The primary purposes of the LSA are to foster communication among families, provide information, and support and encourage medical research. Founded in 1983, the LSA is an international, all-volunteer, non-profit organization made up of parents, friends, professionals, and others who are interested in helping children and young men with Lowe syndrome. Lowe syndrome is a rare genetic condition affecting males that results in multiple disabilities and serious health problems. There is no cure, but many of the symptoms can be treated effectively with medical intervention. With the help of the LSA, researchers have added significantly to the body of knowledge about Lowe syndrome, and parents have benefited greatly from the mutual support and information provided by the organization.