Ophthalmologic and neuro‐ophthalmologic findings in children with Down syndrome

Author:

Jain Aarushi1,Boyd Natalie K.2,Paulsen Kelli C.2,Vogel Benjamin N.2,Nguyen Lina2,Santoro Jonathan D.23

Affiliation:

1. Boston University Boston Massachusetts USA

2. Division of Neurology, Department of Pediatrics Children's Hospital Los Angeles Los Angeles California USA

3. Department of Neurology Keck School of Medicine at the University of Southern California Los Angeles California USA

Abstract

AbstractDown syndrome, also known as Trisomy 21, is a genetic disorder associated with mild‐to‐moderate intellectual disability, delays in growth, and characteristic facial features. A wide range of ocular complications are seen in children with Down syndrome, including strabismus, nystagmus, refractive errors, congenital cataracts, the presence of keratoconus, and decreased visual acuity. Early ophthalmic examination is needed for early diagnosis and treatment in patients. This narrative review examines ocular manifestations in children with Down syndrome and the importance of prompt ophthalmic interventions for treatment.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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