Eccentrochondrodysplasia: Difference between revisions

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==Overview==
==Overview==
Eccentrochondrodysplasia is a rare inherited biochemical disorder.
Eccentrochondrodysplasia is a rare [[inherited]] biochemical disorder.


==Pathophysiology==
==Pathophysiology==

Revision as of 15:28, 27 July 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief:Raviteja Guddeti, M.B.B.S.[2]

Overview

Eccentrochondrodysplasia is a rare inherited biochemical disorder.

Pathophysiology

This disease is characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of certain enzymes needed to break it down.

Associated conditions

Eccentrochondrodysplasia is characterized by:


References


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