Attention and Motor Learning in Adult Patients with Neurofibromatosis Type 1
- PMID: 33978520
- PMCID: PMC8987013
- DOI: 10.1177/10870547211012035
Attention and Motor Learning in Adult Patients with Neurofibromatosis Type 1
Abstract
Objective: Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder that is associated with cognitive disabilities, including attention and motor learning problems. These disabilities have been extensively studied in children with NF1 but limited studies have been performed in adults.
Method: Attention, motor learning and intellectual performance were studied with neuropsychological tasks in 32 adults with NF1 and 32 controls.
Results: The NF1 and control group performed similarly on attention and motor learning tasks, although controls had shorter reaction times than adults with NF1 during the motor learning task (t[60] = -2.20, p = .03). Measures of attention or motor learning were not significantly associated with reduced intellectual performance in NF1.
Conclusion: In contrast to many studies in children with NF1, our findings did not provide evidence for presence of attention or motor learning problems in adults with NF1 in neuropsychological tasks. Our observations may be of clinical importance to determine treatment focus in adults with NF1.
Keywords: adult; cognition; motor performance; neurofibromatosis type 1; neuropsychological functioning.
Conflict of interest statement
Figures



Similar articles
-
Neuropsychological profile in adults with neurofibromatosis type 1 compared to a control group.J Intellect Disabil Res. 2013 Sep;57(9):874-86. doi: 10.1111/j.1365-2788.2012.01648.x. Epub 2012 Oct 24. J Intellect Disabil Res. 2013. PMID: 23095048
-
The nature and frequency of cognitive deficits in children with neurofibromatosis type 1.Neurology. 2005 Oct 11;65(7):1037-44. doi: 10.1212/01.wnl.0000179303.72345.ce. Neurology. 2005. PMID: 16217056
-
The impact of ADHD on the cognitive and academic functioning of children with NF1.Dev Neuropsychol. 2012;37(7):590-600. doi: 10.1080/87565641.2012.695831. Dev Neuropsychol. 2012. PMID: 23066937
-
Neurocognitive dysfunction in children with neurofibromatosis type 1.Curr Neurol Neurosci Rep. 2003 Mar;3(2):129-36. doi: 10.1007/s11910-003-0064-3. Curr Neurol Neurosci Rep. 2003. PMID: 12583841 Review.
-
Molecular and cellular mechanisms of learning disabilities: a focus on NF1.Annu Rev Neurosci. 2010;33:221-43. doi: 10.1146/annurev-neuro-060909-153215. Annu Rev Neurosci. 2010. PMID: 20345245 Free PMC article. Review.
Cited by
-
Gender-Specific Fine Motor Skill Learning Is Impaired by Myelin-Targeted Neurofibromatosis Type 1 Gene Mutation.Cancers (Basel). 2024 Jan 23;16(3):477. doi: 10.3390/cancers16030477. Cancers (Basel). 2024. PMID: 38339230 Free PMC article.
-
Neurocognitive functioning in adults with neurofibromatosis type 1- a nationwide population-based study.Orphanet J Rare Dis. 2024 Nov 28;19(1):441. doi: 10.1186/s13023-024-03454-w. Orphanet J Rare Dis. 2024. PMID: 39609892 Free PMC article.
-
Diverse learners: learning disabilities and quality of life following mind-body and health education interventions for adults with neurofibromatosis.J Neurooncol. 2024 Apr;167(2):315-322. doi: 10.1007/s11060-024-04610-9. Epub 2024 Feb 27. J Neurooncol. 2024. PMID: 38409461 Free PMC article.
-
A systematic review and meta-analysis of intellectual, neuropsychological, and psychoeducational functioning in neurofibromatosis type 1.Am J Med Genet A. 2022 Aug;188(8):2277-2292. doi: 10.1002/ajmg.a.62773. Epub 2022 May 12. Am J Med Genet A. 2022. PMID: 35546306 Free PMC article.
-
Cerebellum-dependent associative learning is not impaired in a mouse model of neurofibromatosis type 1.Sci Rep. 2022 Nov 9;12(1):19041. doi: 10.1038/s41598-022-21429-4. Sci Rep. 2022. PMID: 36351971 Free PMC article.
References
-
- Baudou E., Nemmi F., Biotteau M., Maziero S., Assaiante C., Cignetti F., Vaugoyeau M., Audic F., Peran P., Chaix Y. (2020). Are morphological and structural MRI characteristics related to specific cognitive impairments in neurofibromatosis type 1 (NF1) children? European Journal of Paediatric Neurology, 28, 89–100. 10.1016/j.ejpn.2020.07.003 - DOI - PubMed
-
- Biotteau M., Déjean S., Lelong S., Iannuzzi S., Faure-Marie N., Castelnau P., Rivier F., Lauwers-Cancès V., Baudou E., Chaix Y. (2020). Sporadic and familial variants in NF1: An explanation of the wide variability in neurocognitive phenotype? Frontiers in Neurology, 11, 368. 10.3389/fneur.2020.00368 - DOI - PMC - PubMed
-
- Biotteau M., Tournay E., Baudou E., Destarac S., Iannuzzi S., Faure-Marie N., Castelnau P., Schweitzer E., Rodriguez D., Kemlin I., Dorison N., Rivier F., Carneiro M., Preclaire E., Barbarot S., Lauwers-Cancès V., Chaix Y. (2021). Reading comprehension impairment in children with neurofibromatosis type 1 (NF1): The need of multimodal assessment of attention. Journal of Child Neurology, 883073820981270. 10.1177/0883073820981270 - DOI - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous