| Literature DB >> 25277063 |
Roberto H Nussenzveig1, Robert D Christensen, Josef T Prchal, Hassan M Yaish, Archana M Agarwal.
Abstract
We evaluated a neonate with severe jaundice but a negative family history. Spherocytes were present and suspected hereditary spherocytosis was confirmed by osmotic fragility and eosin-5-maleimide erythrocyte staining. We found he was a compound heterozygote for two pathogenic mutations in the gene encoding α-spectrin: a previously reported α(LEPRA) inherited from his asymptomatic mother, and a novel α-spectrin mutation in intron 45 +1 disrupting the consensus splice site, from his asymptomatic father.Entities:
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Year: 2014 PMID: 25277063 DOI: 10.1159/000365586
Source DB: PubMed Journal: Neonatology ISSN: 1661-7800 Impact factor: 4.035