Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Costello Syndrome

"Costello Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

Rare congenital disorder with multiple anomalies including: characteristic dysmorphic craniofacial features, musculoskeletal abnormalities, neurocognitive delay, and high prevalence of cancer. Germline mutations in H-Ras protein can cause Costello syndrome. Costello syndrome shows early phenotypic overlap with other disorders that involve MAP KINASE SIGNALING SYSTEM (e.g., NOONAN SYNDROME and cardiofaciocutaneous syndrome).


This graph shows the total number of publications written about "Costello Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Costello Syndrome" was a major or minor topic of these publication.
Bar chart showing 11 publications over 8 distinct years, with a maximum of 2 publications in 2011 and 2012 and 2018
To see the data from this visualization as text, click here.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.