Home > Journals > Biology and research > Annales de Biologie Clinique > summary
 
      Advanced search    Shopping cart    French version 
 
Latest books
Catalogue/Search
Collections
All journals
Medicine
Biology and research
Annales de Biologie Clinique
- Current issue
- Archives
- Subscribe
- Order an issue
- More information
Public health
Agronomy and biotech.
My account
Forgotten password?
Online account   activation
Subscribe
Licences IP
- Instructions for use
- Estimate request form
- Licence agreement
Order an issue
Pay-per-view articles
Newsletters
How can I publish?
Journals
Books
Help for advertisers
Foreign rights
Book sales agents



 

Texte intégral de l'article
 
Printable version

Extra medullary hematopoiesis associated to congenital dyserythropoietic anemia II in adult


Annales de Biologie Clinique. Volume 70, Number 2, 217-20, Mars-Avril 2012, Biologie au quotidien

Résumé   Texte intégral  

Author(s) : Inès Jedidi, Moez Medhaffar, Manel Ghorbel, Sondes Hdiji, Faiza Makni, Moez Elloumi, Choumous Kallel

Summary : The congenital dyserythropoietic anemias comprise a group of rare hereditary disorders of erythropoiesis characterized by anemia with ineffective erythropoiesis and morphological abnormalities of erythroblasts in the bone marrow. Congenital dyserythropoietic anemia type II or HEMPAS is the more frequent type. It is rare in adults. Extra medullary hematopoiesis is also a rare entity\; it is a physiological response to chronic anemia observed in certain hemopathies like congenital dyserythropoietic anemia type II. We report the observation of a patient for who diagnosis of extra medullary hematopoiesis associated to congenital dyserythropoietic type II was made in adulthood.

Keywords : congenital dyserythropoietic anemia type II (CDA II), HEMPAS, extra medullary hematopoiesis

 

About us - Contact us - Conditions of use - Secure payment
Latest news - Conferences
Copyright © 2007 John Libbey Eurotext - All rights reserved
[ Legal information - Powered by Dolomède ]