Management of a DAVF in a Patient with Loeys-Dietz Syndrome Type II
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DOI: 10.1007/s00062-021-01007-3
Abstract: Loeys-Dietz syndrome (LDS) is a rare autosomal dominant connective tissue disease characterized by generalized arterial tortuosity with aneurysms and dissections in association with craniofacial and skeletal manifestations [1, 2]. Typical LDS patients have hypertelorism, bifid… read more here.
Keywords: patient loeys; management davf; davf patient; syndrome type ... See more keywords