Mucopolysaccharidosis Type IV

Common Name(s)

Mucopolysaccharidosis Type IV

Description for this condition is not yet available.
 

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Condition Specific Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Mucopolysaccharidosis Type IV" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Mucopolysaccharidosis Type IV" returned 2 free, full-text research articles on human participants. First 3 results:

Echocardiographic abnormalities in type IV mucopolysaccharidosis.
 

Author(s): R M John, D Hunter, R H Swanton

Journal: Arch. Dis. Child.. 1990 Jul;65(7):746-9.

 

Cardiac involvement is well recognised in most forms of the mucopolysaccharidoses but there is poor documentation of abnormalities specific to Morquio's syndrome (type IV mucopolysaccharidosis). Ten patients with the classic form or type A Morquio's syndrome with a median age of 12.5 ...

Last Updated: 14 Sep 1990

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Mucopolysaccharidosis type IV as a cause of mitral stenosis in an adult.
 

Author(s): M A Ireland, D B Rowlands

Journal: Br Heart J. 1981 Jul;46(1):113-5.

 

Last Updated: 22 Nov 1981

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Mucopolysaccharidosis Type IV" returned 1 free, full-text review articles on human participants. First 3 results:

[Morquio disease (Mucopolysaccharidosis type IV-A): clinical aspects, diagnosis and new treatment with enzyme replacement therapy].
 

Author(s): Juan Politei, Andrea B Schenone, Norberto Guelbert, Alejandro Fainboim, Marina Szlago

Journal: Arch Argent Pediatr. 2015 Aug;113(4):359-64.

 

Mucopolysaccharidosis type IV-A (Morquio A disease) is an autosomal recessive lysosomal storage disease caused by mutations in the gene encoding the N-acetylgalactosamine-6-sulfate sulfatase, that results in impaired catabolism of two glycosaminoglycans, chondroitin-6-sulfate and ...

Last Updated: 15 Jul 2015

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Biomarker for Morquio Disease
 

Status: Recruiting

Condition Summary: Lysosomal Storage Diseases; Morquio Disease

 

Last Updated: 25 Apr 2017

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Pregnancy With Morquio Syndrome - What Are Patients' Perspectives and Has ERT Changed Them?
 

Status: Recruiting

Condition Summary: Morquio Disease; MPS - Mucopolysaccharidosis

 

Last Updated: 10 May 2017

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Natural History of Atypical Morquio A Disease
 

Status: Not yet recruiting

Condition Summary: Mucopolysaccharidosis IV A

 

Last Updated: 29 Jun 2017

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