Affiliation:
1. Department of Medicine, The George Washington University School of Medicine and Health Sciences, Washington, D.C.
Abstract
The Holt-Oram syndrome is reported for the first time in a Puerto Rican family of one mother and two daughters. All had severe upper limb anomalies and secundum atrial septal defect. One daughter, the proband, had, in addition, a persistent left superior vena cava, a cardiac anomaly that has not been previ ously reported in association with the Holt-Oram syndrome.
Subject
Cardiology and Cardiovascular Medicine
Cited by
7 articles.
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