Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome

J. M. Powers, R. C. Tummons, A. B. Moser, H. W. Moser, D. S. Huff, R. I. Kelley

Research output: Contribution to journalArticlepeer-review

16 Scopus citations


Neuropathological examination of three males with cerebro-hepato-renal (Zellweger) syndrome (CHRS) revealed selective neuronal lipidosis and neuroaxonal dystrophy of the dorsal nucleus of Clarke and lateral cuneate nucleus. This lipidotic alteration was visualized as perikaryal or axonal enlargements with cytoplasmic striations. With the light microscope, the striated material was birefringent and resistant to traditional lipid stains; ultrastructurally, it was composed of lipid clefts, lamellae and lamellar-lipid profiles; biochemically, the affected region contained large amounts of cholesterol esterified to very long-chain fatty acids, both saturated and mounounsaturated. This metabolic lesion, though localized to specific sensory neurons, suggests that a more generalized defect in neuronal fatty acid metabolism may be operative in CHRS.

Original languageEnglish (US)
Pages (from-to)333-343
Number of pages11
JournalActa neuropathologica
Issue number4
StatePublished - Dec 1 1987


  • Adreno-leukodystrophy
  • Cytoplasmic striations
  • Fatty acids
  • Neuronal migrations
  • Zellweger

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Clinical Neurology
  • Cellular and Molecular Neuroscience


Dive into the research topics of 'Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome'. Together they form a unique fingerprint.

Cite this