Genetic and imaging features of cerebellar abnormalities in tuberous sclerosis complex: more insights into their pathogenesis

Dev Med Child Neurol. 2018 Jul;60(7):724-725. doi: 10.1111/dmcn.13769.

Authors

Renzo Manara¹, Samuela Bugin², Maria Federica Pelizza², Stefano Sartori², Margherita Nosadini², Francesca Labriola³, Paola Canevini⁴, Aglaia Vignoli⁴, Irene Toldo²

Affiliations

¹ Department of Medicine and Surgery, Neuroradiology, Sezione di Neuroscienze, University of Salerno, Baronissi, Italy.
² Department of Woman and Child Health, Pediatric Neurology and Neurophysiology Unit, University Hospital of Padova, Padova, Italy.
³ Epilepsy and Sleep Medicine Center, Neuropsychiatric Unit, ASST Santi Paolo Carlo, Milan, Italy.
⁴ Epilepsy Center, Health Sciences Department, University of Milano, Milan, Italy.

PMID: 29882962
DOI: 10.1111/dmcn.13769

No abstract available

Publication types

Letter

MeSH terms

Adolescent
Cerebellar Diseases / diagnostic imaging
Cerebellar Diseases / etiology*
Child
Child, Preschool
Female
Humans
Image Processing, Computer-Assisted
Infant
Infant, Newborn
Magnetic Resonance Imaging
Male
Mutation / genetics*
Retrospective Studies
Tuberous Sclerosis Complex 2 Protein
Tuberous Sclerosis* / complications
Tuberous Sclerosis* / diagnostic imaging
Tuberous Sclerosis* / genetics
Tumor Suppressor Proteins / genetics*

Substances

Tuberous Sclerosis Complex 2 Protein
Tumor Suppressor Proteins