Hereditary neutrophilia

Common Name(s)

Hereditary neutrophilia

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hereditary neutrophilia" 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 "Hereditary neutrophilia" returned 1 free, full-text research articles on human participants. First 3 results:

An activating mutation in the CSF3R gene induces a hereditary chronic neutrophilia.
 

Author(s): Isabelle Plo, Yanyan Zhang, Jean-Pierre Le Couédic, Mayuka Nakatake, Jean-Michel Boulet, Miki Itaya, Steven O Smith, Najet Debili, Stefan N Constantinescu, William Vainchenker, Fawzia Louache, Stéphane de Botton

Journal: J. Exp. Med.. 2009 Aug;206(8):1701-7.

 

We identify an autosomal mutation in the CSF3R gene in a family with a chronic neutrophilia. This T617N mutation energetically favors dimerization of the granulocyte colony-stimulating factor (G-CSF) receptor transmembrane domain, and thus, strongly promotes constitutive activation ...

Last Updated: 31 Dec 1969

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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 "Hereditary neutrophilia" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.