Familial Hemifacial Spasm - Case Report -

가족성 편측안면경련 - 증 례 보 고 -

  • Chung, Seung Young (Department of Hemifacial Spasm and Pain Clinic, Department of Neurosurgery, School of Medicine, Kyung-Hee University) ;
  • Rhee, Bong Arm (Department of Hemifacial Spasm and Pain Clinic, Department of Neurosurgery, School of Medicine, Kyung-Hee University) ;
  • Lim, Young Jin (Department of Hemifacial Spasm and Pain Clinic, Department of Neurosurgery, School of Medicine, Kyung-Hee University) ;
  • Kim, Tae Sung (Department of Hemifacial Spasm and Pain Clinic, Department of Neurosurgery, School of Medicine, Kyung-Hee University) ;
  • Kim, Gook Ki (Department of Hemifacial Spasm and Pain Clinic, Department of Neurosurgery, School of Medicine, Kyung-Hee University) ;
  • Leem, Won (Department of Hemifacial Spasm and Pain Clinic, Department of Neurosurgery, School of Medicine, Kyung-Hee University)
  • 정승영 (경희대학교 의과대학 신경외과학교실, 안면 경련 및 통증 크리닉) ;
  • 이봉암 (경희대학교 의과대학 신경외과학교실, 안면 경련 및 통증 크리닉) ;
  • 임영진 (경희대학교 의과대학 신경외과학교실, 안면 경련 및 통증 크리닉) ;
  • 김태성 (경희대학교 의과대학 신경외과학교실, 안면 경련 및 통증 크리닉) ;
  • 김국기 (경희대학교 의과대학 신경외과학교실, 안면 경련 및 통증 크리닉) ;
  • 임언 (경희대학교 의과대학 신경외과학교실, 안면 경련 및 통증 크리닉)
  • Received : 2001.09.05
  • Accepted : 2001.12.03
  • Published : 2001.12.31

Abstract

The authors report two cases of familial hemifacial spasm according to the clinical and three dimensional shortrange magnetic resonance angiography(3D-SRMRA) findings. In the family of the first case, there were five patient's with acquired hemifacial spasm in successive generations. Three male and two female patients in successive generations of the same family developed acquired hemifacial spasm. Four patients were on the left side and one was on the right side. In the family of the second case, there were three patient's with acquired hemifacial spasm in successive generations. Two brothers developed left-sided hemifacial spasm. 3D-SRMRA finding of the probands demonstrated that both anterior inferior cerebellar artery in first case and anterior inferior cerebellar artery & vertebral artery in second case offend the 7th cranial nerve respectively. The presence of familial clustering of these rare disorders suggest an underlying genetic predisposition. All family pedigrees suggest that a pattern of autosomal-dominant inheritance with partial penetrance.

Keywords