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MRI abnormalities in neurofibromatosis type 1 (NF1): a study of men and mice.
- Source :
-
Brain & development [Brain Dev] 1999 Jun; Vol. 21 (4), pp. 268-73. - Publication Year :
- 1999
-
Abstract
- Hyperintense lesions on T2-weighted MR images of the brain, predominantly located in the basal ganglia, the brainstem and cerebellum, are a frequent finding in patients with neurofibromatosis type 1. Nature and significance of these lesions are still unknown so that the term 'unidentified bright objects' (UBOs) has been introduced to allow an unbiased description. We analyzed brain MRI scans of 31 children with definite diagnosis of neurofibromatosis type 1 according to the NIH criteria. High-intensity lesions on T2-weighted images were present in 86% of the patients. They did not correlate to other MRI findings such as optic pathway gliomas and were not indicative of intellectual impairment. Additionally, brain MR imaging of Nf1 knockout mice was performed to find out if similar abnormalities are present in this animal model. A total of 9 Nf1 knockout mice was examined on a dedicated animal MRI scanner at 4.7 Tesla but no evidence of high-signal intensity lesions on T2-weighted images was found. Therefore, the Nf1 mouse model seems to be unhelpful in providing further insights into the histological basis of hyperintense MRI abnormalities in NF1 patients.
- Subjects :
- Adolescent
Animals
Child
Child, Preschool
Developmental Disabilities diagnosis
Female
Gene Deletion
Genes, Neurofibromatosis 1 genetics
Humans
Infant
Infant, Newborn
Magnetic Resonance Imaging
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Neurofibromatosis 1 genetics
Seizures diagnosis
Brain Neoplasms diagnosis
Glioma diagnosis
Neurofibromatosis 1 diagnosis
Optic Nerve Neoplasms diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 0387-7604
- Volume :
- 21
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Brain & development
- Publication Type :
- Academic Journal
- Accession number :
- 10392751
- Full Text :
- https://doi.org/10.1016/s0387-7604(99)00024-8