MACROCEPHALY, DYSTONIA, AND BILATERAL TEMPORAL ARACHNOID CYSTS - GLUTARIC ACIDURIA TYPE-1

被引:37
作者
MARTINEZLAGE, JF
CASAS, C
FERNANDEZ, MA
PUCHE, A
COSTA, TR
POZA, M
机构
[1] UNIV HOSP VIRGEN ARRIXACA,NEUROPEDIAT SECT,E-30120 MURCIA,SPAIN
[2] AUTONOMOUS COMMUNITY,CTR CLIN BIOCHEM & GENET,ESPINARDO,SPAIN
关键词
BILATERAL ARACHNOID CYSTS; DYSTONIA; GLUTARIC ACIDURIA TYPE 1; HYDROCEPHALUS; MACROCEPHALY; ORGANIC ACIDURIAS;
D O I
10.1007/BF00301092
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Two siblings presented with macrocephaly, psychomotor delay, and progressive dystonia. The initial diagnosis was of hydrocephalus and bilateral temporal cerebrospinal fluid collections. Following ventriculoperitoneal shunting, the patients showed only modest neurological improvement. Metabolic investigations performed later in the course of the disease disclosed increased levels of glutaric acid in the urine and decreased levels of serum carnitine, which were confirmatory of glutaric aciduria type 1. The association of macrocephaly, dystonia, and bilateral temporal arachnoid cysts, shown either by computed tomography or magnetic resonance imaging, seems to be diagnostic of glutaric aciduria type 1. The authors report these two cases as they think they might be of interest to neurosurgeons.
引用
收藏
页码:198 / 203
页数:6
相关论文
共 22 条
[1]  
ALTMAN NR, 1991, AM J NEURORADIOL, V12, P966
[2]   GLUTARIC ACIDURIA TYPE-1 - ENZYMATIC AND NEURORADIOLOGIC INVESTIGATIONS OF 2 KINDREDS [J].
AMIR, N ;
ELPELEG, ON ;
SHALEV, RS ;
CHRISTENSEN, E .
JOURNAL OF PEDIATRICS, 1989, 114 (06) :983-989
[3]   GLUTARIC ACIDURIA TYPE-I - CLINICAL HETEROGENEITY AND NEURORADIOLOGICAL FEATURES [J].
AMIR, N ;
ELPELEG, O ;
SHALEV, RS ;
CHRISTENSEN, E .
NEUROLOGY, 1987, 37 (10) :1654-1657
[4]   GLUTARIC ACIDURIA TYPE-1 - BIOCHEMICAL INVESTIGATIONS AND POSTMORTEM FINDINGS [J].
BENNETT, MJ ;
MARLOW, N ;
POLLITT, RJ ;
WALES, JKH .
EUROPEAN JOURNAL OF PEDIATRICS, 1986, 145 (05) :403-405
[5]  
BERGMAN I, 1989, PEDIATRICS, V83, P228
[6]   GLUTARIC ACIDURIA TYPE-I - PRENATAL EXCLUSION USING GC-MS ANALYSIS OF AMNIOTIC-FLUID AND ENZYMOLOGY WITH OXIDATION OF [6-C-14]LYSINE [J].
CHALMERS, RA ;
CHENG, KN ;
ENGLISH, NR ;
JONES, MA ;
SAVAGE, W .
JOURNAL OF INHERITED METABOLIC DISEASE, 1989, 12 (03) :335-336
[7]  
CHRISTENSEN E, 1989, J INHERITED METAB S2, V12, P227
[8]   VIGABATRIN IN THE TREATMENT OF GLUTARIC ACIDURIA TYPE-I [J].
FRANCOIS, B ;
JAEKEN, J ;
GILLIS, P .
JOURNAL OF INHERITED METABOLIC DISEASE, 1990, 13 (03) :352-354
[9]   GLUTARIC ACIDURIA - NEW DISORDER OF AMINO-ACID METABOLISM [J].
GOODMAN, SI ;
MARKEY, SP ;
MOE, PG ;
MILES, BS ;
TENG, CC .
BIOCHEMICAL MEDICINE, 1975, 12 (01) :12-21
[10]  
GOODMAN SI, 1977, J PEDIATR-US, V90, P746, DOI 10.1016/S0022-3476(77)81240-7