TY - CHAP M1 - Book, Section TI - Gillespie Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/04 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164070806 ER -