An unusual cardiomelic syndrome |
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Authors: | R F Stratton N Koehler W R Morrow |
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Affiliation: | Department of Pediatrics, Wilford Hall USAF Medical Center, San Antonio, TX 78236-5300. |
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Abstract: | We report on a patient with pre- and postnatal growth retardation, bilateral symmetrical ulnar agenesis with monodactyly, atrial septal defect, two ventricular septal defects, Wolff-Parkinson-White conduction abnormality, and abnormal configuration of the pancreas. Although she had some facial features reminiscent of the Brachmann-de Lange syndrome, relatively normal head size and motor development indicate a distinct syndrome. |
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