Article
Singleton-Merten syndrome: an autosomal dominant disorder with variable expression.
American journal of medical genetics. Part A - 1 Feb 2013
Feigenbaum Annette, Müller Christine, Yale Christopher, Kleinheinz Johannes, Jezewski Peter, Kehl Hans Gerd, MacDougall Mary, Rutsch Frank, Hennekam Raoul C M
Abstract excerpt
In 1973, Singleton and Merten described two females with abnormal dentition, unique radiographic changes especially of the hands, and severe calcification and intimal weakening of the aortic arch and valve. Since then three additional cases with similar features have been reported and the diagnos...
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