phenprocoumon and Zellweger-Syndrome

phenprocoumon has been researched along with Zellweger-Syndrome* in 1 studies

Other Studies

1 other study(ies) available for phenprocoumon and Zellweger-Syndrome

ArticleYear
[Symptomatic calcification in the newborn. Phenocopies of chondrodysplasia punctata].
    RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin, 1990, Volume: 152, Issue:4

    Stippled epiphyses occur in the new-born and young infant in the different hereditary forms of chondrodysplasia punctata. Symptomatic stippling has been described also in association with chromosomal anomalies, gangliosidosis and drug induced embryopathies. We present patients with Cumarin-embryopathy (2), fetal alcohol syndrome (1), Zellweger-syndrome (2) and chromosomal anomaly 16 (1) and discuss the typical roentgenographic features, distribution and differential diagnosis of epiphyseal stippling.

    Topics: 4-Hydroxycoumarins; Chondrodysplasia Punctata; Chromosome Aberrations; Chromosomes, Human, Pair 16; Female; Fetal Alcohol Spectrum Disorders; Humans; Infant, Newborn; Male; Maternal-Fetal Exchange; Phenprocoumon; Pregnancy; Zellweger Syndrome

1990