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  - 2024/04/24
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164070806
ER  -