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Fatal leukodystrophy in Costello syndrome: a case report

Abstract Background 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, cardiovascular abnormalities, and a variable degree of intellectual d...

Whakaahuatanga katoa

I tiakina i:
Ngā taipitopito rārangi puna kōrero
Ngā kaituhi matua: Virgilio E. Failoc-Rojas, Piero A. Quiroz Ugaz, Dante A. Loconi León, Sandra Zeña-Ñañez
Hōputu: Artigo
Reo:Inglês
I whakaputaina: BMC 2023-07-01
Rangatū:BMC Pediatrics
Ngā marau:
Urunga tuihono:https://doi.org/10.1186/s12887-023-04166-z
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