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Transaldolase deficiency is an autosomal recessive disorder resulting from inherited mutations in the TALDO1 gene

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Patients should discuss with their GP whether they might be eligible for NHS provision through specialist services, though realistic expectations about waiting times and strict eligibility criteria are important

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Ro Body Program includes provider access, lab testing, and robust insurance navigation in one membership but doesnt offer oral or non-GLP-1 meds and provides less intensive support tools

The levocarnitine addition does not fundamentally change this decision calculus