MALIGNANT HYPERTENSION IN CONGENITAL ADRENAL-HYPERPLASIA DUE TO 11-BETA-HYDROXYLASE DEFICIENCY

被引:30
|
作者
HAGUE, WM
HONOUR, JW
机构
[1] NO GEN HOSP,DEPT MED,SHEFFIELD S5 7AU,S YORKSHIRE,ENGLAND
[2] CLIN RES CTR,DIV CLIN CHEM,HARROW HA1 3UJ,MIDDX,ENGLAND
关键词
D O I
10.1111/j.1365-2265.1983.tb02880.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:505 / 510
页数:6
相关论文
共 50 条
  • [41] NEW STUDIES OF THE 11-BETA-HYDROXYLASE AND 18-HYDROXYLASE ENZYMES IN THE HYPERTENSIVE FORM OF CONGENITAL ADRENAL-HYPERPLASIA
    LEVINE, LS
    RAUH, W
    GOTTESDIENER, K
    CHOW, D
    GUNCZLER, P
    RAPAPORT, R
    PANG, S
    SCHNEIDER, B
    NEW, MI
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1980, 50 (02): : 258 - 263
  • [42] CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
    CUTLER, GB
    ROSEN, H
    BLANKSEGAL, M
    MAJZOUB, J
    LAUE, L
    NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (26): : 1806 - 1813
  • [43] Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: description of a new mutation, R384X
    Mary Matallana-Rhoades, Audrey
    David Corredor-Castro, Juan
    Javier Bonilla-Escobar, Francisco
    Valentina Mecias-Cruz, Bony
    Mejia de Beldjena, Liliana
    COLOMBIA MEDICA, 2016, 47 (03): : 172 - 175
  • [44] 11-BETA HYDROXYLASE DEFICIENCY IN CONGENITAL ADRENAL HYPERPLASIA IN THE ABSENCE OF HYPERTENSION
    GANDY, HM
    KEUTMANN, EH
    AMA JOURNAL OF DISEASES OF CHILDREN, 1958, 96 (04): : 519 - 519
  • [45] Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations
    Menabo, Soara
    Polat, Seher
    Baldazzi, Lilia
    Kulle, Alexandra E.
    Holterhus, Paul-Martin
    Groetzinger, Joachim
    Fanelli, Flaminia
    Balsamo, Antonio
    Riepe, Felix G.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2014, 22 (05) : 610 - 616
  • [46] Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations
    Soara Menabò
    Seher Polat
    Lilia Baldazzi
    Alexandra E Kulle
    Paul-Martin Holterhus
    Joachim Grötzinger
    Flaminia Fanelli
    Antonio Balsamo
    Felix G Riepe
    European Journal of Human Genetics, 2014, 22 : 610 - 616
  • [47] CONGENITAL ADRENAL-HYPERPLASIA DUE TO 11 BETA-HYDROXYLASE DEFICIENCY - FINAL DIAGNOSIS IN ADULT AGE IN 3 PATIENTS
    GLENTHOJ, A
    NIELSEN, MD
    STARUP, J
    ACTA ENDOCRINOLOGICA, 1980, 93 (01): : 94 - 99
  • [48] Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: clinical, biochemical and molecular characteristics and long-term outcomes
    Santis, Elida Mercado
    Campos, Ariadna
    Fernandez, Paula
    Oriola, Josep
    Yeste, Diego
    Perez, Victor
    Clemente, Maria
    ANALES DE PEDIATRIA, 2025, 102 (02):
  • [49] ADRENALECTOMY(A) IN UNMANAGEABLE CONGENITAL ADRENAL HYPERPLASIA(CAH) DUE TO 21-BETA-HYDROXYLASE AND 11-BETA-HYDROXYLASE DEFICIENCY(21OHD AND 11-BETA-OHD)
    ZACHMANN, M
    MAUME, BF
    PRADER, A
    PEDIATRIC RESEARCH, 1984, 18 (01) : 103 - 103
  • [50] Over 50 years of progress in the treatment of the hypertensive form of congenital adrenal hyperplasia due to steroid 11-beta-hydroxylase deficiency
    Migeon, Claude J.
    HORMONE RESEARCH, 2007, 68 (06) : 298 - 299