Harvard Catalyst Profiles

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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.


This graph shows the total number of publications written about "Walker-Warburg Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Walker-Warburg Syndrome" was a major or minor topic of these publication.
Bar chart showing 8 publications over 5 distinct years, with a maximum of 2 publications in 2011 and 2013 and 2018
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.