Nearly every cell in the human body carries tiny hair-like projections called cilia, and faults in the genes that build or maintain them can disrupt several organs at once — a category of disease known as ciliopathies. Bardet-Biedl Syndrome (BBS) is one such condition, and while vision loss features prominently, it exists alongside a much wider set of systemic issues that Zimbabwean families are typically already addressing with physicians back home before they contact us.
Because BBS involves so much of the body beyond the eyes, we keep our own evaluation tightly focused: existing records are reviewed in advance to understand the full systemic context, freeing up the in-person visit for the retinal testing and planning that requires equipment most local facilities don’t have.

Associate Professor, Vitreo-Retina Surgeon. 10+ Years Experience

Senior Consultant Ophthalmologist & Eye Surgeon· 26+ yrs experience

Consultant Ophthalmologist & Eye Surgeon, MD, DO .16+ Years Experience
“No — our evaluation and treatment stay strictly focused on the retinal component. Weight management and kidney function need continued care from the appropriate specialists, and we’re happy to share updates with that team.”
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Often, yes — central vision in BBS tends to be affected somewhat sooner than in non-syndromic RP, which is exactly why we recommend more frequent monitoring for these patients specifically.”
“Definitely. A baseline ERG and OCT before symptoms appear gives us a reference point that makes future changes far easier to catch, and allows us to plan low-vision support ahead of time rather than reacting later.”
“The complete picture is genuinely useful for understanding the syndrome as a whole, even though our hands-on evaluation during the visit will concentrate specifically on the retina.”
