Quiz Symposium 9. White matter and oligodendrocyte pathology: new insights in neurodevelopmental diseases and epilepsy

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QUIZ QUESTIONS AS SUBMITTED BY THE INVITED SPEAKERS

1) What is the genetic cause of Vanishing White Matter: *

1 point

A) Mutation in GFAP

B) Mutations in any of the Tubulin genes

C) Mutations in any of the genes encoding the subunits of the eukaryotic translation initiation factor 2B

D) Mutations in the CSF1R gene

2) How is the diagnosis of vanishing White Matter established: *

1 point

A) MRI characteristic pattern and genetic testing

B) Neurophysiology (EEG, evoked potentials)

C) Biochemical testing on cultured fibroblasts

D) Whole exome sequencing

3) What is indicated by the 'transmantle sign'? *

1 point

A) An artefact

B) A funnel-shaped area of hypomyelination

C) Consistency with all FCDs

D) Abnormal vessels

4) What is the role of mTOR in myelination? *

1 point

A) None, myelination is independent of mTOR

B) To provide energy supply via insulin

C) To promote oligodendroglial migration

D) To promote myelination

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