Genetic counseling in ornithine carbamoyltransferase deficiency |
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Authors: | A Pelet E Toumas D Rabier J Kaplan P Kamoun J Frezal J M Saudubray A Munnich |
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Affiliation: | Clinique et Unité de Recherches de Génétique Médicale, INSERM U 12, H?pital des Enfants Malades, Paris. |
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Abstract: | Ornithine transcarbamylase (OTC) deficiency is an inborn error of urea cycle metabolism, responsible for lethal hyperammonemia in males and for severe symptoms in at least 20% of heterozygous females. The authors provide here additional data on the informativity of the protein loading test (PLT) for the detection of heterozygotes. They show that the risk of being a carrier for the mother of an affected boy falls from 2/3 a priori to only 1/8 if her PLT is negative. The risk for the mother of heterozygote girl falls from 1/2 a priori to 1/16 if her PLT is negative. |
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