Abstract
Membrane disorders comprise an important group of inherited haemolytic anaemias. Diagnostic work-up starts with examination of the blood smear, followed by osmotic gradient ektacytometry. In special cases DNA analysis is performed to confirm the diagnosis. For this purpose a next-generation sequencing-based method has been developed. The combination of these techniques established the correct diagnosis in a case of haemolytic anaemia of unknown cause.
| Original language | English |
|---|---|
| Pages (from-to) | 86-89 |
| Number of pages | 4 |
| Journal | Netherlands Journal of Medicine |
| Volume | 73 |
| Issue number | 2 |
| Publication status | Published - 2015 |
Keywords
- Blood smear
- Hemolytic anemia
- Next generation sequencing