Erratum: Congenital mydriasis and prunebelly syndrome in a child with an ACTA2 mutation

Authors

Michael C. Brodsky, Mayo Clinic, United States
Kadriye Erkan Turan, Hacettepe University School of Medicine, Turkey
Cheryl L. Khanna, Mayo Clinic, United States
Alice Patton, Mayo Clinic, United States
Salman Kirmani, Mayo Clinic, United StatesFollow

Document Type

Report

Department

Paediatrics and Child Health

Abstract

We report the association of congenital mydriasis with prune belly syndrome and cerebrovascular anomalies in a 9-year-old boy who was found to have an ACTA2 mutation. This case illustrates the spectrum of systemic malformations that are attributable to mutations in ACTA2 and expands the spectrum of cerebrovascular anomalies that are now known to accompany congenital mydriasis.

Comments

This work was published before the author joined Aga Khan University.

Publication (Name of Journal)

Journal of American Association for Pediatric Ophthalmology and Strabismus

Recommended Citation

Brodsky, M. C., Turan, K. E., Khanna, C. L., Patton, A., Kirmani, S. (2014). Erratum: Congenital mydriasis and prunebelly syndrome in a child with an ACTA2 mutation. Journal of American Association for Pediatric Ophthalmology and Strabismus, 18(5), 518-518.
Available at: https://ecommons.aku.edu/pakistan_fhs_mc_women_childhealth_paediatr/1313