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Up to: Urea cycle disorder or inherited hyperammonemia · Citrullinemia
Citrullinemia type I
Citrullinemia type I is a rare autosomal recessive urea cycle defect characterized biologically by hyperammonemia and clinically by progressive lethargy, poor feeding and vomiting in the neonatal form (Acute neonatal citrullinemia type I) and by variable hyperammonemia in the later-onset form (adult-onset citrullinemia type I).
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Acute neonatal citrullinemia type I 0 trials
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Adult-onset citrullinemia type I 0 trials