Abstract
A newborn infant who presented with central cyanosis was found to have hereditary methaemoglobinaemia. The pulse oximeter readings and physical findings were incompatible. Clinical assessment remains an important part in the management of such cases.
| Original language | English |
|---|---|
| Pages (from-to) | 94-95 |
| Journal | Journal of paediatrics and child health |
| Volume | 37 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2001 |
| Externally published | Yes |
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