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Ophthalmo-acromelic syndrome: report and review
1Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey. mtekin@hsc.vcu.edu
American Journal of Medical Genetics
|December 23, 1999
Abstract:
The ophthalmo-acromelic syndrome of Waardenburg is an autosomal recessive trait comprising eye malformations ranging from true anophthalmia to mild microphthalmia with acromelic malformations. Some 29 affected individuals have been reported since Waardenburg's first report in 1935 [Waardenburg et al., 1961]. We report on a new case with bilateral anophthalmia and typical limb malformations. The patient also was found to have interruption of the inferior vena cava with azygos continuation as an additional finding. The previous reports are reviewed to elucidate the spectrum of the syndrome.