"Bardet-Biedl 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.
An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA; POLYDACTYLY; OBESITY; MENTAL RETARDATION; hypogenitalism; renal dysplasia; and short stature. This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME. (From J Med Genet 1997 Feb;34(2):92-8)
| Descriptor ID |
D020788
|
| MeSH Number(s) |
C10.228.140.617.200 C16.131.077.245.125 C16.320.184.125
|
| Concept/Terms |
Bardet-Biedl Syndrome- Bardet-Biedl Syndrome
- Bardet Biedl Syndrome
- Syndrome, Bardet-Biedl
- Laurence-Moon-Bardet-Biedl Syndrome
- Laurence Moon Bardet Biedl Syndrome
- Syndrome, Laurence-Moon-Bardet-Biedl
|
Below are MeSH descriptors whose meaning is more general than "Bardet-Biedl Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Bardet-Biedl Syndrome".
This graph shows the total number of publications written about "Bardet-Biedl Syndrome" by people in this website by year, and whether "Bardet-Biedl Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 |
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Below are the most recent publications written about "Bardet-Biedl Syndrome" by people in Profiles.
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Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary cilia. Clin Genet. 2011 Dec; 80(6):523-31.