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Gordon syndrome: literature review and a report of two cases.

Journal:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association


Issue Date:
2015


Abstract(summary):

The aim of this article is to publish a literature review and report on two new cases of Gordon syndrome (GS), a rare syndrome documented to have an autosomal dominant inheritance pattern or to occur sporadically; it is characterized by camptodactyly, cleft palate, and talipes equinovarus. We report two exceptional cases of GS where both patients were also diagnosed with congenital myopathy, and one developed malignant hyperthermia. These are the first two cases reported where patients were diagnosed with both GS and congenital myopathy or where GS is associated with malignant hyperthermia. =20


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