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Lowe syndrome

Background

Lowe syndrome: Oculo-Cerebro-Renal syndrome

Lowe syndrome was first described by Doctors Lowe, Terrey, and MacLachlan in 1952. It is a rare, inherited, progressive, metabolic disease affecting the eyes, brain and kidneys. Lowe syndrome affects boys of all ethnic groups. The majority of female carriers of the syndrome show the characteristic ophthalmic findings in the lens of each eye. The incidence of Lowe syndrome is thought to be a few per one hundred thousand births but currently there is no accurate data.

What are the symptoms? View What are the symptoms?

Medical text written October 2005 by Contact a Family. Approved October 2005 by Dr A Norden, Consultant in Chemical Pathology, Addenbrooke's Hospital, Cambridge, UK.

 

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