The Pyruvate Kinase Deficiency Global Longitudinal (Peak) Registry: rationale and study design

Introduction Pyruvate kinase (PK) deficiency is a rare, under-recognised, hereditary condition that leads to chronic haemolytic anaemia and potentially serious secondary complications, such as iron overload, cholecystitis, pulmonary hypertension and extramedullary haematopoiesis. It is an autosomal...

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Bibliographic Details

Published in:	BMJ Open
Main Authors:	Yan Yan, Junlong Li, D Mark Layton, Rachael F Grace, Vip Viprakasit, Eduard J van Beers, Joan-Lluis Vives Corrons, Bertil Glader, Andreas Glenthøj, Hitoshi Kanno, Kevin H M Kuo, Carl Lander, Dagmar Pospíŝilová, Audra N Boscoe, Chris Bowden, Paola Bianchi
Format:	Article
Language:	English
Published:	BMJ Publishing Group 2023-03-01
Online Access:	https://bmjopen.bmj.com/content/13/3/e063605.full