Porphyria, acute hepatic

Common Name(s)

Porphyria, acute hepatic

ALAD porphyria is a rare autosomal recessive disorder that has been reported and confirmed by genetic analysis in only 5 patients ({18:Jaffe and Stith, 2007}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Porphyria, acute hepatic" 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 "Porphyria, acute hepatic" returned 0 free, full-text research articles on human participants.

Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Porphyria, acute hepatic" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

EXPLORE: A Natural History Study of Acute Hepatic Porphyria (AHP)
 

Status: Recruiting

Condition Summary: Acute Hepatic Porphyria

 

Last Updated: 2 Jun 2017

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Dental Health, Diet, Inflammation and Biomarkers in Patients With Acute Intermittent Porphyria(AIP)
 

Status: Not yet recruiting

Condition Summary: Acute Intermittent Porphyria

 

Last Updated: 8 Jun 2012

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Controlled Trial of Panhematin in Treatment of Acute Attacks of Porphyria
 

Status: Recruiting

Condition Summary: Acute Porphyrias

 

Last Updated: 17 Aug 2017

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