Literature DB >> 1409141

Osteogenesis imperfecta and Ebstein's anomaly: a case report with autopsy findings.

Y Warshaver1, C Bearer, D A Belchis.   

Abstract

Osteogenesis imperfecta is an inherited disorder of collagen synthesis. It has a wide range of phenotypic expressions, but cardiovascular anomalies tend to be rare. When they do occur, they usually consist of aortic or mitral valve disease. We report an autopsy case of a 36-week gestation infant with coexisting osteogenesis imperfecta and Ebstein's anomaly. The simultaneous occurrence of two relatively rare entities may reflect a generalized expression of an underlying collagen synthesis defect.

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Year:  1992        PMID: 1409141     DOI: 10.3109/15513819209023321

Source DB:  PubMed          Journal:  Pediatr Pathol        ISSN: 0277-0938


  1 in total

1.  Ebstein's anomaly in a child with osteogenesis imperfecta type I.

Authors:  Patrizia D'Eufemia; Mauro Celli; Paolo Versacci; Anna Zambrano; Valentina Lodato; Pietro Persiani; Luca Sangiorgi
Journal:  Clin Cases Miner Bone Metab       Date:  2011-05
  1 in total

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