Kulkarni M L, Kannan B, Mathadh Prakash
Department of Pediatrics, JJMMC, Davangere, Karnataka, India.
Indian J Pediatr. 2006 Dec;73(12):1109-11. doi: 10.1007/BF02763057.
Hyperekplexia is a rare, hereditary, non-epileptic disorder characterized by an exaggerated startle reaction to unexpected auditory, somatosensory and visual stimuli. The authors describe a one-day-old term neonate, who presented with jitteriness and episodic tonic spasms, and his elder sister with hyperekplexia. Hyperekplexia though is a rare disorder is one of the differential diagnoses for refractory tonic spasms in infancy. The prognosis is generally good in hereditary hyperekplexia. Recent molecular studies have revealed many associated mutations in the glycine receptor alpha and beta subunit genes.
僵人综合征是一种罕见的遗传性非癫痫性疾病,其特征为对意外的听觉、躯体感觉和视觉刺激出现夸张的惊吓反应。作者描述了一名足月出生一天的新生儿,该新生儿表现出易激惹和发作性强直性痉挛,以及他患有僵人综合征的姐姐。僵人综合征虽然是一种罕见疾病,但却是婴儿期难治性强直性痉挛的鉴别诊断之一。遗传性僵人综合征的预后通常良好。最近的分子研究揭示了甘氨酸受体α和β亚基基因中的许多相关突变。