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Genetic counseling in ornithine carbamoyltransferase deficiency
Authors:A Pelet  E Toumas  D Rabier  J Kaplan  P Kamoun  J Frezal  J M Saudubray  A Munnich
Institution:Clinique et Unité de Recherches de Génétique Médicale, INSERM U 12, H?pital des Enfants Malades, Paris.
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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