Literature DB >> 9462624

Interrupted inferior vena cava in asplenia syndrome and a review of the hereditary patterns of visceral situs abnormalities.

M Ruscazio1, S Van Praagh, A R Marrass, G Catani, S Iliceto, R Van Praagh.   

Abstract

We present the clinical and postmortem findings of the first photographically documented case of asplenia and interrupted inferior vena cava and the anatomic findings of 5 previously reported cases. A brief review of the various hereditary patterns of visceral situs abnormalities suggests that, at least in some cases, the asplenia and polysplenia syndromes are etiologically and pathogenetically interrelated.

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Year:  1998        PMID: 9462624     DOI: 10.1016/s0002-9149(97)00811-4

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


  2 in total

1.  Heterotaxy syndrome: defining contemporary disease trends.

Authors:  Terence W Prendiville; Leslie L Barton; William R Thompson; Doran L Fink; Kathryn W Holmes
Journal:  Pediatr Cardiol       Date:  2010-08-21       Impact factor: 1.655

2.  An unusual case of uninterrupted inferior vena cava with accessory hemizygous channel: An incidental finding in a child.

Authors:  Gaurav Agrawal; Anupam Das; Gaurav Gupta
Journal:  Ann Card Anaesth       Date:  2020 Oct-Dec
  2 in total

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