An elderly Japanese patient with adult-onset type II
citrullinemia with a novel D493G mutation in the SLC25A13 gene.
She was admitted to Salmaniya Medical Complex (SMC) on May 1 to receive treatment for
citrullinemia, a disorder that causes ammonia and other toxic substances to accumulate in the blood.
Samples with a secondary cause of underglycosylation were from 1 patient with severe liver failure of unknown etiology, 1 patient with
citrullinemia type I with liver failure, 1 patient with hemophagocytic lymphohistiocytosis, and 1 patient with HUS due to Streptococcus pneumoniae infection who was positive for plasma sialidase (specific activity, 41 100 pmol x [h.sup.-1] x [mL.sup.-1] at pH 7.0; undetectable in controls).
Two-year-old Emaan Salman was admitted to Salmaniya Medical Complex (SMC) on May 1 to receive treatment for
Citrullinemia, a disorder that causes ammonia and other toxic substances to accumulate in the blood.
These values may be observed in infants with classic
citrullinemia, which would most likely be detectable after prolonged storage without correction for storage time.
In January 2002, six more tests were added for the fatty acid oxidation disorders (MCAD, SCAD, LCAD and VLCAD) and two urea cycle disorders, arginosuccinic acidemia and
citrullinemia.
We analyzed two urine samples from a patient with
citrullinemia. The urine [sup.1]H-NMR spectrum showed citrulline multiplets (concentration, 825 [micro]mol/mmol of creatinine).
In acute neonatal
citrullinemia, citrulline is substantially increased.
Des Moines, IA 50315 (515) 287-6798 (voice/fax) ??Jackie/Barker@hotmail.com 3,9 CHROMOSOME TRANSLOCATIONS See: Chromosome Deletions CHROMOSOME TRISOMY DISORDERS See: Chromosome 13 & 18 Disorders CHRONIC ENCEPHALITIS & EPILEPSY See: Rasmussen Syndrome CHRONIC FATIGUE SYNDROME CFIDS Association of America PO Box 220398 Charlotte, NC 28222-0398 (800) 442-3437 (704) 365-9755 (fax) ??info@cfids.org http://www.cfids.org 1,2,4,6,8 CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY See: Autoimmune Disorders CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY See: Guillain-Barre Syndrome CHRONIC LOCALIZED ENCEPHALITIS See: Rasmussen Syndrome
CITRULLINEMIA See: Urea Cycle Disorders CLEFT PALATE See also: Craniofacial Disorders Cleft Palate Foundation 104 Estes Dr., Ste.
Thus, ORA aciduria is observed in patients with ornithine carbamoylasetransferase deficiency (OCTD), an X-linked disorder, and could reveal heterozygosity after a protein load, and in
citrullinemia, argininosuccinic aciduria, and argininemia (2, 3).
Adult-onset type II
citrullinemia is associated with increased expression of TATI/PSTI in the liver and clearly increased serum concentrations.