Lowe Syndrome

This page has been archived. It has not been updated since 25/08/2011. External links and references may no longer work.

UK sources of information and / or support

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Lowe Syndrome Trust

The main aim of the trust is to initiate interest and raise funding for medical research into Lowe Syndrome.

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Lowe Syndrome

Information from Contact a Family.

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Lowe Syndrome Association

The LSA is an international, voluntary, non-profit organization made up of parents, friends, professionals, and others who are interested in Lowe syndrome, a rare genetic condition that affects boys.


Further sources / more detailed information

Some non-UK sites

The following list popular non-UK health information sites with content aimed at the general public. They are mainly from the US. They have not been checked to see if information about the above topic is included but these large sites are comprehensive.

More detailed medical information

The following list online sources of more detailed medical information, mainly from the UK. These sites are mainly aimed at health professionals, but are of interest to all. They have not been checked to see if information about the above topic is included, but information about most medical topics can usually be found.

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