Abstract
Lipoid proteinosis (LP), also known as Urbach-Wiethe disease, is a rare autosomal recessive genodermatosis having multisystem syndromic involvement of skin, upper aerodigestive tract, internal organs, and eyelids. Although the ocular manifestations are rare, it is important to identify these clinical entities for early diagnosis and improved outcomes. We, hereby, describe a case of a 17-year-old female who presented with complaints of chronic itching and discomfort of both eyelids on and off.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have