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 50 条
  • [1] PRENATAL-DIAGNOSIS OF 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY
    CHRISTENSEN, E
    BRANDT, NJ
    NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (01): : 50 - 51
  • [2] INFANTILE TYPE OF HOMOCYSTINURIA WITH 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY
    WADA, Y
    NARISAWA, K
    ARAKAWA, T
    HUMAN HEREDITY, 1977, 27 (03) : 219 - 219
  • [3] Nitrous oxide and 5,10-methylenetetrahydrofolate reductase deficiency.
    Selzer, RR
    Rosenblatt, DS
    Laxova, R
    Hogan, K
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 429 - 429
  • [4] 5,10-Methylenetetrahydrofolate reductase deficiency with progressive polyneuropathy in an infant
    Tsuji, Megumi
    Takagi, Atsushi
    Sameshima, Kiyoko
    Iai, Mizue
    Yamashita, Sumimasa
    Shinbo, Hiroko
    Furuya, Noritaka
    Kurosawa, Kenji
    Osaka, Hitoshi
    BRAIN & DEVELOPMENT, 2011, 33 (06): : 521 - 524
  • [5] A CASE OF INFANTILE FORM OF 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY
    HARPEY, JP
    LEMOEL, G
    TROUPEL, S
    ROSENBLATT, DS
    COOPER, BA
    JOURNAL OF CLINICAL CHEMISTRY AND CLINICAL BIOCHEMISTRY, 1981, 19 (08): : 692 - 692
  • [6] FOLLOW-UP IN A CHILD WITH 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY
    HARPEY, JP
    LEMOEL, G
    ZITTOUN, J
    JOURNAL OF PEDIATRICS, 1983, 103 (06): : 1007 - 1007
  • [7] CASE OF HOMOCYSTINURIA DUE TO 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY IN AN INFANT
    HARPEY, JP
    ROSENBLATT, DS
    COOPER, BA
    ROY, C
    LAFOURCADE, J
    LEMOEL, G
    ARCHIVES FRANCAISES DE PEDIATRIE, 1980, 37 : 62 - 63
  • [8] BETAINE IN THE TREATMENT OF HOMOCYSTINURIA DUE TO 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY
    WENDEL, U
    BREMER, HJ
    EUROPEAN JOURNAL OF PEDIATRICS, 1984, 142 (02) : 147 - 150
  • [9] AN AUTOPSY CASE OF HOMOCYSTINURIA DUE TO 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY
    NISHIMURA, M
    TOMITA, Y
    TAKASHIMA, S
    TANAKA, J
    YOSHINO, K
    NARISAWA, K
    KUROBANE, I
    BRAIN & DEVELOPMENT, 1986, 8 (02): : 208 - 208
  • [10] Nitrous oxide and 5,10-methylenetetrahydrofolate reductase
    Kaufman, JL
    NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (15): : 1479 - 1479