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Familial primary hypertrophic osteoarthropathy in association with congenital cardiac disease

Published online by Cambridge University Press:  15 August 2006

Solomon E. Levin ,
Jeffrey R. Harrisberg  and
Kenny Govendrageloo
Solomon E. Levin
Affiliation:
Division of Paediatric Cardiology, Johannesburg Hospital, Faculty of the Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
Jeffrey R. Harrisberg
Affiliation:
Division of Paediatric Cardiology, Johannesburg Hospital, Faculty of the Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
Kenny Govendrageloo
Affiliation:
Division of Paediatric Cardiology, Johannesburg Hospital, Faculty of the Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
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Abstract

It is rare to find congenital cardiac disease in association with familial primary hypertrophic osteoarthropathy. We have now encountered three siblings, two of whom had digital clubbing, patent arterial ducts and delayed closure of the cranial fontanels. The third infant was unusual in that there was no clubbing, or cranial abnormality, despite a small ventricular septal defect. To the best of our knowledge, this association has not previously been observed.

Keywords

Familial occurrencepatent ductus arteriosusarterial ductventricular septal defect
Type
Brief Report
Information
Cardiology in the Young , Volume 12 , Issue 3 , May 2002 , pp. 304 - 307
Copyright
2002 Cambridge University Press

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