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Short Report

Broadening the spectrum of neonatal hemochromatosis

ORCID Icon, , , , &
Pages 1024-1026 | Received 03 Feb 2018, Accepted 26 Jul 2018, Published online: 10 Sep 2018

References

  • Pan X, Kelly S, Melin-Aldana H, et al. Novel mechanism of fetal hepatocyte injury in congenital alloimmune hepatitis involves the terminal complement cascade. Hepatology. 2010;51:2061–2068.
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  • Kelly AL, Lunt PW, Rodrigues F, et al. Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolism. J Med Genet. 2001;38:599–610.
  • Whitington PF, Hibbard JU. High-dose immunoglobulin during pregnancy for recurrent neonatal haemochromatosis. Lancet 2004;364:1690–1698.
  • Ekong UD, Kelly S, Whitington PF. Disparate clinical presentation of neonatal hemochromatosis in twins. Pediatrics 2005;116:e880–e884.
  • Collardeau-Frachon S, Heissat S, Bouvier R, et al. French retrospective multicentric study of neonatal hemochromatosis: importance of autopsy and autoimmune maternal manifestations. Pediatr Dev Pathol. 2012;15:450–470.
  • Mackay RJ, Bratkovic D, Couper R, et al. Detection of treatable neonatal liver disease by expanded newborn screening. J Inherit Metab Dis. 2008;31:271–S273.

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