"Neurofibromatoses" 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 an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)
| Descriptor ID |
D017253
|
| MeSH Number(s) |
C04.557.580.600.580.590 C04.700.645 C10.562.600 C10.574.500.549 C16.320.400.560 C16.320.700.645
|
| Concept/Terms |
Neurofibromatoses- Neurofibromatoses
- Neurofibromatosis
- Neurofibromatosis Syndrome
- Neurofibromatosis Syndromes
- Syndrome, Neurofibromatosis
- Syndromes, Neurofibromatosis
- Multiple Neurofibromas
- Multiple Neurofibroma
- Neurofibroma, Multiple
- Neurofibromas, Multiple
Neurofibromatosis 3- Neurofibromatosis 3
- Neurofibromatosis 3s
- Neurofibromatosis Type 3
- Neurofibromatosis Type 3s
- Type 3, Neurofibromatosis
|
Below are MeSH descriptors whose meaning is more general than "Neurofibromatoses".
Below are MeSH descriptors whose meaning is more specific than "Neurofibromatoses".
This graph shows the total number of publications written about "Neurofibromatoses" by people in this website by year, and whether "Neurofibromatoses" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 0 | 1 | 1 |
| 2007 | 2 | 0 | 2 |
| 2016 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Neurofibromatoses" by people in Profiles.
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Helenius IJ, Sponseller PD, Mackenzie W, Odent T, Dormans JP, Asghar J, Rathjen K, Pahys JM, Miyanji F, Hedequist D, Phillips JH. Outcomes of Spinal Fusion for Cervical Kyphosis in Children with Neurofibromatosis. J Bone Joint Surg Am. 2016 Nov 02; 98(21):e95.
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Ilyas AM, Nourissat G, Jupiter JB. Segmental neurofibromatosis of the hand and upper extremity: a case report. J Hand Surg Am. 2007 Dec; 32(10):1538-42.
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Farrell CJ, Plotkin SR. Genetic causes of brain tumors: neurofibromatosis, tuberous sclerosis, von Hippel-Lindau, and other syndromes. Neurol Clin. 2007 Nov; 25(4):925-46, viii.
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Graif M, Martinoli C, Rochkind S, Blank A, Trejo L, Weiss J, Kessler A, Derchi LE. Sonographic evaluation of brachial plexus pathology. Eur Radiol. 2004 Feb; 14(2):193-200.