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Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family
BackgroundMacular corneal dystrophy (MCD) is a rare autosomal recessive disorder that is characterized by progressive corneal opacity that starts in early childhood and ultimately progresses toExpand
Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family
Purpose To report on a clinical and genetic investigation of a large, multigenerational South African family of mixed ancestry with autosomal dominant congenital cataracts, coloboma, and nystagmus.Expand
A 20-Year Retrospective Review of Retinoblastoma at Two Tertiary Academic Hospitals in Johannesburg, South Africa
Aim: This paper presents a 20-year review of retinoblastoma in Johannesburg, South Africa, aiming to better characterize the disease in this sub-Saharan setting. Methods: The study represents aExpand
GS19P
VERSAJET: A NOVEL APPROACH TO DEBRIDEMENT
The addition of hydrosurgery into our surgical armamentarium will aim to revolutionize surgical wound debridement. Hydrosurgery (Versajet 1 ) utilizes a high pressure fine saline jet delivered via aExpand
Retinoblastoma in South Africa - A 20-year retrospective study at two tertiary academic hospitals in Johannesburg
A dissertation submitted to the Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, in fulfillment of the requirements for the degree of Master of Medicine in Ophthalmology Expand