First prenatal diagnosis of acyl-CoA oxidase deficiency

Author:

Wanders R. J. A.,Schelen A.,Feller N.,Schutgens R. B. H.,Stellaard F.,Jakobs C.,Mitulla B.,Seidlitz G.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference7 articles.

1. Jakobs, C., ten Brink, H., Kok, R. M., Stellaard, F., Kleijer, W. J., Wanders, R. J. A. and Schutgens, R. B. H. Very long chain fatty acids in amniotic fluid from a fetus affected with Zellweger syndrome.Eur. J. Pediatr. 148 (1989) 581

2. Kelley, R. I., Datta, N. S., Dobijns, W. S., Hajra, A. K., Moser, A. B., Noetzel, M.J., Zackai, E. H. and Moser, H. W. Neonatal adrenoleukodystrophy: new cases, biochemical studies and differentiation from Zellweger, and related polydystrophy syndromes.Am. J. Med. Genet. 23 (1986) 869–901

3. Lazarow, P. B. and de Duve, C. A fatty acyl-CoA oxidizing system in rat liver peroxisomes: enhancement by clofibrate, a hypolipidemic drug.Proc. Natl. Acad. Sci. USA 73 (1976) 2043–2046

4. Poll-The, B. T., Roels, F., Ogier, H., Scotto, J., Vamecq, J., Schutgens, R. B. H., Wanders, R. J. A., van Roermund, C. W. T., van Wijland, M. J. A., Schram, A. W., Tager, J. M. and Saudubray, J. M. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).Am. J. Hum. Genet. 42 (1988) 422–434

5. Schutgens, R. B. H., Schrakamp, G., Wanders, R. J. A., Heymans, H. S. A., Tager, J. M. and van den Bosch, H. Prenatal and perinatal diagnosis of peroxisomal disorders.J. Inher. Metab. Dis. 12 Suppl. 1 (1989) 118–134

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