Ceroid storage disease: Difference between revisions

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==Overview==
==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.<ref>http://www.checkorphan.org/disease/ceroid-storage-disease</ref>
A rare [[metabolic]] storage disease characterized by abnormal deposits of a waxy substance called ceroid [[lipofuscin]] in various parts of the body such as the [[liver]], [[spleen]] and intestinal lining.<ref>http://www.checkorphan.org/disease/ceroid-storage-disease</ref>


==Natural History, Complications and Prognosis==
==Natural History, Complications and Prognosis==
* Liver [[cirrhosis]]
* Childhood death
* Childhood death
* Liver [[cirrhosis]]


==Diagnosis==
==Diagnosis==
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* [[Liver failure]]
* [[Liver failure]]
==Laboratory Findings==
==Laboratory Findings==
===Biopsy Findings===
* Ceroid deposits in the [[liver]]
* Ceroid deposits in the [[liver]]
* Ceroid deposits in the [[spleen]]
* Ceroid deposits in the [[spleen]]
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[[Category:Disease]]
[[Category:Disease]]
[[Category:Grammar]]

Latest revision as of 16:20, 30 July 2012

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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 lipofuscin in various parts of the body such as the liver, spleen and intestinal lining.[1]

Natural History, Complications and Prognosis

Diagnosis

Symptoms

Laboratory Findings

Biopsy Findings

References

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