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Alkaptonuria(HGD) gene analysis Most Popular supporting a more radiant and

Alkaptonuria(HGD) gene analysis Most Popular supporting a more radiant andAlkaptonuria (HGD) Gene Analysis OverviewAlkaptonuria (AKU) is a rare inherited metabolic disorder caused by mutations in the HGD (Homogentisate 1,2 Dioxygenase) gene. These mutations reduce or eliminate the activity of the HGD enzyme, leading to the accumulation of homogentisic acid (HGA) in the body. Excess HGA can cause dark colored urine, pigmentation of connective tissues (ochronosis), joint damage, and other long term complications. What is HGD

SKU: 39901957290 · From southroadsurgery.com.au

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Description

supporting a more radiant and even complexion

Enhanced cellular functioning

Cholestatic liver disease

and overall structure

• Vitamin F supports skin barrier repair and hydration

Alkaptonuria(HGD) gene analysis Most Popular supporting a more radiant andAlkaptonuria (HGD) Gene Analysis OverviewAlkaptonuria (AKU) is a rare inherited metabolic disorder caused by mutations in the HGD (Homogentisate 1,2 Dioxygenase) gene. These mutations reduce or eliminate the activity of the HGD enzyme, leading to the accumulation of homogentisic acid (HGA) in the body. Excess HGA can cause dark colored urine, pigmentation of connective tissues (ochronosis), joint damage, and other long term complications. What is HGD

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