| Literature DB >> 27718309 |
Leo Kager1,2, Lesley J Bruce3, Petra Zeitlhofer4, Joanna F Flatt3, Tabita M Maia5, M Leticia Ribeiro5, Bernhard Fahrner1, Gerhard Fritsch2, Kaan Boztug1,6, Oskar A Haas1,2.
Abstract
We describe the second patient with anionic exchanger 1/band 3 null phenotype (band 3 nullVIENNA ), which was caused by a novel nonsense mutation c.1430C>A (p.Ser477X) in exon 12 of SLC4A1. We also update on the previous band 3 nullCOIMBRA patient, thereby elucidating the physiological implications of total loss of AE1/band 3. Besides transfusion-dependent severe hemolytic anemia and complete distal renal tubular acidosis, dyserythropoiesis was identified in the band 3 nullVIENNA patient, suggesting a role for band 3 in erythropoiesis. Moreover, we also, for the first time, report that long-term survival is possible in band 3 null patients.Entities:
Keywords: hematology; hemolytic anemias; molecular genetics; nonmalignant; red blood cell disorders
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Year: 2016 PMID: 27718309 DOI: 10.1002/pbc.26227
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167