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J Korean Neurol Assoc. 1995;13(3):651-656.
- Neuroacanthocytosis : 2 Cases of Familial Choreoacanthocytosis
Neuroacanthocytosis : 2 Cases of Familial Choreoacanthocytosis
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Sang Bock Lee, M.D., Soo Chul Park, M.D., Myung Sil Lee, M.D.
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Department of Neurology, Yongdong Severance Hospital Yonsei University, Yonsei University, College of Medicine
- Neuroacanthocytosis :2례의 가족성 Choreoacanthocytosis
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이상복, 박수철, 이명식
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연세대학교 신경과
- Abstract
- Neuroacanthocytosis is a rare dosorder characterized by various neurological manifestations and the presence of abnormal red blood cells called acanthocytes which have a disturbed morphology showing spiky, knobby end projections. Acanthocytosis associated with neurological involvements includes 3 major syndromes ; Bassen-Korzweig syndrome, choreoacanthocytosis (or Levine-Critchley syndrome), and Mcleod syndrome. Here, we report two cases of familial choreoacanthocytosis. A 40 years old man presented with orofacial dyskinesia, involuntary vocalization, dysarthria, dysphagia, generalized choreic movements, hyporef lexia, and amyotrophy of the bilarteral anterior tibilais muscles. Serum creatine phosphokinase was increased. Scanning electronmicroscopic examination of the fresh peripheral blood smear film showed acanthocytes, corresponding to about 6% of all red blood cells. His one of two daughter had high arched foot, bradykinesia, and hypoactive deep tendon reflexes. A 70 years old woman showed head and hand tremor, bilateral eye brow choreic movements, torticollis and bradykinesia. Her mother and two younger sisters had head termor. Serum creatine phosphokinase level was normal. Scanning electronmicroscopic examination of the fresh peripheral blood smear showed acnthocytes, corresponding to 9% of the examined red blood cells.
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