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 2024/04/23
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.