Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiency

被引:23
作者
Baethmann, M
Wendel, U
Hoffmann, GF
Göhlich-Ratmann, G
Kleinlein, B
Seiffert, P
Blom, H
Voit, T
机构
[1] Univ Hosp, Dept Pediat, D-45122 Essen, Germany
[2] Univ Hosp, Dept Pediat, Dusseldorf, Germany
[3] Univ Heidelberg Hosp, Dept Pediat 1, Heidelberg, Germany
[4] St Johannes Hosp, Duisburg, Germany
[5] Univ Nijmegen Hosp, Dept Pediat, NL-6500 HB Nijmegen, Netherlands
关键词
hydrocephalus internus in metabolic disorders single carbon metabolism; homocysteine; methylenetetrahydrofolate;
D O I
10.1055/s-2000-12947
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Hydrocephalus internus (HCl) of all four ventricles in association with early neurological abnormalities is described as the presenting symptom in two patients with 5,10-methylenetetrahydrofolate reductase (MTHFR) deficiency. Decreased activity of MTHFR leads to reduction of 5-methyltetrahydrofolate, the main methyl donor for methionine synthesis necessary for synthesis of S-adenosyl-methionine (SAM). Demyelination in MTHFR deficiency has been attributed to low SAM levels in the brain. The biochemical hallmarks of the disorder are hyperhomocystinemia, homocystinuria and low levels of plasma methionine. Hydrocephalus internus requiring neurosurgical intervention has to our knowledge not been reported as a presenting feature of homocystinuria due to deficiency of MTHFR so Far. The surprising finding of HCl of all four ventricles in MTHFR deficiency must be kept in mind when evaluating patients with hydrocephalus of unknown origin.
引用
收藏
页码:314 / 317
页数:4
相关论文
共 19 条
[1]   COMPUTED-TOMOGRAPHY AND MAGNETIC-RESONANCE-IMAGING OF THE BRAIN IN HURLERS DISEASE [J].
AFIFI, AK ;
SATO, Y ;
WAZIRI, MH ;
BELL, WE .
JOURNAL OF CHILD NEUROLOGY, 1990, 5 (03) :235-241
[2]  
ALLEN RJ, 1980, ANN NEUROL, V8, P211
[3]   CERVICAL CORD COMPRESSION AND SEVERE HYDROCEPHALUS IN A CHILD WITH SAUDI VARIANT OF MULTIPLE SULFATASE DEFICIENCY - REPORT OF CASE [J].
ALMOUTAERY, KR ;
CHOUDHURY, AR ;
HASSANEN, MO .
ACTA NEUROCHIRURGICA, 1994, 131 (1-2) :160-163
[4]  
BECK M, 1991, MONATSSCHR KINDERH, V139, P120
[5]   EARLY MANIFESTATIONS OF MULTIPLE SULFATASE DEFICIENCY [J].
BURK, RD ;
VALLE, D ;
THOMAS, GH ;
MILLER, C ;
MOSER, A ;
MOSER, H ;
ROSENBAUM, KN .
JOURNAL OF PEDIATRICS, 1984, 104 (04) :574-578
[6]  
ENGBERSEN AMT, 1995, AM J HUM GENET, V56, P142
[7]  
Engelbrecht V, 1997, AM J NEURORADIOL, V18, P536
[8]   FOLATE-RESPONSIVE HOMOCYSTINURIA AND SCHIZOPHRENIA - DEFECT IN METHYLATION DUE TO DEFICIENT 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE-ACTIVITY [J].
FREEMAN, JM ;
FINKELSTEIN, JD ;
MUDD, SH .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (10) :491-496
[9]  
GOYETTE P, 1995, AM J HUM GENET, V56, P1052
[10]   HOMOCYSTINURIA CAUSED BY 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY - A CASE IN AN INFANT RESPONDING TO METHIONINE, FOLINIC ACID, PYRIDOXINE, AND VITAMIN-B12 THERAPY [J].
HARPEY, JP ;
ROSENBLATT, DS ;
COOPER, BA ;
LEMOEL, G ;
ROY, C ;
LAFOURCADE, J .
JOURNAL OF PEDIATRICS, 1981, 98 (02) :275-278