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39 TPI deficiency (OMIM 190450) is a relatively rare autosomal recessive multisystem disorder, characterized by hemolytic anemia, severe neuromuscular defects, increased susceptibility to infection, and cardiomyopathy.48,134,161 Patients usually die in childhood, although intriguing exceptions have been reported
Some people report subjective changes, while others feel no benefit or experience nausea, pressure, cramping, headache, dizziness, or fatigue
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Understanding the mechanisms behind this effect is essential for clinicians and patients alike
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