A case of Heterozygous mutation

A 56 found to have a heterozygous mutation (Arg149Cys) in ACTA2. Bilateral iris flocculi were recognized at the pupillary margin. Some of these were found to be collapsed. Iris atrophy and depigmentation were also observed. Fundus examinations showed no abnormalities. Can we discuss this condition? (It's not my case)


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It's IRIS FLOCCULI DIFFERENTIAL DIAGNOSIS Iris melanoma Iris posterior pigment hyperplasia Ectropion uvea Ciliary body tumour