1. Joubert syndrome: congenital cerebellar ataxia with the molar tooth
Marta Romani, PhD, Alessia Micalizzi, BSc, Prof Enza Maria Valente, MD 
The Lancet Neurology 
Volume 12, Issue 9, Pages (September 2013)
DOI: /S (13)
Copyright © 2013 Elsevier Ltd Terms and Conditions

2. Figure 1
Neuroimaging findings in a 2-year-old child with pure Joubert syndrome (upper panels) compared with a healthy control child (lower panels)
(A) Midsagittal T1-weighted image shows a moderate hypoplasia and dysplasia of the cerebellar vermis (arrows) with secondary distortion and enlargement of the fourth ventricle with rostral shifting of the fastigium (arrowhead). A deepened interpeduncular fossa is also noted (asterisk). (B) Parasagittal T1-weighted image shows the thickened, elongated, and horizontally orientated superior cerebellar peduncles (arrow). (C) Axial T1-weighted image at the pontomesencephalic junction shows the molar tooth sign with a deepened interpeduncular fossa (arrowhead) and elongated, thickened, and horizontally orientated superior cerebellar peduncles (arrows). Additionally, the cerebellar vermis seems to be hypoplastic and its remnants dysplastic. (D) Coronal T1-weighted image reveals the thickened superior cerebellar peduncles (arrows).
The Lancet Neurology  , DOI: ( /S (13) )
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3. Figure 2
Schematic representation of the structure of the primary cilium and its protein complexes
Most proteins that are mutated in Joubert syndrome and Meckel syndrome cluster in large complexes at the basal body or the transition zone of the cilium. These complexes participate in the regulation of ciliogenesis, control the trafficking of specific pools of molecules targeted to the cilium, and are implicated in signalling pathways mediated by the cilium. Other Joubert syndrome proteins are also found along the ciliary axoneme or interact with Shh or Wnt pathways, which have crucial roles in embryonic development. IFT=intraflagellary transport.
The Lancet Neurology  , DOI: ( /S (13) )
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4. Figure 3
Range of organ involvement in Joubert syndrome and classification in clinical subgroups (in bold)
Chorioretinal colobomas are found more frequently in the subgroup of patients with Joubert syndrome with liver involvement, but can also be present in other subgroups. Similarly, polydactyly (especially pre-axial or meso-axial) is invariably present in the orofaciodigital type VI subgroup, but post-axial polydactyly is also frequently reported in association with other Joubert syndrome phenotypes. Other clinical features outside the circles occur rarely, without a specific association with a clinical subgroup. COR=cerebello-ocolo-renal. OFDVI=orofaciodigital type VI syndrome.
The Lancet Neurology  , DOI: ( /S (13) )
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