Pyropoikilocytosis hereditary

Common Name(s)

Pyropoikilocytosis hereditary

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

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

Nonsense mutations of the alpha-spectrin gene in hereditary pyropoikilocytosis.
 

Author(s): Whitney Tolpinrud, Yelena D Maksimova, Bernard G Forget, Patrick G Gallagher

Journal: Haematologica. 2008 Nov;93(11):1752-4.

 

Last Updated: 3 Nov 2008

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Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.
 

Author(s): May-Jean King, Paul Telfer, Heather MacKinnon, Lisa Langabeer, Corrina McMahon, Philip Darbyshire, Didier Dhermy

Journal: Cytometry B Clin Cytom. 2008 Jul;74(4):244-50.

 

Flow cytometric analysis of eosin-5-maleimide (EMA)-labeled red blood cells (RBCs) has been used as a screening test for the diagnosis of patients with hereditary spherocytosis (HS). We assessed the fluorescence profiles for patients having HS and hereditary pyropoikilocytosis (HPP) ...

Last Updated: 18 Jun 2008

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A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred.
 

Author(s): Daniel B Costa, Larisa Lozovatsky, Patrick G Gallagher, Bernard G Forget

Journal: Blood. 2005 Dec;106(13):4367-9.

 

Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia due to abnormalities of the red blood cell (RBC) membrane skeleton. In the original HPP kindred, there is compound heterozygosity for an allele encoding a structural variant of alpha-spectrin (L207P) and an alpha-spectrin ...

Last Updated: 5 Dec 2005

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Reviews from the PubMed Database

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The terms "Pyropoikilocytosis hereditary" 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

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