Abstract
Serum thymidine kinase (TK) was determined in a family with congenital dyserythropoietic anaemia type m (CDA, type III). 20 patients and 10 of their healthy siblings were investigated. Elevated TK was found in all 20 patients (median 56.2 U) but their healthy siblings had normal values (median 2.65 U). We suggest that determination of TK should be used for discrimination between healthy siblings and individuals affected by CDA type III when bone marrow examination is not suitable.
Original language | English |
---|---|
Pages (from-to) | 653-654 |
Journal | British Journal of Haematology |
Volume | 87 |
Issue number | 3 |
DOIs | |
Publication status | Published - 1994 |
Externally published | Yes |
Subject classification (UKÄ)
- Hematology
Free keywords
- Autosomal dominant
- CDA type III
- Haemolytic anaemia
- Thymidine kinase