Hartnup Disease

Common Name(s)

Hartnup Disease

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hartnup Disease" 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 "Hartnup Disease" returned 21 free, full-text research articles on human participants. First 3 results:

Severe persistent unremitting dermatitis, chronic diarrhea and hypoalbuminemia in a child; Hartnup disease in setting of celiac disease.
 

Author(s): Thomas Ciecierega, Imad Dweikat, Mohammad Awar, Maher Shahrour, Bassam Abu Libdeh, Mutaz Sultan

Journal:

 

Celiac disease (CD) is a complex autoimmune disorder that can lead to an inflammatory small intestinal villous atrophy and malabsorption. Hartnup disease is an autosomal recessive disorder caused by increased urinary excretion of neutral amino acids. Co-occurrence of Hartnup disease ...

Last Updated: 27 Apr 2015

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Hartnup disease masked by kwashiorkor.
 

Author(s): Zerrin Orbak, Vildan Ertekin, Ayse Selimoglu, Nebahat Yilmaz, Huseyin Tan, Murat Konak

Journal: J Health Popul Nutr. 2010 Aug;28(4):413-5.

 

This report describes an 11-month old girl with Hartnup disease presenting with kwashiorkor and acrodermatitis enteropathica-like skin lesions but free of other clinical findings. This case with kwashiorkor had acrodermatitis enteropathica-like desquamative skin eruption. Since zinc ...

Last Updated: 9 Sep 2010

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Persistence of the common Hartnup disease D173N allele in populations of European origin.
 

Author(s): Dimitar N Azmanov, Helen Rodgers, Christiane Auray-Blais, Robert Giguère, Charles Bailey, Stefan Bröer, John E J Rasko, Juleen A Cavanaugh

Journal: Ann. Hum. Genet.. 2007 Nov;71(Pt 6):755-61.

 

Hartnup disorder is an aminoaciduria that results from mutations in the recently described gene SLC6A19 on chromosome 5p15.33. The disease is inherited in a simple recessive manner and ten different mutations have been described to date. One mutation, the D173N allele, is present ...

Last Updated: 4 Oct 2007

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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 "Hartnup Disease" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.