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Diseases

Genetic and Rare Diseases Information Center (GARD)

Walker-Warburg syndrome


Other Names for this Disease
  • Hydrocephalus, agyria and retinal dysplasia
  • Hard syndrome
  • Hard +/- E syndrome
  • Warburg syndrome
  • Chemke syndrome
Related Diseases
  • Congenital disorder of glycosylation with developmental anomaly
  • Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies
  • Congenital muscular dystrophy
  • Congenital muscular dystrophy due to dystroglycanopathy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

News & Events


ORDR Co-Sponsored Conferences

  • 2016 Rare Disease Day at NIH, Monday, February 29, 2016
    Location: Building 10, Masur Auditorium, National Institutes of Health, Bethesda, MD
    Description: The 2016 Rare Disease Day at NIH will take place on February 29. The event, sponsored by NCATS and the NIH Clinical Center, aims to raise awareness about rare diseases, the patients they affect and the research collaborations that are addressing rare disease challenges. The day will feature tours, posters and exhibits, and presentations.

  • Congenital Muscular Dystrophy: From Clinical Pathology to Underlying Scientific Mechanisms, Exploring the Role of the Myomatrix, Sunday, April 22, 2012 - Tuesday, April 24, 2012
    Location: University of Nevada School of Medicine, Center for Molecular Medicine, Reno, NV
    Description: The goals of the conference are to: 1) Establish the current state of knowledge in different myomatrix research areas germane to the CMDs and to dystrophic pathology, 2) Explore novel mechanisms, intersections and crosstalk of relevant mechanisms and perform comparative analysis across disease models, 3) Design effective strategies and platforms to pursue treatment development for key aspects of CMD clinical pathology to drive future translational opportunities

Other Names for this Disease
  • Hydrocephalus, agyria and retinal dysplasia
  • Hard syndrome
  • Hard +/- E syndrome
  • Warburg syndrome
  • Chemke syndrome
Related Diseases
  • Congenital disorder of glycosylation with developmental anomaly
  • Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies
  • Congenital muscular dystrophy
  • Congenital muscular dystrophy due to dystroglycanopathy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.