Aniridia Differential Diagnosis

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blondemed

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Hi all,

I'm a CC3 putting together a case presentation on hereditary aniridia. A differential diagnosis is required. In this case both mother & son had no other abnormalities (MR, GU issues, Wilm's) but for the sake of educating my classmates I would like to include a broad differential - so far I've thought of coloboma, isolated iris hypoplasia, aniridia (congenital/ sporadic/wilm's associated), WAGR (Miller) syndrome, AGR syndrome, Rieger syndrome, Gillepsie syndrome ... what am I missing?

Thanks,
Blondemed

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