Crouzon Syndrome Associated with Congenital Coarctation of Aorta
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DOI: 10.4103/0366-6999.233963
Abstract: To the Editor: Crouzon Syndrome (CS), also known as craniosynostosis, is an autosomal dominant genetic disorder linked to single‐gene mutation of fibroblast growth factor receptor 2 (FGFR2).[1‐3] The premature fusion of certain skull bones results… read more here.
Keywords: syndrome associated; crouzon syndrome; congenital coarctation; associated congenital ... See more keywords