Prenatal diagnosis of rhizomelic chondrodysplasia punctata |
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Authors: | S Hoefler G Hoefler A B Moser P A Watkins W W Chen H W Moser |
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Institution: | The Kennedy Institute for Handicapped Children and Department of Neurology and Pediatrics, John Hopkins University. U.S.A. |
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Abstract: | Plasmalogen biosynthesis and phytanic acid oxidation activity were measured in cultured chorionic villus samples or amniocytes from four pregnancies at risk for the rhizomelic form of chondrodysplasia punctata (RCDP). Normal results were obtained in three of the samples and post-natal examination or fetal ultrasound studies confirmed that the fetuses were unaffected. Chorionic villus culture in one case demonstrated defective plasmalogen biosynthesis and lack of phytanic acid oxidation. Pregnancy was interrupted at 10 weeks. Immunoblot studies of post-mortem fetal tissues showed thatperoxisomal 3-oxoacyl-coenzyme A thiolase was present in the unprocessed form, a finding we had previously demonstrated in RCDP. These results establish that RCDP can be identified prenatally. |
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Keywords: | Rhizomelic chondrodysplasia punctata Chorionic villus cells Plasmalogen biosynthesis Phytanic acid oxidation 3-Oxoacyl-coenzyme A thiolase |
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