis; Brian C Jensen; Karen E Weck; Monte S Willis
Journal:  Expert Rev Mol Diagn       Date:  2010-04       Impact factor: 5.225

3.  Isolated myocardial non-compaction in an infant with distal 4q trisomy and distal 1q monosomy.

Authors:  Gabriella De Rosa; Manuela Pardeo; Serena Bria; Elena Caresta; Isabella Vasta; Giuseppe Zampino; Marcella Zollino; Antonio Alberto Zuppa; Marco Piastra
Journal:  Eur J Pediatr       Date:  2005-01-22       Impact factor: 3.183

4.  Left-ventricular noncompaction in an infant with trisomy 21.

Authors:  Mandar B Patil; Sunita M Patil
Journal:  Pediatr Cardiol       Date:  2012-05-04       Impact factor: 1.655

5.  The prognostic role of CMR using global planimetric criteria in patients with excessive left ventricular trabeculation.

Authors:  Francesca Macaione; Antonella Meloni; Vincenzo Positano; Andrea Barison; Giancarlo Todiere; Laura Pistoia; Daniela Di Lisi; Giuseppina Novo; Salvatore Novo; Alessia Pepe
Journal:  Eur Radiol       Date:  2021-04-05       Impact factor: 5.315

6.  PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction.

Authors:  Emad Muhammad; Aviva Levitas; Sonia R Singh; Alex Braiman; Rivka Ofir; Sharon Etzion; Val C Sheffield; Yoram Etzion; Lucie Carrier; Ruti Parvari
Journal:  Hum Mol Genet       Date:  2015-10-12       Impact factor: 6.150

7.  The TNNI3 Arg192His mutation in a 13-year-old girl with left ventricular noncompaction.

Authors:  Mitsuhiro Fujino; Etsuko Tsuda; Keiichi Hirono; Masanori Nakata; Fukiko Ichida; Yukiko Hata; Naoki Nishida; Kenichi Kurosaki
Journal:  J Cardiol Cases       Date:  2018-07-01

Review 8.  Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction.

Authors:  Josef Finsterer
Journal:  Pediatr Cardiol       Date:  2009-01-29       Impact factor: 1.655

9.  [Isolated noncompaction cardiomyopathy with special emphasis on arrhythmia complications].

Authors:  B Gerecke; R Engberding
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2012-09-25

Review 10.  Genetic heterogeneity of left-ventricular noncompaction cardiomyopathy.

Authors:  Ewa Moric-Janiszewska; Grazyna Markiewicz-Łoskot
Journal:  Clin Cardiol       Date:  2008-05       Impact factor: 2.882

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