Retinal dystrophy in two boys with Costello syndrome due to the HRAS p.Gly13Cys mutation

Mary Ella M Pierpont, Mary Richards, W. Keith Engel, Nancy J. Mendelsohn, Carole G Summers

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

Features of Costello Syndrome, a systemic disorder caused by germline mutations in the proto-oncogene HRAS from the RAS/MAPK pathway, include failure-to-thrive, short stature, coarse facial features, cardiac defects including hypertrophic cardiomyopathy, intellectual disability, and predisposition to neoplasia. Two unrelated boys with Costello syndrome and an HRAS mutation (p.Gly13Cys) are presented with their ophthalmologic findings. Both had early symptoms of nystagmus, photophobia, and vision abnormalities. Fundus examination findings of retinal dystrophy were present at age 3 years. Both boys have abnormal electroretinograms with reduced or undetectable rod responses along with reduced cone responses consistent with rod-cone dystrophy. Our observations suggest that early ophthalmic examination and re-evaluations are indicated in children with Costello syndrome.

Original languageEnglish (US)
Pages (from-to)1342-1347
Number of pages6
JournalAmerican Journal of Medical Genetics, Part A
Volume173
Issue number5
DOIs
StatePublished - May 2017

Keywords

  • Costello syndrome
  • HRAS mutation
  • Retinal Dystrophy

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