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...

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Main Authors: Virgilio E. Failoc-Rojas (Author), Piero A. Quiroz Ugaz (Author), Dante A. Loconi León (Author), Sandra Zeña-Ñañez (Author)
Format: Book
Published: BMC, 2023-07-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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