Neonatal adrenoleukodystrophy

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

Genetic disorder, organelle: Peroxisomal disorders and lysosomal structural disorders (E80.3, 277.86)

Peroxisome biogenesis disorder	Zellweger syndrome Neonatal adrenoleukodystrophy Infantile Refsum disease Adult Refsum disease-2 RCP 1

Enzyme-related	Acatalasia RCP 2&3 Mevalonate kinase deficiency D-bifunctional protein deficiency Adult Refsum disease-1

Transporter-related	X-linked adrenoleukodystrophy

Lysosomal	Danon disease

See also: proteins, intermediates

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