What is Lowe's syndrome?
Lowe syndrome is a rare genetic disorder that primarily affects the eyes, brain and kidneys. Affected children typically have a congenital cataract, developmental delays, muscle weakness and difficulties with kidney function. The disease is caused by mutations in the OCRL gene and predominantly affects boys.
Aids that are frequently used for LOWE syndrome:
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You can find more helpful information about LOWE syndrome here:
www.lowe-syndrom.de