Literature DB >> 11293748

Noncompaction of the myocardium associated with Roifman syndrome.

K Mandel1, E Grunebaum, L Benson.   

Abstract

Noncompaction of the ventricular myocardium, sometimes referred to as "spongy myocardium", appears as excessive and prominent trabeculations and deep intratrabecular recesses within the ventricular wall, usually involving the left ventricle, although the right ventricle and interventricular septum can also be affected. It may occur with or without additional heart malformations. Roifman syndrome is a constellation of antibody deficiency, spondyloepiphyseal dysplasia, facial dysmorphism, growth retardation, and retinal dystrophy. We report a patient with Roifman syndrome who presented with noncompaction of the left ventricular myocardium. Our findings expand the spectrum of diseases associated with noncompaction. The recognition of noncompaction among patients with Roifman syndrome is important, as the immune deficiencies may be subtle and undiagnosed until adulthood. Thus, some patients may first present with cardiac failure.

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Year:  2001        PMID: 11293748     DOI: 10.1017/s1047951101000208

Source DB:  PubMed          Journal:  Cardiol Young        ISSN: 1047-9511            Impact factor:   1.093


  10 in total

1.  Around PediHeart: noncompaction of the left ventricle.

Authors:  F McCaffrey
Journal:  Pediatr Cardiol       Date:  2001 Sep-Oct       Impact factor: 1.655

2.  Implications of genetic testing in noncompaction/hypertrabeculation.

Authors:  Joseph T C Shieh
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-07-10       Impact factor: 3.908

Review 3.  Left Ventricular Non-compaction: Is It Genetic?

Authors:  Teck Wah Ting; Saumya Shekhar Jamuar; Maggie Siewyan Brett; Ee Shien Tan; Breana Wen Min Cham; Jiin Ying Lim; Hai Yang Law; Ene Choo Tan; Jonathan Tze Liang Choo; Angeline Hwei Meeng Lai
Journal:  Pediatr Cardiol       Date:  2015-06-25       Impact factor: 1.655

Review 4.  Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction.

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

5.  Left ventricular noncompaction cardiomyopathy in association with trisomy 13.

Authors:  C J McMahon; A C Chang; R H Pignatelli; W C Miller-Hance; B K Eble; J A Towbin; S W Denfield
Journal:  Pediatr Cardiol       Date:  2005 Jul-Aug       Impact factor: 1.655

Review 6.  Primary noncompaction of the ventricular myocardium from the morphogenetic standpoint.

Authors:  U Bartram; J Bauer; D Schranz
Journal:  Pediatr Cardiol       Date:  2007-07-12       Impact factor: 1.838

7.  Non-compaction of the ventricular myocardium.

Authors:  Enrico Vizzardi; Savina Nodari; Marco Metra; Livio Dei Cas
Journal:  Heart Int       Date:  2006-12-15

8.  A homozygous mutation in the stem II domain of RNU4ATAC causes typical Roifman syndrome.

Authors:  Yael Dinur Schejter; Adi Ovadia; Roumiana Alexandrova; Bhooma Thiruvahindrapuram; Sergio L Pereira; David E Manson; Ajoy Vincent; Daniele Merico; Chaim M Roifman
Journal:  NPJ Genom Med       Date:  2017-07-10       Impact factor: 8.617

9.  Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing.

Authors:  Daniele Merico; Maian Roifman; Ulrich Braunschweig; Ryan K C Yuen; Roumiana Alexandrova; Andrea Bates; Brenda Reid; Thomas Nalpathamkalam; Zhuozhi Wang; Bhooma Thiruvahindrapuram; Paul Gray; Alyson Kakakios; Jane Peake; Stephanie Hogarth; David Manson; Raymond Buncic; Sergio L Pereira; Jo-Anne Herbrick; Benjamin J Blencowe; Chaim M Roifman; Stephen W Scherer
Journal:  Nat Commun       Date:  2015-11-02       Impact factor: 14.919

10.  Extending the critical regions for mutations in the non-coding gene RNU4ATAC in another patient with Roifman Syndrome.

Authors:  Ariane Hallermayr; Janine Graf; Udo Koehler; Andreas Laner; Brigitte Schönfeld; Anna Benet-Pagès; Elke Holinski-Feder
Journal:  Clin Case Rep       Date:  2018-10-11
  10 in total

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