Literature DB >> 30056406

[Transaldolase deficiency - clinical outcome, pathogenesis, diagnostic process].

Patryk Lipiński1, Teresa Stradomska2, Anna Tylki-Szymańska3.   

Abstract

Transaldolase deficiency is a rare inborn autosomal recessive error of the pentose phosphate pathway that, to date, has been diagnosed in 33 patients, including 4 from Poland. The aim of this manuscript was to present the clinical presentation, pathogenesis and diagnostic process of transaldolase deficiency. The authors also present a diagnostic algorithm of transaldolase deficiency.

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Keywords:  pentose phosphate pathway; polyols; transadolase deficiency; transaldolase

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Year:  2018        PMID: 30056406

Source DB:  PubMed          Journal:  Dev Period Med


  1 in total

1.  Metabolomic Profiling for Histologically Fibrotic Stage in Chronic Drug-Induced Liver Injury.

Authors:  Xian He; Ming-Xi Zhou; Cheng Cheng; Shan-Shan Li; Yuan Gao; Zhi-Tao Ma; Xin-Hua Song; Zhao-Fang Bai; Zheng-Sheng Zou; Xiao-He Xiao; Jia-Bo Wang; Ya-Wen Lu
Journal:  Front Pharmacol       Date:  2022-05-20       Impact factor: 5.988

  1 in total

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