Xylosylprotein 4-beta-galactosyltransferase (XGPT) deficiency: Difference between revisions

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Xylosylprotein 4-beta-galactosyltransferase deficiency is a variant of [[Ehlers-Danlos syndrome]]
Xylosylprotein 4-beta-galactosyltransferase deficiency is a variant of [[Ehlers-Danlos syndrome]]


==Pathophysiology==
This disease is caused by mutation in the [[gene]] encoding [[xylosylprotein 4-beta-galactosyltransferase]] which catalyzes the second glycosyl transfer reaction in the assembly of the dermatan sulfate chain leading to defective synthesis of proteodermatan sulfate (PDS) .




==Pathophysiology==
==Diagnosis==
 
This disease is caused by mutation in the [[gene]] encoding [[xylosylprotein 4-beta-galactosyltransferase]].

Revision as of 14:43, 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]

Synonyms and keywords: Ehler's Danlos syndrome - progeroid form

Overview

Xylosylprotein 4-beta-galactosyltransferase deficiency is a variant of Ehlers-Danlos syndrome

Pathophysiology

This disease is caused by mutation in the gene encoding xylosylprotein 4-beta-galactosyltransferase which catalyzes the second glycosyl transfer reaction in the assembly of the dermatan sulfate chain leading to defective synthesis of proteodermatan sulfate (PDS) .


Diagnosis