Research Paper: 2019 Nau

Date Published : 05/22/2019

Summary: COL4A1 mutations in two infants with congenital cataracts and porencephaly: an ophthalmologic perspective

Abstract: COL4A1 mutations present with a spectrum of clinical phenotypes often involving the cerebrovascular and ophthalmic systems. We present 2 cases of COL4A1 mutations that presented with congenital cataracts and porencephaly. Both patients had posterior cortical cataracts and radiographically defined bilateral posterior lenticonus. Considering the long- term clinical implications of these mutations, posterior cortical cataracts, bilateral posterior lenticonus, and porencephaly should raise clinical suspicion for COL4A1 mutations.