Journal of Inherited Metabolic Disease · 1984 · 19 citations · 27 references
Life SciencesBiochemistryMolecular BiologyHuman GeneticsMolecular PathologyFatty Acid MetabolismGenetic DisordersLipid MetabolismLipid Metabolism DisordersMetabolic Pathway DefectsMetabolic SyndromeFatty Acid Oxidation Enzyme DeficienciesInherited Disorders Of Glycolipid MetabolismVery Long-chain Fatty Acid AccumulationZellweger Spectrum DisordersZellweger Syndrome
The very long chain fatty acids in cultured fibroblasts from six patients with the cerebro-hepato-renal syndrome of Zellweger, from six of their parents, from three controls, and also in three amniotic fluid control cell lines were analysed by gas chromatography. Increased concentrations of hexacosanoic acid (C26:O) were consistently found in the Zellweger syndrome. Also the ratios C26:O/C22:O, C25:O/C22:O, and C24:O/C22:O were elevated. The very long chain fatty acid levels and ratios in fibroblasts from the patients' parents were within the normal range. Findings in amniotic fluid cell lines indicate the possibility of antenatal diagnosis for Zellweger's syndrome. The similarities between neonatal adrenoleukodystrophy and Zellweger's syndrome suggest the applicability of this technique also in neonatal adrenoleukodystrophy.
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Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome
Sidney Goldfischer, Cyril L. Moore, Alfred J. Spiro et al. · Science · 1973 · 794 citations
Herbert H. Schaumburg · Archives of Neurology · 1975 · 474 citations
Hugo W. Moser, Ann B. Moser, Karen K. Frayer et al. · Neurology · 1981 · 397 citations · Full text
Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome)
H. S. A. Heymans, R. B. H. Schutgens, Raymond K. Tan et al. · Nature · 1983 · 351 citations
Medicine, Pathology, Pediatrics +13
Barbara R. Migeon, H. W. Moser, Ann B. Moser et al. · Proceedings of the National Academy of Sciences · 1981 · 291 citations · Full text