Congenital myasthenic syndrome associated with episodic apnea and sudden infant death

被引:53
作者
Byring, RF
Pihko, H
Tsujino, A
Shen, XM
Gustafsson, B
Hackman, P
Ohno, K
Engel, AG
Udd, B
机构
[1] Vaasa Cent Hosp, FIN-65130 Vaasa, Finland
[2] Folkhalsan Fdn, FIN-02510 Helsinki, Finland
[3] Univ Helsinki, Cent Hosp, Hosp Children & Adolescents, FIN-00290 Helsinki, Finland
[4] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
[5] Mayo Clin & Mayo Fdn, Neuromuscular Res Lab, Rochester, MN 55905 USA
[6] Hosp Jakobstad, FIN-68601 Pietarsaari, Finland
[7] Folkhalsan Inst Genet, Biomedicum, Helsinki 00014, Finland
关键词
congenital myasthenic syndrome; episodic apnea; sudden infant death; choline acetyl transferase;
D O I
10.1016/S0960-8966(01)00336-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The sudden infant death syndrome has multiple etiologies. Some congenital myasthenic syndromes can cause sudden infant death syndrome by apnea, but the frequency of this etiology is unknown. We report here a young patient with sudden respiratory crises culminating in apnea followed by recovery, against a background of no or variable myasthenic symptoms without dyspnea. One sib without myasthenic symptoms and one sib who only had mild ptosis died previously during febrile episodes. Studies reported by us elsewhere traced the proband's illness to mutations in choline acetyltransferase. Here, we describe in detail the morphologic investigations and electrophysiologic findings, which point to a presynaptic defect in acetylcholine resynthesis or vesicular tilling, in the proband. Analysis of DNA from a sib who previously died of sudden infant death syndrome revealed the same choline acetyltransferase mutation. Thus, mutations in choline acetyltransferase may be a cause of sudden infant death syndrome as, theoretically, could other presynaptic myasthenic disorders. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:548 / 553
页数:6
相关论文
共 29 条
[1]   Molecular cloning of a human, hemicholinium-3-sensitive choline transporter [J].
Apparsundaram, S ;
Ferguson, SM ;
George, AL ;
Blakely, RD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 276 (03) :862-867
[2]   Changes in the epidemiological pattern of sudden infant death syndrome in southeast Norway, 1984-1998:: implications for future prevention and research [J].
Arnestad, M ;
Andersen, M ;
Vege, Å ;
Rognum, TO .
ARCHIVES OF DISEASE IN CHILDHOOD, 2001, 85 (02) :108-115
[3]   CONGENITAL LAMBERT-EATON MYASTHENIC SYNDROME [J].
BADY, B ;
CHAUPLANNAZ, G ;
CARRIER, H .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1987, 50 (04) :476-478
[4]   FAMILIAL INFANTILE MYASTHENIA-GRAVIS - A PREVENTABLE CAUSE OF SUDDEN-DEATH [J].
BAPTIST, EC ;
LANDES, RV ;
STURMAN, JK .
SOUTHERN MEDICAL JOURNAL, 1985, 78 (02) :201-202
[5]  
Colomer J, 1987, An Esp Pediatr, V26, P457
[6]   FAMILIAL INFANTILE MYASTHENIA-GRAVIS - CAUSE OF SUDDEN-DEATH IN YOUNG CHILDREN [J].
CONOMY, JP ;
LEVINSOHN, M ;
FANAROFF, A .
JOURNAL OF PEDIATRICS, 1975, 87 (03) :428-430
[7]   Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (type Ic) [J].
Donger, C ;
Krejci, E ;
Serradell, AP ;
Eymard, B ;
Bon, S ;
Nicole, S ;
Chateau, D ;
Gary, F ;
Fardeau, M ;
Massoulié, J ;
Guicheney, P .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) :967-975
[8]   CONGENITAL MYASTHENIC SYNDROMES .1. DEFICIENCY AND SHORT OPEN-TIME OF THE ACETYLCHOLINE-RECEPTOR [J].
ENGEL, AG ;
NAGEL, A ;
WALLS, TJ ;
HARPER, CM ;
WAISBURG, HA .
MUSCLE & NERVE, 1993, 16 (12) :1284-1292
[9]   ULTRASTRUCTURAL LOCALIZATION OF ACETYLCHOLINE-RECEPTOR IN MYASTHENIA-GRAVIS AND IN ITS EXPERIMENTAL AUTOIMMUNE MODEL [J].
ENGEL, AG ;
LINDSTROM, JM ;
LAMBERT, EH ;
LENNON, VA .
NEUROLOGY, 1977, 27 (04) :307-315
[10]  
ENGEL AG, 1999, CONT NEUROL SERIES, V56, P251