Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Muscular Dystrophies
Término preferido
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.
Concepto genérico
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
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francés
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Syndrome de Chemke
-
Syndrome de Pagon
-
Syndrome de Warburg
URI
http://data.loterre.fr/ark:/67375/JVR-K3536N0G-D
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