RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164075094
T1 Keratitis Ichthyosis Deafness (KID) Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164075094
RD 2024/09/12
AB It  is  a  rare  disease  associated  with  ectodermal  dysplasia  characterized  by  inflammation  of  the  corneae  (keratitis),  erythrokeratoderma,  skin  scaling  (ichthyosis)  especially  the  palms  of  the  hands  and  sole  of  the  feet,  and  sensorineural  deafness.