VACTERL association is considered as a syndrome with a non-random combination of various developmental anomalies in one patient. A review of the scientific literature is presented. The clinical case is a patient with incomplete VACTERL association with predominant involvement of the skeletal system in combination with congenital hypoplasia of the right lung. The article reflects the experience of doctors in the diagnosis and treatment of this rare disease.
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Dubova et al. (2024) studied this question.
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