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Concept information

Preferred term

Zellweger Syndrome  

Type

  • Topical Descriptor

Entry terms

  • Cerebro Hepato Renal Syndrome
  • Cerebro-Hepato-Renal Syndrome
  • Cerebrohepatorenal Syndrome
  • Zellweger Disease
  • Zellweger's Syndrome

Scope note

  • An autosomal recessive disorder due to defects in PEROXISOME biogenesis which involves more than 13 genes encoding peroxin proteins of the peroxisomal membrane and matrix. Zellweger syndrome is typically seen in the neonatal period with features such as dysmorphic skull; MUSCLE HYPOTONIA; SENSORINEURAL HEARING LOSS; visual compromise; SEIZURES; progressive degeneration of the KIDNEYS and the LIVER. Zellweger-like syndrome refers to phenotypes resembling the neonatal Zellweger syndrome but seen in children or adults with apparently intact peroxisome biogenesis.

History note

  • 1989

In other languages

URI

http://www.yso.fi/onto/mesh/D015211

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