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Noonan syndrome or new autosomal dominant condition with coarctation of the aorta, hypertrophic cardiomyopathy, and minor anomalies

✍ Scribed by Lemire, Edmond G.


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
126 KB
Volume
113
Category
Article
ISSN
0148-7299

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✦ Synopsis


Abstract

This is a report on a father and his two children with an apparent autosomal dominant condition characterized by craniofacial anomalies, coarctation of the aorta, hypertrophic cardiomyopathy, and other structural heart abnormalities with normal psychomotor development. Some clinical features are reminiscent of Noonan syndrome. Alternatively, this family may have a previously undescribed genetic condition. The family history is suggestive of a new autosomal dominant mutation in the father. © 2002 Wiley‐Liss, Inc.