SynthesisInternational journal of molecular sciences2026
Liver Disease in Transaldolase Deficiency: Molecular Basis, Genotype-Phenotype Relationships, and Transplantation Outcomes-A Systematic Review.
Synthesis in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
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Abstract
Transaldolase deficiency (TALDO-D) is an ultra-rare disorder of the non-oxidative pentose phosphate pathway with prominent liver disease and systemic accumulation of polyols and seven-carbon sugars. We systematically reviewed hepatic manifestations, molecular findings, genotype-phenotype relationships, and liver transplantation (LTx) experience. PubMed/MEDLINE and Europe PMC were searched from inception to 10 August 2026, with citation tracking; supplementary Scopus and Web of Science Core Collection searches were performed on 19 August and 1 September 2026, respectively. Twenty-nine primary clinical reports were included. Individual-patient reconciliation supported 51 genetically/biochemically confirmed patients as the primary analytic set; inclusion of one diagnostically uncertain patient with a homozygous in-frame
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