Ceroid storage disease
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Aditya Govindavarjhulla, M.B.B.S. [2]
Overview
A rare metabolic storage disease characterized by the abnormal deposits of a waxy substance called ceroid lipfuscin in various parts of the body such as the liver, spleen and intestinal lining.
Natural History, Complications and Prognosis
- Childhood death
- Liver Cirrhosis
Diagnosis
Symptoms
- Liver failure
References