Neonatal_adrenoleukodystrophy

Neonatal adrenoleukodystrophy

Neonatal adrenoleukodystrophy

Medical condition

For the X-linked, juvenile or adult-onset condition, see 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]

Quick Facts Other names ...

References

  1. [1]
    RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Neonatal adrenoleukodystrophy". www.orpha.net. Retrieved 17 March 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
  2. [2]
    "#202370 Adrenoleukodystrophy, Autosomal Neonatal Form". Johns Hopkins University. Retrieved 2012-06-24.
Stub icon

This genetic disorder article is a stub. You can help Wikipedia by expanding it.
Share this article:

This article uses material from the Wikipedia article Neonatal_adrenoleukodystrophy, and is written by contributors. Text is available under a CC BY-SA 4.0 International License; additional terms may apply. Images, videos and audio are available under their respective licenses.