Literature DB >> 12571472

Paroxysmal nocturnal hemoglobinuria arising from Fanconi anemia.

Linda Wainwright1, Robert A Brodsky, Linda K Erasmus, Stelios Poyiadjis, Gita Naidu, Diane MacKinnon.   

Abstract

The progress of a female child with African type Fanconi anemia that evolves in time into paroxysmal nocturnal hemoglobinuria is described. Modern diagnostic methods are used to confirm this process. A discussion of possible mechanisms ensues.

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Year:  2003        PMID： 12571472     DOI： 10.1097/00043426-200302000-00017

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN： 1077-4114            Impact factor:   1.289


  3 in total

Review 1.  Paroxysmal nocturnal hemoglobinuria in children.

Authors:  Marry M van den Heuvel-Eibrink
Journal:  Paediatr Drugs       Date:  2007       Impact factor: 3.022

2.  The predictive value of PNH clones, 6p CN-LOH, and clonal TCR gene rearrangement for aplastic anemia diagnosis.

Authors:  Yash B Shah; Salvatore F Priore; Yimei Li; Chi N Tang; Peter Nicholas; Peter Kurre; Timothy S Olson; Daria V Babushok
Journal:  Blood Adv       Date:  2021-08-24

3.  Paroxysmal nocturnal hemoglobinuria in childhood and adolescence--a retrospective analysis of 18 cases.

Authors:  Rahul Naithani; Manoranjan Mahapatra; Pankhi Dutta; Rajat Kumar; Hara Prasad Pati; Ved Prakash Choudhry
Journal:  Indian J Pediatr       Date:  2008-08-31       Impact factor: 1.967
  3 in total

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