 Walker-Warburg Syndrome
"Walker-Warburg Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D058494
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| MeSH Number(s) |
C10.500.507.249.249.500 C11.270.881 C16.131.666.507.186.249.500 C16.320.577.750
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| Concept/Terms |
Walker-Warburg Syndrome- Walker-Warburg Syndrome
- Syndrome, Walker-Warburg
- Walker Warburg Syndrome
- Warburg Syndrome
- Syndrome, Warburg
- Chemke Syndrome
- Syndrome, Chemke
Muscle-Eye-Brain Disease- Muscle-Eye-Brain Disease
- Muscle-Eye-Brain Diseases
- MEB (Muscle-Eye-Brain) Syndrome
- Muscle Eye Brain Disease
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Below are MeSH descriptors whose meaning is more general than "Walker-Warburg Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Walker-Warburg Syndrome".
This graph shows the total number of publications written about "Walker-Warburg Syndrome" by people in UAMS Profiles by year, and whether "Walker-Warburg Syndrome" was a major or minor topic of these publications.
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Below are the most recent publications written about "Walker-Warburg Syndrome" by people in Profiles over the past ten years.
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