"Sotos 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.
Congenital or postnatal overgrowth syndrome most often in height and occipitofrontal circumference with variable delayed motor and cognitive development. Other associated features include advanced bone age, seizures, NEONATAL JAUNDICE; HYPOTONIA; and SCOLIOSIS. It is also associated with increased risk of developing neoplasms in adulthood. Mutations in the NSD1 protein and its HAPLOINSUFFICIENCY are associated with the syndrome.
| Descriptor ID |
D058495
|
| MeSH Number(s) |
C16.131.077.889 C16.131.260.905 C16.320.180.905
|
| Concept/Terms |
Sotos Syndrome- Sotos Syndrome
- Syndrome, Sotos
- Sotos Sequence
- Sequence, Sotos
- Sotos' Syndrome
- Soto Syndrome
- Soto's Syndrome
- Syndrome, Sotos'
- Cerebral Gigantism
- Cerebral Gigantisms
- Gigantism, Cerebral
- Gigantisms, Cerebral
|
Below are MeSH descriptors whose meaning is more general than "Sotos Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Sotos Syndrome".
This graph shows the total number of publications written about "Sotos Syndrome" by people in this website by year, and whether "Sotos Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Sotos Syndrome" by people in Profiles.
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COVID-19 pneumonia in a child with Sotos syndrome. Pediatr Int. 2021 10; 63(10):1247-1249.
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COVID-19 and social responsiveness: A comparison between children with Sotos syndrome and autism. Psychiatry Res. 2021 05; 299:113851.
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Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New "c.[5867T>A]+[=]"; "p.[Leu1956Gln]+[=]" NSD1 Missense Mutation and Complex Skin Hamartoma. Int J Mol Sci. 2018 Oct 16; 19(10).