Organ involvement occurs in all forms of hereditary haemolytic anaemia

Stephanie van Straaten^{1

2}, Jill Verhoeven^{1

2}, Sanne Hagens^{1

2}, Roger Schutgens², Wouter van Solinge¹, Richard van Wijk¹, Eduard J van Beers²

Affiliations

¹ Laboratory of Clinical Chemistry & Haematology, University Medical Centre Utrecht, Utrecht, Netherlands.
² Van Creveldkliniek, University Medical Centre Utrecht, Utrecht, Netherlands.

Observational Study

Stephanie van Straaten et al. Br J Haematol. 2019 May.

. 2019 May;185(3):602-605.

doi: 10.1111/bjh.15575. Epub 2018 Sep 5.

Stephanie van Straaten^{1

2}, Jill Verhoeven^{1

2}, Sanne Hagens^{1

2}, Roger Schutgens², Wouter van Solinge¹, Richard van Wijk¹, Eduard J van Beers²

¹ Laboratory of Clinical Chemistry & Haematology, University Medical Centre Utrecht, Utrecht, Netherlands.
² Van Creveldkliniek, University Medical Centre Utrecht, Utrecht, Netherlands.

No abstract available

Keywords: haemolytic anaemia; pyruvate kinase deficiency; sickle cell disease; spherocytosis; β-thalassaemia.

Publication types