Multidisciplinary Management of Costello Syndrome: Current Perspectives.
Ontology highlight
ABSTRACT: Costello syndrome (CS) is a rare neurodevelopmental disorder caused by germline mutations in HRAS. 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 strong impact on the quality of life, a multidisciplinary team is essential in the management of such a condition from infancy to adult age, to promptly address any detected issue and to develop appropriate personalized follow-up protocols and treatment strategies. With the present paper we aim to h
SUBMITTER: Leoni C
PROVIDER: S-EPMC9169840 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
ACCESS DATA