Zellweger syndrome: Depiction of MRI findings in early infancy at 3.0 Tesla

Cory M. Pfeifer, Carlos A. Martinot

Research output: Contribution to journalArticlepeer-review

7 Scopus citations


Zellweger syndrome, also referred to as cerebrohepatorenal syndrome, is a rare autosomal recessive disease representing the most severe form of the peroxisomal biogenesis disorders. Neuroanatomical sequelae include impaired neuronal migration, diffuse hypomyelination, and sensorineural degeneration. Due to the rare and severe nature of this disorder, early mortality, and comorbidities that place the patient at risk for sedated imaging, high-resolution magnetic resonance imaging findings of Zellweger syndrome are scarce in the literature. Presented here is a case of this rare disease imaged at 3.0 Tesla.

Original languageEnglish (US)
Pages (from-to)442-444
Number of pages3
JournalNeuroradiology Journal
Issue number5
StatePublished - Oct 1 2017


  • Cerebrohepatorenal syndrome
  • Zellweger syndrome
  • peroxisomal disorder

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging
  • Clinical Neurology


Dive into the research topics of 'Zellweger syndrome: Depiction of MRI findings in early infancy at 3.0 Tesla'. Together they form a unique fingerprint.

Cite this