Organ involvement occurs in all forms of hereditary haemolytic anaemia

Br J Haematol. 2019 May;185(3):602-605. doi: 10.1111/bjh.15575. Epub 2018 Sep 5.

Authors

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.

PMID: 30183081
DOI: 10.1111/bjh.15575

No abstract available

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

Publication types

Clinical Trial
Letter
Observational Study

MeSH terms

Adolescent
Adult
Aged
Aged, 80 and over
Anemia, Hemolytic, Congenital / genetics
Anemia, Hemolytic, Congenital / metabolism*
Anemia, Hemolytic, Congenital / pathology*
Anemia, Hemolytic, Congenital / therapy
Cross-Sectional Studies
Female
Humans
Male
Middle Aged
Organ Specificity