Neonatal adrenoleukodystrophy

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For the X-linked, juvenile or adult-onset condition, see Adrenoleukodystrophy.
Neonatal adrenoleukodystrophy
Classification and external resources
OMIM 202370

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.[1]

References[edit]

  1. ^ "#202370 Adrenoleukodystrophy, Autosomal Neonatal Form". Johns Hopkins University. Retrieved 2012-06-24.