Oculocerebrorenal syndrome

Oculocerebrorenal syndrome of Lowe (OCRL) is a multisystem disorder characterized by congenital cataracts, glaucoma, intellectual disabilities, postnatal growth retardation and renal tubular dysfunction with chronic renal failure.

Also known as: Lowe disease, Lowe oculo-cerebro-renal syndrome, Lowe oculocerebrorenal syndrome, Lowe syndrome, Lowe syndrome, X-linked recessive, OCR, OCRL, oculo-cerebro-renal dystrophy

4 clinical trials for this condition and its sub-types, 3 tagged with Oculocerebrorenal syndrome itself.