ACUTE INTERMITTENT PORPHYRIA AND EPILEPSY

被引：14

作者：

BIAGINI, R ^{[1
]}

TIGNANI, R ^{[1
]}

FIFI, AR ^{[1
]}

NAPPINI, L ^{[1
]}

机构：

[1] ENTE OSPEDALIERO AREZZO,DIV PEDIAT,AREZZO,ITALY

来源：

ARCHIVES OF DISEASE IN CHILDHOOD | 1979年 / 54卷 / 08期

关键词：

D O I：

10.1136/adc.54.8.644

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

A 14-year-old boy had suffered from intermittent acute hepatic porphyria, myoclonic convulsions, and mental retardation (Lennox- Gastaut syndrome). The porphyria was treated by stopping the administration of phenobarbitone and phenytoin. Sodium valproate at a dose of 70 mg/kg per day lessened the severity and frequency of convulsive crises.

引用

页码：644 / 645

页数：2

共 5 条

[1] ACUTE INTERMITTENT PORPHYRIA IN CHILDHOOD - NEGLECTED DIAGNOSIS
BARCLAY, N
[J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1974, 49 (05) : 404 - 406
[2] ACUTE INTERMITTENT PORPHYRIA WITH SEIZURES
BIRCHFIELD, RI
COWGER, ML
[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1966, 112 (06): : 561 - +
[3] SPECTROPHOTOMETRIC DETERMINATION OF UROPORPHYRINOGEN I SYNTHETASE-ACTIVITY
GRANDCHAMP, B
PHUNG, N
GRELIER, M
NORDMANN, Y
[J]. CLINICA CHIMICA ACTA, 1976, 70 (01) : 113 - 118
[4] HEREDITARY COPROPORPHRIA - STUDY OF A SWEDISH FAMILY
HAEGERARONSEN, B
STATHERS, G
SWAHN, G
[J]. ANNALS OF INTERNAL MEDICINE, 1968, 69 (02) : 221 - +
[5] HEREDITARY COPROPORPHYRIA AND EPILEPSY
HOUSTON, AB
BRODIE, MJ
MOORE, MR
THOMPSON, GG
STEPHENSON, JBP
[J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1977, 52 (08) : 646 - 650

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