Rama Kalantri, K17273, Dr. Tamal Roy, Dr. Krishnapada Baidya, Dr. Ankita Agarwal
Ocular coloboma can be seen in isolation or in association with an impressive number of multi-system syndromes like mainly renal, cardiac, neurological and structural defects of the face, extremities and genitalia.
A 45-year old female patient presented to us with poor vision in her left eye since childhood. She had no systemic symptoms or obvious visible structural deformities and no such family history. On examination, she had typical iris and fundus coloboma (chorioretinal coloboma including optic nerve head inferiorly) in her left eye with situs inversus totalis (dextrocardia associated with complete transposition of all abdominal organs).
Using key words– situs inversus totalis, chorioretinal and optic nerve head coloboma in PubMed, Google and in literature, we found that no such case has been reported yet.