LOWE SYNDROME ASSOCIATION INC
The LSA is an international organization dedicated to helping children with Lowe syndrome and their Founded in 1983, the LSA is an international, non-profit organization made up of parents, friends, professionals, and others who are interested in helping children with Lowe syndrome and their families. Lowe syndrome is a rare genetic condition affecting males that results in multiple physical and medical challenges. There is no cure yet today, but many of the symptoms can be treated effectively. 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.
Founded
1983
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Cincinnati
Lowe Syndrome Association Welcome to your full resource for meaningful information and most importantly help. Family Support Research Medical Answers The Lowe syndrome Association Unites 232 Families 26 Countries 1700 Friends . .
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