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V. Prazeres

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Open access Oct 2026

Congenital variant of Rett syndrome due to a mutation in the FOXG1 gene: a pediatric case report in Amazon

Case Presentation: A 2-year-old male patient, born at term at 38 weeks of gestation through vaginal delivery, with Apgar scores of 9/10, and born to non-consanguineous parents, started a condition with postnatal microcephaly, psychomotor agitation, daily seizures, and non-restorative sleep for approximately one year, a...

B. Aguiar, Mateus Nunes Horewicz, G. Traven et al. · 0 citations

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