Category: Endocrine & Metabolic / Disorders of Carbohydrate Metabolism
Galactosemia is a rare inherited metabolic disorder in which the body is unable to metabolize the sugar galactose, leading to its accumulation and causing severe damage to organs if untreated.
Estimated at 1 in 30,000 to 1 in 60,000 live births (source: National Organization for Rare Disorders).
Discover the latest clinical trials and treatments for Galactosemia on JourneyForHealth.
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