| Literature DB >> 26002775 |
Pedro López Ruiz1, Maria Eugenia García García1, Daniela Dicapua Sacoto1, Alberto Marcos-Dolado1.
Abstract
Joubert syndrome and related disorders comprise a subgroup of ciliopathies defined by the presence of the 'molar tooth sign', a midbrain-hindbrain malformation identifiable by neuroimaging. Characteristically, the corticospinal tract and superior cerebellar peduncles do not decussate. Epileptic seizures are uncommon. We present a case of a 28-year-old man with a background of Leber's congenital amaurosis with nephronophthisis, requiring kidney transplantation, and mental retardation, who developed epileptic seizures consisting of a short muffled cry and involuntary shaking movements of the extremities beginning in the left upper limb; these episodes lasted several seconds and occurred in clusters. Simultaneous video-EEG recording showed an ictal pattern in the left frontal lobe. Brain MRI revealed the pathognomonic 'molar tooth sign'; diffusion tensor imaging (DTI)-tractography showed a lack of decussation of both corticospinal tracts. To the best of our knowledge, this is the first time that DTI-tractography has been used to uncover the anatomical substrate underlying the semiology of epileptic seizures. 2015 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2015 PMID: 26002775 PMCID: PMC4442200 DOI: 10.1136/bcr-2014-207719
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X