Resources- Specific Diagnosis Card Catalog- Lowe Syndrome


  • Who to Contact
  • Where to Go to Chat with Others?
  • Learn More About it
  • Links
  • Who to Contact

    Lowe Syndrome Association
    222 Lincoln Street
    West Lafayette IN 47906
    (765) 743-3634
    E-mail: info@lowesyndrome.org
    Web: www.lowesyndrome.org

    The LSA is an international, voluntary, non-profit organization made up of parents, friends, professionals, and others who are interested in Lowe syndrome (LS), a rare genetic condition that affects boys. We've been working since 1983 to develop a community of support and encouragement for families affected by LS.

    Where to Go to Chat with Others

    LSA-Talk
    Share concerns, questions, experiences and advice regarding Lowe syndrome and issues relating to the LSA.

    Learn More About It

    Questions & Answers About Lowe Syndrome

    What is Lowe Syndrome?

    Lowe Syndrome Information
    from OMIM

    Caring for Children's Teeth in Lowe Syndrome

    Links

    Lowe Syndrome Association

    UK Lowe Syndrome Trust

    Lowe Syndrome Mutation Database

    Association du Syndrome de Lowe
    France

    l'Associazione Italiana della Sindrome di Lowe
    Italy

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