 Neurocutaneous Syndromes
"Neurocutaneous 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.
A group of disorders characterized by ectodermal-based malformations and neoplastic growths in the skin, nervous system, and other organs.
| Descriptor ID |
D020752
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| MeSH Number(s) |
C10.562 C16.131.077.350.712 C16.131.831.350.712 C16.320.850.250.712 C17.800.804.350.712 C17.800.827.250.712
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| Concept/Terms |
Neurocutaneous Syndromes- Neurocutaneous Syndromes
- Neurocutaneous Syndrome
- Syndrome, Neurocutaneous
- Syndromes, Neurocutaneous
- Phacomatosis
- Phakomatosis
- Neurocutaneous Disorders
- Neurocutaneous Disorder
- Phacomatoses
- Neuroectodermal Dysplasia Syndromes
- Neuroectodermal Dysplasia Syndrome
- Syndrome, Neuroectodermal Dysplasia
- Syndromes, Neuroectodermal Dysplasia
- Phakomatoses
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Below are MeSH descriptors whose meaning is more general than "Neurocutaneous Syndromes".
Below are MeSH descriptors whose meaning is more specific than "Neurocutaneous Syndromes".
This graph shows the total number of publications written about "Neurocutaneous Syndromes" by people in UAMS Profiles by year, and whether "Neurocutaneous 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 |
|---|
| 2019 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Neurocutaneous Syndromes" by people in Profiles over the past ten years.
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Samanta D, Schaefer B. Mosaic chromosome 5p tetrasomy: eye closure-induced seizures in a rare neurocutaneous syndrome. Acta Neurol Belg. 2020 Jun; 120(3):713-716.
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Bavle A, Shah R, Gross N, Gavula T, Ruiz-Elizalde A, Wierenga K, McNall-Knapp R. Encephalocraniocutaneous Lipomatosis. J Pediatr Hematol Oncol. 2018 10; 40(7):553-554.
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Knight Johnson A, Schaefer GB, Lee J, Hu Y, Del Gaudio D. Alu-mediated deletion of PIGL in a Patient with CHIME syndrome. Am J Med Genet A. 2017 May; 173(5):1378-1382.
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Samanta D, Bosanko KB, Zarate YA. An infant with ash-leaf and caf? au lait spots: a case of double phakomatosis. Acta Neurol Belg. 2017 03; 117(1):323-324.
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