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

Patrizia D'Eufemia, Mauro Celli, Paolo Versacci, Anna Zambrano, Valentina Lodato, Pietro Persiani, Luca Sangiorgi

Research output: Contribution to journalArticlepeer-review


Cardiovascular involvement is relatively rare in osteogenesis imperfecta and has a predilection for left-sided cardiac valves. We report a 5 years old female child affected by osteogenesis imperfecta type I in which an asymptomatic mild form of Ebstein's anomaly, a congenital tricuspid malformation, was diagnosed during routinely investigation. The association of these two relatively rare entities could provide new insight to better understand the pathogenesis of cardiac involvement in osteogenesis imperfecta.

Original languageEnglish
Pages (from-to)50-51
Number of pages2
JournalClinical Cases in Mineral and Bone Metabolism
Issue number2
Publication statusPublished - May 2011


  • Collagen type I
  • Ebstein's anomaly
  • Osteogenesis imperfect
  • Valvular heart disease

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Internal Medicine


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