McCauley SM, Kim K, Nowosielska A, Dauphin A, Yurkovetskiy L, Diehl WE, et al
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)
Iron deficiency may present with anemia, fatigue, pallor, and increased risk of infections
It is a dietary supplement for immune support, skin health, and energy
Capsules underwent microbiological safety testing at ALS Laboratories (UK) before use
The use of compounded Vitamin B12 preparations like Tiaminal B12 injection allows for a more nuanced approach to patient care, addressing individual nutritional deficiencies and health status. Dr