Abstract
A 35-month-old boy with non-mosaic Patau syndrome presented in diabetic ketoacidosis and was diagnosed with type 1 diabetes mellitus. A decision to treat this unanticipated medical problem was made in conjunction with the child’s parent, and he improved with fluid resuscitation and insulin treatment. Acute kidney injury with hypernatraemia complicated his treatment, but this resolved with careful intravenous fluid management. The child survived and was followed up in the diabetes clinic where ongoing management was complicated by persistent fetal haemoglobin, which meant that glycated haemoglobin could not be used to gauge his glucose control.
Reference8 articles.
1. Morris JK , Springett A . The National Down syndrome cytogenetic register for England and Wales: 2013 annual report. Queen Mary University of London, Barts and the London school of medicine and dentistry, 2014. Available: http://www.binocar.org/content/annrep2013_final_nologo.pdf
2. Survival of trisomy 18 (Edwards syndrome) and trisomy 13 (Patau syndrome) in England and Wales: 2004-2011;Wu;Am J Med Genet A,2013
3. Persistence of Hemoglobin F in D/D Translocation With Trisomy 13-15 (D1)
4. Persistence of fetal hemoglobin expression in an older child with trisomy 13;Sankaran;J Pediatr,2012
5. Population-Based Analyses of Mortality in Trisomy 13 and Trisomy 18
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