Prenatal diagnosis of ornithine transcarbamylase deficiency utilizing fetal liver biopsy.

W Holzgreve, MS Golbus - American journal of human genetics, 1984 - ncbi.nlm.nih.gov
W Holzgreve, MS Golbus
American journal of human genetics, 1984ncbi.nlm.nih.gov
The prenatal diagnosis of ornithine transcarbamylase deficiency (OTCD) was made by using
radioactive microassays for ornithine transcarbamylase (OTC) and--as an internal control--
carbamyl phosphate synthetase (CPS I) in liver biopsy material from two 19-week-old at-risk
fetuses. In each case, no OTC activity could be detected, while CPS I activity was normal.
Control fetuses of 17-21 weeks gestation had OTC activities in the range of 10.7 to 19.4
mumol/mg protein per hr. The prenatal results were confirmed post abortum by the …
Abstract
The prenatal diagnosis of ornithine transcarbamylase deficiency (OTCD) was made by using radioactive microassays for ornithine transcarbamylase (OTC) and--as an internal control--carbamyl phosphate synthetase (CPS I) in liver biopsy material from two 19-week-old at-risk fetuses. In each case, no OTC activity could be detected, while CPS I activity was normal. Control fetuses of 17-21 weeks gestation had OTC activities in the range of 10.7 to 19.4 mumol/mg protein per hr. The prenatal results were confirmed post abortum by the radiochemical assays and by an enzyme-specific cytochemical staining method.
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