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Hereditary folate malabsorption Hereditary folate malabsorption is caused by mutations in the SLC46A1 gene coding for the folate transporter PCFT and typically affects gastrointestinal folate absorption and folate transport into the brain (183)

Noom Med offers multiple medication pathways, including: Every pathway is integrated with Nooms core strength: evidence-based behavior change

The global obesity GLP-1 market is valued at USD 8,169 million in 2025

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As the prevalence of endometriosis continues to rise, particularly among young women, the need for effective interventions becomes increasingly urgent