| Literature DB >> 15635485 |
Kouhei Ishiwari1, Masaharu Kotani2, Minoru Suzuki3, Elena Pumbo3, Akemi Suzuki3, Toshihide Kobayashi3, Tamaki Ueno1, Tomoko Fukushige4, Tamotsu Kanzaki4, Masato Imada5, Kohji Itoh6, Shinji Akioka7, Youichi Tajima2, Hitoshi Sakuraba8.
Abstract
We report the first Japanese case of Salla disease. A 5-year-old male patient developed unique proteinuria with other clinical manifestations, including coarse facies, dysostosis multiplex, mild mitral valve regurgitation, umbilical and inguinal herniation, and mild developmental delay. Pathological analysis of biopsied kidney tissues showed marked vacuolation of podocytes, mesangial cells, capillary endothelial cells, and tubular cells. Biochemical studies involving thin-layer chromatography and mass spectrometry revealed increased excretion of free sialic acid (N-acetylneuraminic acid) into the patient's urine. Immuno- and lectin staining of the patient's cells demonstrated the accumulation of sialyl and asialyl glycoconjugates in lysosomes and late endosomes. A defect in sialyl glycoconjugate metabolism is thought to have occurred in the patient's cells, besides impairment of the lysosomal transport of free sialic acid residues. A renal disorder should be considered as an important manifestation, not only in infantile free sialic acid storage disease but also in Salla disease.Entities:
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Year: 2004 PMID: 15635485 DOI: 10.1007/s10038-004-0203-y
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172