Respiratory Distress in a Late Preterm: Is it Sepsis or Inborn Error of Metabolism?
Author:
Affiliation:
1. *Neonatal Intensive Care Unit, Pakistan Emirates Military Hospital, Rawalpindi, Pakistan
Publisher
American Academy of Pediatrics (AAP)
Link
https://publications.aap.org/neoreviews/article-pdf/25/6/e366/1652465/neoreviews.052023iositn00096.pdf
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3. Application of multiplex ligation-dependent probe amplification, and identification of a heterozygous Alu-associated deletion and a uniparental disomy of chromosome 1 in two patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency;Aoyama;Int J Mol Med,2015
4. 3-Hydroxy-3-methylglutaric aciduria with bilateral basal ganglia lesion: a case report;Hao;Exp Ther Med,2016
5. A case of dilated cardiomyopathy associated with 3-hydroxy-3-methylglutaryl-coenzyme A (HMG CoA) lyase deficiency;Leung;Case Rep Med,2009
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