RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164082054
T1 Polycystic Kidney Disease (PKD)
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=1164082054
RD 2024/04/18
AB Genetic  disorder  defined  by  the  pathological  development  of  fluid-filled  cysts  throughout  the  kidneys  leading  to  organ  enlargement  and  chronic  kidney  disease.  The  morbidity  associated  with  the  most  common  forms,  autosomal  dominant  PKD  (ADPKD)  and  autosomal  recessive  PKD  (ARPKD),  is  mostly  limited  to  the  kidney  and  liver  and  extends  from  neonates  to  old  age.