Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: a case report

Author:

Shin Chungwoo,Hong Mee,Kim Myungshin,Lee Jung HyunORCID

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Viana MB, Belisário AR. De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth. Rev Bras Hematol Hemoter. 2014;36:230–4.

2. Estey MP, Clarke G, Sia W, Toor E, Higgins TN. A mother and newborn with brown blood. Clin Chem. 2015;61:466–9.

3. Haymond S. Oxygen saturation: a guide to laboratory assessment. Clin Lab News. 2006:10–2.

4. Nagel RL. Disorders of hemoglobin function and stability. In: Steinberg MH, forget BG, Higgs DR, et al. disorders of hemoglobin: genetics, pathophysiology and clinical management. Cambridge: Cambridge University Press; 2001. p. 1155–94.

5. Elboraee MS, Clarke G, Belletrutti MJ, Escoredo S. HbM methaemoglobinaemia as a rare case of early neonatal benign cyanosis. BMJ Case Rep. 2015; pii:bcr2015212336.

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