[ English | Bahasa Malaysia ] Hari ini ialah 1 Dec 2023, 02:10 AM (Terakhir dikemaskini pada: 27th Nov 2023)

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Anasufiza Habib, Zabedah Md Yunus, Nor Azimah Azize, Gaik-Siew Ch'ng, Winnie Pei Tee Ong, Bee-Chin Chen, Ho-Torng Hsu, Ke-Juin Wong, James Pitt and Lock-Hock Ngu (2013). Hyperexcretion of homocitrulline in a Malaysian patient with lysinuric protein intolerance. European Journal of Pediatric 172(9): 1277-1281

Abstract :

Lysinuric protein intolerance (LPI; MIM 222700) is an inherited aminoaciduria with an autosomal recessive mode of inheritance. Biochemically, affected patients present with increased excretion of the cationic amino acids: lysine, arginine, and ornithine. We report the first case of LPI diagnosed in Malaysia presented with excessive excretion of homocitrulline. The patient was a 4-year-old male who presented with delayed milestones, recurrent diarrhea, and severe failure to thrive. He developed hyperammonemic coma following a forced protein-rich diet. Plasma amino acid analysis showed increased glutamine, alanine, and citrulline but decreased lysine, arginine and ornithine. Urine amino acids showed a marked excretion of lysine and ornithine together with a large peak of unknown metabolite which was subsequently identified as homocitrulline by tandem mass spectrometry. Molecular analysis confirmed a previously unreported homozygous mutation at exon 1 (235 G > A, p.Gly79Arg) in the SLC7A7 gene. This report demonstrates a novel mutation in the SLC7A7 gene in this rare inborn error of diamino acid metabolism. It also highlights the importance of early and efficient treatment of infections and dehydration in these patients. Conclusion: The diagnosis of LPI is usually not suspected by clinical findings alone, and specific laboratory investigations and molecular analysis are important to get a definitive diagnosis.




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