Abstract
An extremely premature male neonate presented with an unusual multisystem dysfunction within the first 24 to 48 hours of life. The unfolding of clinical events and investigations revealed a transient myeloproliferative disorder (TMD). TMD was the main indication for karyotyping of this premature infant without clinical symptoms of Down syndrome. The awareness of TMD in a newborn warrants karyotype analysis to look for trisomy 21 and a close surveillance because of its potential progression to true leukaemia.
Original language | English |
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Pages (from-to) | 498-502 |
Number of pages | 5 |
Journal | Sultan Qaboos University Medical Journal |
Volume | 12 |
Issue number | 4 |
DOIs | |
Publication status | Published - Nov 2012 |
Keywords
- Acute myelogenous leukemia (AML)
- Case report
- Down syndrome
- Extreme premature
- GATA1
- Oman
- Transient myeloproliferative disorder
ASJC Scopus subject areas
- Medicine(all)