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Lowe syndrome (LS) is a rare, X‐linked disorder characterised by numerous symptoms affecting the brain, the eyes, and the kidneys. It is caused by mutations in the oculocerebrorenal syndrome of Lowe (OCRL) protein, a 5‐phosphatase localised in different cellular compartments that dephosphorylates phosphatidylinositol‐4,5‐bisphosphate into phosphatidylinositol‐4‐monophosphate. Some patients with LS...