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Diseases

Genetic and Rare Diseases Information Center (GARD)

Nager acrofacial dysostosis


Other Names for this Disease
  • Mandibulofacial dysostosis, Treacher Collins type, with limb anomalies
  • Nager syndrome
  • AFD, Nager type
  • Preaxial acrofacial dysostosis
  • Nager acrofacial dysostosis syndrome
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Research

Clinical Trials & Research for this Disease

  • The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.

Patient Registry

  • The Genetic Analysis of Limb Malformation Disorders is a research project and patient registry that aims to better understand the cause of congenital contractures. Click on the link above to learn more.

    Genetic Analysis of Limb Malformation Disorders
    Bamshad Laboratory
    University of Washington SOM
    Department of Pediatrics
    Division of Genetics & Developmental Medicine
    1959 NE Pacific St. HSB RR349 B
    Seattle, WA 98195-6320 USA

    Maggie McMillin, Research Study Coordinator
    E-mail: margaret.mcmillin@seattlechildrens.org
    E-mail 2: mcmillin@u.washington.edu
    Phone: 206-221-3849
Other Names for this Disease
  • Mandibulofacial dysostosis, Treacher Collins type, with limb anomalies
  • Nager syndrome
  • AFD, Nager type
  • Preaxial acrofacial dysostosis
  • Nager acrofacial dysostosis syndrome
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.