
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.
Male, Orotic Acid, Genetic Linkage, Genetic Carrier Screening, Chromosome Mapping, Genetic Counseling, Ornithine Carbamoyltransferase Deficiency Disease, Pedigree, Ammonia, Risk Factors, Humans, Female, Amino Acid Metabolism, Inborn Errors, Ornithine Carbamoyltransferase, Polymorphism, Restriction Fragment Length
Male, Orotic Acid, Genetic Linkage, Genetic Carrier Screening, Chromosome Mapping, Genetic Counseling, Ornithine Carbamoyltransferase Deficiency Disease, Pedigree, Ammonia, Risk Factors, Humans, Female, Amino Acid Metabolism, Inborn Errors, Ornithine Carbamoyltransferase, Polymorphism, Restriction Fragment Length
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