Fatal leukodystrophy in Costello syndrome: a case report

Costello syndrome (CS) is a rare genetic condition characterized by dysregulation of the signaling pathway, phenotypic alteration due to fetal macrosomia or growth retardation, facial abnormalities, loose skin...

Source: BMC Pediatrics - July 24, 2023 Category: Pediatrics Authors: Virgilio E. Failoc-Rojas, Piero A. Quiroz Ugaz, Dante A. Loconi Le ón and Sandra Zeña-Ñañez Tags: Case report Source Type: research