Neonatal adrenoleukodystrophy

Neonatal adrenoleukodystrophy is an inborn error of peroxisome biogenesis. It is part of the Zellweger spectrum. It has been linked with multiple genes (at least five) associated with peroxisome biogenesis, and has an autosomal recessive pattern of inheritance.[2]

For the X-linked, juvenile or adult-onset condition, see Adrenoleukodystrophy.
Neonatal adrenoleukodystrophy
Other namesNALD[1]

References
  1. RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Neonatal adrenoleukodystrophy". www.orpha.net. Retrieved 17 March 2019.
  2. "#202370 Adrenoleukodystrophy, Autosomal Neonatal Form". Johns Hopkins University. Retrieved 2012-06-24.
Classification
External resources
  • Orphanet: 44
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