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Since 1988, when Rogers first described a boy with anophthalmia associated with esophageal atresia, eight similar cases have been reported. These patients lend support to the hypothesis that this association of congenital anomalies constitutes a discrete entity, although the etiology is still unknown. We report a patient with this combination of malformations as well as a marked hypoplasia of the entire left half of the body.
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Messina et al. (2003) studied this question.
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