SELECTIVE HYPOALDOSTERONISM IN INFANCY - REPORT OF A CASE

被引：3

作者：

CURTIS, JA

MONAGHAN, HP

NEW, MI

BAILEY, JD

机构：

[1] HOSP SICK CHILDREN, DEPT PEDIAT, DIV ENDOCRINOL, TORONTO M5G 1X8, ONTARIO, CANADA

[2] CORNELL UNIV, MED CTR, COLL MED, DEPT PEDIAT, NEW YORK, NY 10021 USA

来源：

AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1983年 / 137卷 / 07期

关键词：

D O I：

10.1001/archpedi.1983.02140330017005

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：633 / 636

页数：4

共 23 条

[1]

BECK JC, 1962, HUMAN ADRENAL CORTEX, P432

[2] ADRENOGENITAL SYNDROME [J].

BONGIOVANNI, AM ;

ROOT, AW .

NEW ENGLAND JOURNAL OF MEDICINE, 1963, 268 (23) :1283-&

[3] A SALT WASTING SYNDROME IN INFANCY [J].

CHEEK, DB ;

PERRY, JW .

ARCHIVES OF DISEASE IN CHILDHOOD, 1958, 33 (169) :252-256

[4]

COHEN T, 1977, CLIN GENET, V11, P25

[5]

DAVID R, 1968, PEDIATRICS, V41, P403

[6] DISTURBANCE OF CORTISOL PRODUCTION IN CONGENITAL ALDOSTERONE DEFICIENCY [J].

DAVID, RR ;

ASNIS, M ;

DRUCKER, WD .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1972, 35 (04) :604-+

[7]

DEGENHART HJ, 1966, ACTA PHYSIOL PHARM N, V14, P88

[8] HYPOALDOSTERONISM IN 3 SIBS DUE TO 18-DEHYDROGENASE DEFICIENCY [J].

HAMILTON, W ;

MCCANDLESS, AE ;

IRELAND, JT ;

GRAY, CE .

ARCHIVES OF DISEASE IN CHILDHOOD, 1976, 51 (08) :576-583

[9]

JEAN R, 1969, ARCH FR PEDIATR, V26, P769

[10] GENETIC-MAPPING OF 21-HYDROXYLASE-DEFICIENCY GENE WITHIN HLA LINKAGE GROUP [J].

LEVINE, LS ;

ZACHMANN, M ;

NEW, MI ;

PRADER, A ;

POLLACK, MS ;

ONEILL, GJ ;

YANG, SY ;

OBERFIELD, SE ;

DUPONT, B .

NEW ENGLAND JOURNAL OF MEDICINE, 1978, 299 (17) :911-915

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