FAMILIAL OCCURENCE OF FORMIMINOTRANSFERASE DEFICIENCY SYNDROME

被引：14

作者：

ARAKAWA, T

TAMURA, T

OHARA, K

NARISAWA, K

TANNO, K

HONDA, Y

HIGASHI, O

机构：

[1] Department of Pediatrics, Faculty of Medicine, Tohoku University, Sendai

来源：

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE | 1968年 / 96卷 / 03期

关键词：

D O I：

10.1620/tjem.96.211

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Clinical and biochemical findings of two siblings with formiminotransferase deficiency syndrome in a family were described and a hereditary background of this disorder was suggested. © 1968, Tohoku University Medical Press. All rights reserved.

引用

页码：211 / 217

页数：7

共 6 条

[1] HYPERFOLIC-ACIDEMIA WITH FORMIMINOGLUTAMIC-ACIDURIA FOLLOWING HISTIDINE LOADING - SUGGESTED FOR A CASE OF CONGENITAL DEFICIENCY IN FORMIMINOTRANSFERASE [J].

ARAKAWA, T ;

KUDO, Z ;

TADA, K ;

MIZUNO, T ;

HAYASHI, T ;

OHARA, K .

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 1963, 80 (04) :370-382

[2] FORMIMINOTRANSFERASE DEFICIENCY SYNDROME ASSOCIATED WITH MEGALOBLASTIC ANEMIA RESPONSIVE TO PYRIDOXINE OR FOLIC ACID [J].

ARAKAWA, T ;

TAMURA, T ;

HIGASHI, O ;

OHARA, K ;

TANNO, K ;

HONDA, Y ;

NARISAWA, K ;

KONNO, T ;

WADA, Y ;

SATO, Y ;

MIZUNO, T .

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 1968, 94 (01) :3-16

[3]

ARAKAWA T, 1965, ANN PAEDIAT, V250, P1

[4]

LUHBY AL, 1959, P SOC EXP BIOL MED, V101, P350, DOI 10.3181/00379727-101-24936

[5]

MACDONALD RA, 1965, ARCH PATHOL, V80, P153

[6] TETRAHYDROFOLATE-DEPENDENT ENZYME ACTIVITIES OF RAT LIVER IN RIBOFLAVIN DEFICIENCY [J].

NARISAWA, K ;

TAMURA, T ;

TANNO, K ;

OHARA, K ;

ARAKAWA, T .

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 1968, 94 (04) :417-430

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