| Literature DB >> 29544888 |
Didem Yücel-Yılmaz1, Emrah Yücesan2, Dilek Yalnızoğlu3, Kader Karlı Oğuz4, Mahmut Şamil Sağıroğlu5, Uğur Özbek2, Esra Serdaroğlu3, Başar Bilgiç6, Sevim Erdem7, Sibel Aylin Uğur İşeri2, Haşmet Hanağası6, Hakan Gürvit6, Rıza Köksal Özgül1, Ali Dursun8.
Abstract
Hereditary spastic paraplegias (HSPs) are a group of genetic disorders resulting in pyramidal tract impairment, predominantly in lower limbs. KIF1C gene has recently been identified as one of the genetic causes of HSP and associated with pure or complicated HSP. We present three patients with complicated HSP from two unrelated families, who had early onset progressive cerebellar signs and developed pyramidal tract signs during follow-up. Whole exome sequencing in these patients followed by segregation analysis identified novel truncating KIF1C mutations (c.463C> T; p.R155∗ and c.2478delA; p.Ala828Argfs∗13). Neuroimaging findings showed cerebral and upper cervical spinal atrophy, bilateral symmetrical pyramidal tract involvement, and focal cerebral white matter lesions. Patients with KIF1C mutations may present with cerebellar signs and pyramidal findings may emerge later, therefore complicated HSP should be considered in the differential diagnosis of unidentified cases with cerebellar dysfunction.Entities:
Keywords: Ataxia; Hereditary spastic paraplegia; KIF1C; Kinesin
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Year: 2018 PMID: 29544888 DOI: 10.1016/j.braindev.2018.02.013
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961