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- W2291873306 abstract "Apert syndrome is an autosomal dominant disorder characterized by craniosynostosis, midfacial malformations and symmetric syndactyly of hands and feet. We present a case of a female Caucasian, 45 years old, prenatal diagnosis at 24 weeks gestation, apert syndrome type I, after sonography showing features deformity were observed characteristics. She refered pain at the fi rst head of the fi rst metatarsal of the left foot, long evolution that improves with rest and with the intake of oral analgesics, which is the realization of orthopedic treatment palie that the disease process." @default.
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- W2291873306 date "2011-01-01" @default.
- W2291873306 modified "2023-09-24" @default.
- W2291873306 title "Síndrome de Apert: tratamiento ortopédico Apert Syndrome: orthopedic treatment" @default.
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