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SQUMJ-Sultan Qaboos University Medical Journal. 2012; 12 (4): 498-502
in English | IMEMR | ID: emr-126011

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


Subject(s)
Humans , Male , Myeloproliferative Disorders/diagnosis , Leukemia, Myeloid, Acute , Karyotyping , Infant, Premature , Myeloproliferative Disorders/complications
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