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Walker-Warburg Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • Rare autosomal recessive lissencephaly type 2 associated with congenital MUSCULAR DYSTROPHY and eye anomalies (e.g., RETINAL DETACHMENT; CATARACT; MICROPHTHALMOS). It is often associated with additional brain malformations such as HYDROCEPHALY and cerebellar hypoplasia and is the most severe form of the group of related syndromes (alpha-dystroglycanopathies) with common congenital abnormalities in the brain, eye and muscle development.

Etiquetas alternativas

  • Cerebroocular Dysplasia-Muscular Dystrophy Syndrome
  • Chemke Syndrome
  • COD-MD Syndrome
  • HARD Syndrome
  • Hydrocephalus, Agyria, And Retinal Dysplasia
  • Pagon Syndrome
  • Warburg Syndrome

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-K3536N0G-D

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RDF/XML TURTLE JSON-LD Creado 25/6/10, última modificación 30/6/21