PROPIONIC ACIDEMIA AND HYPERLYSINEMIA IN A CASE WITH ORNITHINE TRANSCARBAMYLASE (OTC) DEFICIENCY

被引：12

作者：

KRIEGER, I

BACHMANN, C

GRONEMEYER, WH

CEJKA, J

机构：

[1] WAYNE STATE UNIV, CHILDRENS HOSP, SCH MED, DEPT PEDIAT, DETROIT, MI 48201 USA

[2] UNIV CALIF SAN DIEGO, DEPT PEDIAT, LA JOLLA, CA 92037 USA

来源：

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 1976年 / 43卷 / 04期

关键词：

D O I：

10.1210/jcem-43-4-796

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：796 / 802

页数：7

共 27 条

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[2]

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[3]

BACHMANN C, 1974, HERITABLE DISORDERS, P374

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FABRE, LF .

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[5]

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[7] FAMILIAL HYPERLYSINEMIA WITH LYSINE-KETOGLUTARATE REDUCTASE INSUFFICIENCY [J].

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HUTZLER, J ;

COX, RP ;

WOODY, NC .

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[8]

DANCIS J, 1974, HERITABLE DISORDERS, P387

[9]

FORMAN DT, 1964, CLIN CHEM, V10, P497

[10] CONGENITAL HYPERAMMONEMIA - ASSOCIATION WITH HYPERGLYCINEMIA AND DECREASED LEVELS OF CARBAMYL PHOSPHATE SYNTHETASE [J].

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CARTER, S .

ARCHIVES OF NEUROLOGY, 1970, 23 (05) :430-+

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