Araz, CoskunKaval, EbruTorgay, AdnanMoray, GokhanHaberal, Mehmet2024-02-122024-02-1220151304-0855http://hdl.handle.net/11727/11476Noonan syndrome is a congenital, common, hereditary disorder. Facial dysmorphism, growth retardation, and various heart defects are typical clinical features. In patients with minor cardiac pathology, life expectancy is normal. We report a case of renal transplant in a pediatric patient with Noonan syndrome that ended with death of the patient. Our patient presented with unexpected and refractory postoperative neurological complications that were unresponsive to intensive therapy, and the patient died because of secondary complications.enginfo:eu-repo/semantics/closedAccessAnesthesiaComplicationEnd-stage renal diseaseGeneticsarticle13Supplement 12732750003550584000552-s2.0-84939792898