Adenylosuccinase deficiency with neonatal onset severe epileptic seizures and sudden death

被引:27
作者
van den Bergh, FAJTM
Bosschaart, AN
Hageman, G
Duran, M
Poll-The, BT
机构
[1] Hosp Med Spectrum Twente, Dept Clin Chem, NL-7500 KA Enschede, Netherlands
[2] Hosp Med Spectrum Twente, Dept Pediat, NL-7500 KA Enschede, Netherlands
[3] Hosp Med Spectrum Twente, Dept Neurol, NL-7500 KA Enschede, Netherlands
[4] Wilhelmina Childrens Hosp, Dept Pediat, Utrecht, Netherlands
关键词
adenylosuccinase deficiency; succinyl purines; purine metabolism; sudden death;
D O I
10.1055/s-2007-973536
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report a male infant with adenylosuccinase deficiency who developed epileptic seizures on the second day of life. Growth was normal and seizures were well controlled with anti-epileptic drugs. Despite axial hypotonia associated with peripheral hypertonicity he presented some development until seven months of age, when he developed high fever and died within a few hours. Although clinical heterogeneity in this disorder of purine synthesis and interconversion is well-known, in 14 out of 17 Eases who experienced epilepsy seizures started after the first year of life. The early presentation in our index patient followed by his sudden death at the age of 7 months has not been described before. A search for disorders of purine metabolism should be included in the screening programme for every child with severe neonatal convulsions.
引用
收藏
页码:51 / 53
页数:3
相关论文
共 15 条
[1]  
BERGH FA, 1992, J INHERIT METAB DIS, V15, P897
[2]   DIAGNOSIS OF INHERITED ADENYLOSUCCINASE DEFICIENCY BY THIN-LAYER CHROMATOGRAPHY OF URINARY IMIDAZOLES AND BY AUTOMATED CATION-EXCHANGE COLUMN CHROMATOGRAPHY OF PURINES [J].
DEBREE, PK ;
WADMAN, SK ;
DURAN, M ;
DEJONGE, HF .
CLINICA CHIMICA ACTA, 1986, 156 (03) :279-287
[3]   Sudden infant death and lysinuric protein intolerance [J].
deKlerk, JBC ;
Duran, M ;
Huijmans, JGM ;
Mancini, GMS .
EUROPEAN JOURNAL OF PEDIATRICS, 1996, 155 (03) :256-257
[4]  
DURAN M, 1994, EUR J PEDIATR, V153, P527
[5]  
HARPEY JP, 1986, LANCET, V2, P1332
[6]   ADENYLOSUCCINASE DEFICIENCY - A NEWLY RECOGNIZED VARIANT [J].
JAEKEN, J ;
VANDENBERGH, F ;
VINCENT, MF ;
CASAER, P ;
VANDENBERGHE, G .
JOURNAL OF INHERITED METABOLIC DISEASE, 1992, 15 (03) :416-418
[7]   ADENYLOSUCCINASE DEFICIENCY - AN INBORN ERROR OF PURINE NUCLEOTIDE SYNTHESIS [J].
JAEKEN, J ;
WADMAN, SK ;
DURAN, M ;
VANSPRANG, FJ ;
BEEMER, FA ;
HOLL, RA ;
THEUNISSEN, PM ;
DECOCK, P ;
VANDENBERGH, F ;
VINCENT, MF ;
VANDENBERGHE, G .
EUROPEAN JOURNAL OF PEDIATRICS, 1988, 148 (02) :126-131
[8]  
JAEKEN J, 1984, LANCET, V2, P1058
[9]   Adenylosuccinase deficiency presenting with epilepsy in early infancy [J].
MaaswinkelMooij, PD ;
Laan, LAEM ;
Onkenhout, W ;
Brouwer, OF ;
Jaeken, J ;
Poorthuis, BJHM .
JOURNAL OF INHERITED METABOLIC DISEASE, 1997, 20 (04) :606-607
[10]   ADENYLOSUCCINASE DEFICIENCY - A PATIENT WITH IMPAIRED ERYTHROCYTE ACTIVITY AND ANOMALOUS RESPONSE TO INTRAVENOUS FRUCTOSE [J].
SALERNO, C ;
CRIFO, C ;
GIARDINI, O .
JOURNAL OF INHERITED METABOLIC DISEASE, 1995, 18 (05) :602-608