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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Muscular Dystrophies > Walker-Warburg Syndrome
... > Nervous System Diseases > Neuromuscular Diseases > Muscular Diseases > Muscular Disorders, Atrophic > Muscular Dystrophies > Walker-Warburg Syndrome
Musculoskeletal Diseases > Muscular Diseases > Muscular Disorders, Atrophic > Muscular Dystrophies > Walker-Warburg Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Walker-Warburg Syndrome
Eye Diseases > Eye Diseases, Hereditary > Walker-Warburg Syndrome
... > Nervous System Diseases > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group II > Lissencephaly > Cobblestone Lissencephaly > Walker-Warburg Syndrome
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group II > Lissencephaly > Cobblestone Lissencephaly > Walker-Warburg Syndrome

Preferred term

Walker-Warburg Syndrome  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

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

Scope note

  • 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.

History note

  • 2011

In other languages

URI

http://www.yso.fi/onto/mesh/D058494

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