Lutz Richner Landolt syndrome
Overview
A rare disorder involving kidney and biliary abnormalities.
Symptoms
* Neonatal jaundice * Failure to thrive * Recurrent infections * Low-set ears * Highly arched roof of mouth * Barrel chest * Club feet * Hypotonia * Intrahepatic biliary hyperplasia * Calcification of distal kidney tubules * Increased blood levels of bilirubin * Excess amino acids in urine * Metabolic acidosis * Excess protein in urine * Excess sugar in the urine
Prognosis
The 'prognosis' of Lutz-Richner-Landolt syndrome usually refers to the likely outcome of Lutz-Richner-Landolt syndrome. The prognosis of Lutz-Richner-Landolt syndrome may include the duration of Lutz-Richner-Landolt syndrome, chances of complications of Lutz-Richner-Landolt syndrome, probable outcomes, prospects for recovery, recovery period for Lutz-Richner-Landolt syndrome, survival rates, death rates, and other outcome possibilities in the overall prognosis of Lutz-Richner-Landolt syndrome. Naturally, such forecast issues are by their nature unpredictable.