"Usher Syndromes" 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.
Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable.
Descriptor ID |
D052245
|
MeSH Number(s) |
C09.218.458.341.186.500.500 C09.218.458.341.887.886 C10.597.751.418.341.186.500.500 C10.597.751.418.341.887.886 C10.597.751.941.162.625.500 C11.768.585.658.500.813 C11.966.075.375.500 C16.131.077.299.500 C16.320.290.684.500 C23.888.592.763.393.341.887.886
|
Concept/Terms |
Usher Syndromes- Usher Syndromes
- Syndrome, Usher
- Syndromes, Usher
- Usher Syndrome
- Usher's Syndrome
- Syndrome, Usher's
- Ushers Syndrome
- Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
- Dystrophia Retinae Pigmentosa Dysostosis Syndrome
- Graefe-Usher Syndrome
- Graefe Usher Syndrome
- Syndrome, Graefe-Usher
- Hallgren Syndrome
- Syndrome, Hallgren
- Retinitis Pigmentosa-Deafness Syndrome
- Retinitis Pigmentosa Deafness Syndrome
- Retinitis Pigmentosa-Deafness Syndromes
- Syndrome, Retinitis Pigmentosa-Deafness
- Syndromes, Retinitis Pigmentosa-Deafness
- Deafness-Retinitis Pigmentosa Syndrome
- Deafness Retinitis Pigmentosa Syndrome
- Deafness-Retinitis Pigmentosa Syndromes
- Pigmentosa Syndromes, Deafness-Retinitis
- Syndrome, Deafness-Retinitis Pigmentosa
- Syndromes, Deafness-Retinitis Pigmentosa
Usher Syndrome, Type I- Usher Syndrome, Type I
- Usher Syndrome, Type 1A
- Retinitis Pigmentosa And Congenital Deafness
- Usher Syndrome, Type 1
- Usher Syndrome, Type I, French Variety
|
Below are MeSH descriptors whose meaning is more general than "Usher Syndromes".
Below are MeSH descriptors whose meaning is more specific than "Usher Syndromes".
This graph shows the total number of publications written about "Usher Syndromes" by people in this website by year, and whether "Usher Syndromes" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2017 | 1 | 0 | 1 |
2018 | 2 | 0 | 2 |
2019 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Usher Syndromes" by people in Profiles.
-
Novel USH1G homozygous variant underlying USH2-like phenotype of Usher syndrome. Eur J Ophthalmol. 2021 Mar; 31(2):NP18-NP22.
-
Genetic screening of Russian Usher syndrome patients toward selection for gene therapy. Ophthalmic Genet. 2018 12; 39(6):706-713.
-
Central Retina Functional Damage in Usher Syndrome Type 2: 22 Years of Focal Macular ERG Analysis in a Patient Population From Central and Southern Italy. Invest Ophthalmol Vis Sci. 2018 08 01; 59(10):3827-3835.
-
Usher syndrome and late-onset psychosis. Australas Psychiatry. 2017 06; 25(3):316.