Literature DB >> 22576596

[Congenital heart defects of the septa, endocardial cushions and the conotruncus].

A M Müller1, N Sarioglu.   

Abstract

During embryological development the heart develops from a simple tube into a complex fully developed heart with four chambers. Hence all congenital heart defects develop before the ninth week of gestation. Currently a steadily increasing number of genetic mutations have been found to be responsible for congenital heart defects. Nevertheless, up to now it has been impossible to diagnose a heart defect just on the basis of molecular pathology. Despite the current excellent prenatal and postnatal ultrasound diagnostics, the post-mortem examination is still the gold standard for the diagnosis of complex heart malformations. However, this requires knowledge of the pathomorphology of the heart malformation in question. Therefore, characteristic and distinguishing features of septal defects including atrioventricular septal defects are presented, especially as the latter are part of complex heart defects, such as conotruncal heart malformations.

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Year:  2012        PMID: 22576596     DOI: 10.1007/s00292-011-1557-5

Source DB:  PubMed          Journal:  Pathologe        ISSN: 0172-8113            Impact factor:   1.011


  19 in total

1.  Chromosome 22q11 deletions in patients with conotruncal heart defects.

Authors:  A Khositseth; C Tocharoentanaphol; P Khowsathit; N Ruangdaraganon
Journal:  Pediatr Cardiol       Date:  2005 Sep-Oct       Impact factor: 1.655

Review 2.  Intermediate and complete forms of atrioventricular canal.

Authors:  J M Pearl; H Laks
Journal:  Semin Thorac Cardiovasc Surg       Date:  1997-01

3.  Creation of an atrial septal defect without thoracotomy. A palliative approach to complete transposition of the great arteries.

Authors:  W J Rashkind; W W Miller
Journal:  JAMA       Date:  1966-06-13       Impact factor: 56.272

4.  Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence.

Authors:  M C Digilio; B Casey; A Toscano; R Calabrò; G Pacileo; M Marasini; E Banaudi; A Giannotti; B Dallapiccola; B Marino
Journal:  Circulation       Date:  2001-12-04       Impact factor: 29.690

5.  The hypoplastic left heart syndrome with intact atrial septum: atrial morphology, pulmonary vascular histopathology and outcome.

Authors:  J Rychik; J J Rome; M H Collins; W M DeCampli; T L Spray
Journal:  J Am Coll Cardiol       Date:  1999-08       Impact factor: 24.094

6.  Double outlet right ventricle. Study of 27 cases.

Authors:  A H Cameron; F Acerete; M Quero; M C Castro
Journal:  Br Heart J       Date:  1976-11

7.  Anatomic observations on complete form of persistent common atrioventricular canal with special reference to atrioventricular valves.

Authors:  G Rastelli; J W Kirklin; J L Titus
Journal:  Mayo Clin Proc       Date:  1966-05       Impact factor: 7.616

8.  Morphology and classification of complete atrioventricular defects.

Authors:  G P Piccoli; J L Wilkinson; F J Macartney; L M Gerlis; R H Anderson
Journal:  Br Heart J       Date:  1979-12

9.  Long form of latent TGF-beta binding protein 1 (Ltbp1L) is essential for cardiac outflow tract septation and remodeling.

Authors:  Vesna Todorovic; David Frendewey; David E Gutstein; Yan Chen; Laina Freyer; Erin Finnegan; Fangyu Liu; Andrew Murphy; David Valenzuela; George Yancopoulos; Daniel B Rifkin
Journal:  Development       Date:  2007-09-05       Impact factor: 6.868

10.  Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta, and d-transposition of the great arteries.

Authors:  Christopher A Loffredo; Anand Chokkalingam; Anne M Sill; Joann A Boughman; Edward B Clark; Janet Scheel; Joel I Brenner
Journal:  Am J Med Genet A       Date:  2004-01-30       Impact factor: 2.802

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  3 in total

1.  Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic Tetralogy of Fallot and double outlet right ventricle in a Chinese Han population.

Authors:  Xiaomin Huang; Wenquan Niu; Zhen Zhang; Chunxia Zhou; Zhiwei Xu; Jinfen Liu; Zhaokang Su; Wenxiang Ding; Haibo Zhang
Journal:  Mol Biol Rep       Date:  2014-01-28       Impact factor: 2.316

2.  Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients.

Authors:  Tian Pu; Yang Liu; Rang Xu; Fen Li; Sun Chen; Kun Sun
Journal:  Mol Genet Genomics       Date:  2017-10-10       Impact factor: 3.291

3.  Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients.

Authors:  Xu Mengmeng; Xu Yuejuan; Chen Sun; Lu Yanan; Li Fen; Sun Kun
Journal:  BMC Med Genet       Date:  2020-05-07       Impact factor: 2.103

  3 in total

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