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Fragile X syndrome is caused by mutations in FMR1 gene (which encodes fragile X mental retardation protein, FMRP) expressed in both neurones and astrocytes

This depletes our physiological resilience and metabolic reserve, and can lead to malfunction [1]

doi: 10.1136/jitc-2021-004378 236 AwwadHMOhlmannCHStoeckleMAzizRGeiselJObeidR

Subcutaneous administration of vitamin B12 is sometimes employed, especially in patients with congenital cobalamin metabolism disorders who require high doses to maintain normal metabolic pathways

The vitamin B-12 injection has been shown to provide these key benefits: boosts energy and overall metabolic rate