Ontology highlight
ABSTRACT:
SUBMITTER: Leoni C
PROVIDER: S-EPMC9169840 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
Leoni Chiara C Viscogliosi Germana G Tartaglia Marco M Aoki Yoko Y Zampino Giuseppe G
Journal of multidisciplinary healthcare 20220602
Costello syndrome (CS) is a rare neurodevelopmental disorder caused by germline mutations in <i>HRAS</i>. It belongs among the RASopathies, a group of syndromes characterized by alterations in components of the RAS/MAPK signaling pathway and sharing overlapping phenotypes. Its typical features include a distinctive facial appearance, growth delay, intellectual disability, ectodermal, cardiac, and musculoskeletal abnormalities, and cancer predisposition. Due to the several comorbidities having a ...[more]