Anterior mesencephalic cap dysplasia: Novel brain stem malformative features associated with joubert syndrome

F. Arrigoni, R. Romaniello, D. Peruzzo, A. D. De Luca, C. Parazzini, E. M. Valente, R. Borgatti, F. Triulzi

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

15 Citaten (Scopus)

Samenvatting

In Joubert syndrome, the "molar tooth" sign can be associated with several additional supra-And infratentorial malformations. Here we report on 3 subjects (2 siblings, 8-14 years of age) with Joubert syndrome, showing an abnormal thick bulging of the anterior profile of the mesencephalon causing a complete obliteration of the interpeduncular fossa. DTI revealed that the abnormal tissue consisted of an ectopic white matter tract with a laterolateral transverse orientation. Tractographic reconstructions support the hypothesis of impaired axonal guidance mechanisms responsible for the malformation. The 2 siblings were compound heterozygous for 2 missense variants in the TMEM67 gene, while no mutations in a panel of 120 ciliary genes were detected in the third patient. The name "anterior mesencephalic cap dysplasia," referring to the peculiar aspect of the mesencephalon on sagittal MR imaging, is proposed for this new malformative feature.

Originele taal-2Engels
Pagina's (van-tot)2385-2390
Aantal pagina's6
TijdschriftAmerican Journal of Neuroradiology
Volume38
Nummer van het tijdschrift12
DOI's
StatusGepubliceerd - 1 dec. 2017
Extern gepubliceerdJa

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