Literature DB >> 3890511

Upper limb malformations associated with congenital heart disease.

A E Lin, J K Perloff.   

Abstract

Upper limb malformations occur in patients with congenital heart disease as multifactorial, chromosomal or teratogenic combinations, and can be predictable (nonrandom) or sporadic (random) associations. The cardiac and limb defects represent either essential features of a syndrome or less common or less significant components. A practical classification is proposed based on the frequency and relative consistency of upper limb and cardiac associations. Recognition of upper limb malformations helps to identify accompanying cardiac disease and aids in the choice of diagnostic and therapeutic interventions in determination of prognosis and in genetic counseling. Upper limb malformations are the commonest skeletal abnormalities in patients with congenital heart disease, but it is also important to know with which limb defects concordance is low.

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Year:  1985        PMID: 3890511     DOI: 10.1016/0002-9149(85)90976-2

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  2 in total

1.  Holt-oram syndrome associated with double outlet right ventricle: A rare association.

Authors:  Bhupinder Singh; Mallesh Kariyappa; Ishwarappa Balekundri Vijayalakshmi; Manjunath C Nanjappa
Journal:  Ann Pediatr Cardiol       Date:  2013-01

2.  Holt-Oram Syndrome Associated with Aortic Atresia: A Rare Association.

Authors:  Sunil B Rodagi; Snehal S Surana; Vijaykumar R Potdar; Sharanbasav S Kirdi
Journal:  Heart Views       Date:  2016 Jan-Mar
  2 in total

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