Ceroid storage disease: Difference between revisions
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===Symptoms=== | ===Symptoms=== | ||
* [[Liver failure]] | * [[Liver failure]] | ||
==Laboratory Findings== | |||
* Ceroid deposits in [[liver]] | * Ceroid deposits in the [[liver]] | ||
* Ceroid deposits in [[spleen]] | * Ceroid deposits in the [[spleen]] | ||
* Ceroid deposits in [[intestinal]] lining | * Ceroid deposits in the [[intestinal]] lining | ||
==References== | ==References== | ||
Revision as of 15:15, 30 July 2012
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 abnormal deposits of a waxy substance called ceroid lipfuscin in various parts of the body such as the liver, spleen and intestinal lining.[1]
Natural History, Complications and Prognosis
- Childhood death
- Liver cirrhosis
Diagnosis
Symptoms
Laboratory Findings
- Ceroid deposits in the liver
- Ceroid deposits in the spleen
- Ceroid deposits in the intestinal lining