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Medically actionable comorbidities in adults with Costello syndrome

Authors :
K. Nicole Weaver
Karen W. Gripp
Amy R. Shikany
Deborah L. Stabley
Daniel Doyle
Katherine M. Robbins
Laura Baker
Source :
American Journal of Medical Genetics Part A. 182:130-136
Publication Year :
2019
Publisher :
Wiley, 2019.

Abstract

Costello syndrome (CS) is an autosomal-dominant condition caused by activating missense mutations in HRAS. There is little literature describing health concerns specific to adults with CS. Parents of individuals with CS need to know what to anticipate as their children age. We surveyed a group of 20 adults and older adolescents with CS regarding their medical concerns and lifestyle characteristics. We identified several previously undescribed actionable medical concerns in adults with CS. First, the high prevalence of anxiety in this cohort indicates that screening for anxiety is warranted since this is a treatable condition that can have a significant impact on quality of life. Second, adults with CS should be monitored for progressive contractures or other problems that could decrease mobility. This is especially important in a population that seems to have increased risk for osteopenia. Finally, the lack of cancer diagnoses in adulthood is of interest, although the cohort is too small to draw definitive conclusions about cancer risk in adults with CS. Ongoing follow-up of the current cohort of adults with CS is necessary to delineate progressive medical and physical problems, which is essential for providing targeted management recommendations and anticipatory guidance to families.

Details

ISSN :
15524833 and 15524825
Volume :
182
Database :
OpenAIRE
Journal :
American Journal of Medical Genetics Part A
Accession number :
edsair.doi.dedup.....3163b2912e803f4065e56556346bcb5a