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Sandhoff Disease

"Sandhoff Disease" 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.

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An autosomal recessive neurodegenerative disorder characterized by an accumulation of G(M2) GANGLIOSIDE in neurons and other tissues. It is caused by mutation in the common beta subunit of HEXOSAMINIDASE A and HEXOSAMINIDASE B. Thus this disease is also known as the O variant since both hexosaminidase A and B are missing. Clinically, it is indistinguishable from TAY-SACHS DISEASE.


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This graph shows the total number of publications written about "Sandhoff Disease" by people in this website by year, and whether "Sandhoff Disease" was a major or minor topic of these publications.
Bar chart showing 6 publications over 4 distinct years, with a maximum of 2 publications in 2014 and 2015
To see the data from this visualization as text, click here.
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