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An unusual case of Holt-Oram syndrome
International Journal of Cardiology
|December 1, 1984
An unusual case of Holt-Oram syndrome with arachnodactyly, high arch palate, thoracic scoliosis and hypoplasia of the left radial artery is reported. The relevant literature is discussed and the importance of vascular hypoplasia in genesis and localization of the skeletal deformities of this syndrome is stressed.
An unusual case of Holt-Oram syndrome with arachnodactyly, high arch palate, thoracic scoliosis and hypoplasia of the left radial artery is reported. The relevant literature is discussed and the importance of vascular hypoplasia in genesis and localization of the skeletal deformities of this syndrome is stressed.