Ocular Manifestations of Hutchinson-Gilford Progeria Syndrome: A Rare Presentation
June 2022
in “
Indian journal of clinical and experimental opthalmology
”
Hutchinson-Gilford Progeria Syndrome madarosis lagophthalmos dry eye keratinized ocular surface Meibomian gland dysfunction vascularized cornea symblepharon corneal opacification cataract hair loss scleroderma HGP eyebrow loss incomplete eyelid closure dry eyes keratinized eye surface Meibomian gland issues vascularized eye eyelid adhesion corneal clouding cataracts baldness skin hardening
Studysummary This case report details the ocular complications of Hutchinson-Gilford Progeria syndrome in a 20-year-old Bangladeshi patient, highlighting symptoms like dry eyes, Meibomian gland dysfunction, and cataracts.
Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
Read the full study on ijceo.org →