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SAO is caused by a deletion, or less commonly a mutation, in SLC4A1 (for solute carrier family 4, anion exchanger, member 1), located on chromosome 17q21-q22

doi: 10.3389/fcell.2022.810327 28 Friedmann AngeliJPXavier da SilvaTNSchillingB

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Combination therapy The scientific rationale for combining 5ARIs and 1 -AR antagonists is based on their different and complementary modes of action, that help in managing static and dynamic component responsible for of an enlarged prostate gland and symptoms of LUTS

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