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21 Heriditary cystatin C amyloid angiopathy (HCCAA): Hereditary cystatin C amyloid angiopathy (HCCAA) is a rare dominantly inherited disease caused by a leucine to glutamine variant of human cystatin C (hCC)
A decade ago, if someone told me we'd be discussing 30% weight loss from a subcutaneous injection, I would have called it fantasy
Other research has found that individuals with folate-related mutations can still have a functional deficiency even when blood levels of folate are within the normal range, [32] and recommended supplementation of methyltetrahydrofolate to potentially prevent and treat dementia (along with depression)
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