Sindrome di Holt-Oram: valutazione cardiologica, radiologica e genetica.

Translated title of the contribution: Holt-Oram syndrome: cardiological, radiological and genetic evaluation

V. Donadeo, M. Solarino, O. Alfieri, C. Fucci, G. Guanti, F. Susca, G. Brindicci

Research output: Contribution to journalArticlepeer-review

Abstract

A case of a 63-year-old woman with Holt-Oram syndrome is presented. The patient, operated at 38 years for correction of an interatrial defect of the ostium secundum type presented with upper extremity skeletal abnormalities, in particular on the left, and a severe mitral insufficiency with ruptured chordae tendinae of the posterior leaflet. Mitral valve reconstruction was followed by an unusual severe hemolytic anemia and acute secondary renal insufficiency. Valve replacement was therefore necessary. At present, the patient, whose karyotype is normal, is in NYHA functional class I.

Translated title of the contributionHolt-Oram syndrome: cardiological, radiological and genetic evaluation
Original languageItalian
Pages (from-to)199-203
Number of pages5
JournalCardiologia
Volume40
Issue number3
Publication statusPublished - Mar 1995

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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