Format:
Online-Ressource
ISSN:
1875-9041
Content:
Abstract: Joubert syndrome (JS) is a rare autosomal recessive disorder. All patients affected by this syndrome presented a characteristic picture of cranial fossa malformations, called “molar tooth sign.” This sign is defined by the presence in axial section at the level of a deck/midbrain, of hypo/dysplasia of the cerebellar vermis, abnormally deep interpeduncular fossa and horizontalized thickened and elongated superior cerebellar peduncles. Although “molar tooth sign” is peculiar of JS, other radiological findings have been also reported in these patients. Here, the authors briefly assumed the principal magnetic resonance imaging findings of JS.
In:
volume:21
In:
number:01
In:
year:2023
In:
pages:073-077
In:
Journal of pediatric neurology, [New York] : Thieme Publishers New York, 2003-, 21, Heft 01 (2023), 073-077, 1875-9041
Language:
English
DOI:
10.1055/s-0042-1760241
URN:
urn:nbn:de:101:1-2023030910371444555214
URL:
https://doi.org/10.1055/s-0042-1760241
URL:
https://nbn-resolving.org/urn:nbn:de:101:1-2023030910371444555214
URL:
https://d-nb.info/1282902954/34