Author:
Ma Chu Jian,Oatts Julius T.,Indaram Maanasa
Abstract
The authors report a case of lacrimo-auriculo-dento-digital syndrome in a 16-month-old boy with punctal agenesis, upper canalicular dysgenesis and polydactyly, presenting as bilateral congenital nasolacrimal duct obstruction and unilateral acute dacryocystitis. Genetic sequencing revealed a novel mutation in fibroblast growth factor 10.
[
J Pediatr Ophthalmol Strabismus
. 2023;60(4):e38–e40.]
Subject
Ophthalmology,General Medicine,Pediatrics, Perinatology and Child Health