Hyperinsulinism-hyperammonemia syndrome

Common Name(s)

Hyperinsulinism-hyperammonemia syndrome

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hyperinsulinism-hyperammonemia syndrome" 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 "Hyperinsulinism-hyperammonemia syndrome" returned 4 free, full-text research articles on human participants. First 3 results:

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients.
 

Author(s): Adrijan Sarajlija, Tatjana Milenkovic, Maja Djordjevic, Katarina Mitrovic, Sladjana Todorovic, Bozica Kecman, Khalid Hussain

Journal: J Clin Res Pediatr Endocrinol. 2016 Jun;8(2):228-31.

 

Hyperinsulinism/hyperammonemia (HI/HA) syndrome is considered as the second most common type of hereditary HI. Correlation of genotype and phenotype in HI/HA syndrome has been described in several studies. We present three Serbian patients with HI/HA syndrome with emphasis on a possible ...

Last Updated: 9 Jun 2016

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Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene.
 

Author(s): Maria Lúcia Corrêa-Giannella, Daniel Soares Freire, Ana Mercedes Cavaleiro, Maria Angela Zanella Fortes, Ricardo Rodrigues Giorgi, Maria Adelaide Albergaria Pereira

Journal: Arq Bras Endocrinol Metabol. 2012 Nov;56(8):485-9.

 

The hyperinsulinism/hyperammonemia (HI/HA) syndrome is a rare autosomal dominant disease manifested by hypoglycemic symptoms triggered by fasting or high-protein meals, and by elevated serum ammonia. HI/HA is the second most common cause of hyperinsulinemic hypoglycemia of infancy, ...

Last Updated: 8 Jan 2013

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[Hyperinsulinism-hyperammonemia syndrome due to a de novo mutation in exon 7 (G979A) of the glutamate dehydrogenase gene with excellent response to diazoxide].
 

Author(s): C Montero Luis, J Pozo Román, María T Muñoz Calvo, G Martos Moreno, María A Donoso, O Rubio Cabezas, J Argente Oliver

Journal: An Pediatr (Barc). 2004 Nov;61(5):433-7.

 

Hyperinsulinism-hyperammonemia syndrome is characterized by recurrent and symptomatic hypoglycemias in childhood, secondary to hyperinsulinism associated with mild and asymptomatic hyperammonemia. This syndrome is caused by dominantly expressed mutations of the glutamate dehydrogenase ...

Last Updated: 8 Nov 2004

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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 "Hyperinsulinism-hyperammonemia syndrome" 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.