NELSON CARLOS REİS FİLHO THAYS KAROLYNE PONTE PRADO AGUİAR DAFNİN LİMA SOUZA RAMOS BRUNA MARİAH MARTİNS MÜLLER ISADORA SOUSA OLİVEİRA FELİPE AUGUSTO CERNİ MANUELA BERTO PUCCA
Trends in Pediatrics - 2024;5(2):38-42
Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic condition characterized by premature aging resulting from an autosomal mutation in the LMNA gene. This article presents a groundbreaking instance of the first female monozygotic twins affected by HGPS, originating from Brazil, highlighting the exceptional nature of this case.
