Lowe Syndrome Association (LSA)
The Lowe Syndrome Association (LSA) is an international non-profit organization made up of families, friends and professionals dedicated to helping children with Lowe Syndrome and their families. Its main purposes are to foster communication among families, provide information and support research.
- 972 733 1338
- PO Box 864346
United States of America
LSA Medical Research GrantVaries, approx. US$30,000Closes: Varies