Literature DB >> 29962440

[A pedigree of hereditary hyperekplexia].

Hideyuki Moriyoshi1,2, Yukiko Hata3, Ryosuke Inagaki1, Junichiro Suzuki1, Suguru Nishida1, Naoki Nishida3, Yasuhiro Ito1.   

Abstract

A 31-year old women presented with excessive startle reflex and frequent falls. Her startle reflex is induced by slight stimuli which are not problematic in most people. Soon after her startle reflex is evoked, generalized muscle stiffness occurs. She becomes rigid and falls down without loss of consciousness. Because she cannot protect herself when she is startled and falls, she has repeatedly bruised her head and face. The pedigree includes her father and two sisters with similar symptoms. Gene analysis revealed GLRA1 mutation, and she was diagnosed with hereditary hyperekplexia (HPX). Symptoms improved with clonazepam 1 mg/day. HPX patients live with severe anxiety about frequent falls and sometimes suffer serious injury, such as cerebral concussion or bone fracture. Although HPX might sometimes be underestimated, accurate diagnosis is very important for effective treatment.

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Keywords:  Fall; GLRA1; Glycine receptor; Hyperekplexia; Startle disease

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Year:  2018        PMID: 29962440     DOI: 10.5692/clinicalneurol.cn-001129

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN: 0009-918X


  1 in total

1.  C.292G>A, a novel glycine receptor alpha 1 subunit gene (GLRA1) mutation found in a Chinese patient with hyperekplexia: A case report.

Authors:  Yan Zhang; Ling-Ling Wu; Xiao-Lan Zheng; Cai-Mei Lin
Journal:  Medicine (Baltimore)       Date:  2020-04       Impact factor: 1.817

  1 in total

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