RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164070806 T1 Gillespie Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164070806 RD 2024/10/07 AB Inherited rare genetic polymalformative disorder characterized by nonprogressive partial aniridia (meaning that part of the iris is missing), ataxia, mental/intellectual deficiency, cerebellar ataxia, and gross incoordination. Characteristic appearance of the eyes in the first month is crucial in making the diagnosis.