Early hypertension and prolonged mineralocorticoid therapy discontinuation in a child with salt-wasting 21-hydroxylase deficiency

被引：1
|
作者：
Wasniewska, M. [1 ]
Valenzise, M. [1 ]
Aversa, T. [1 ]
Mirabelli, S. [1 ]
De Luca, F. [1 ]
De Luca, F. L. [1 ]
Lombardo, F. [1 ]
机构：
[1] Univ Messina, Dept Pediat, Messina, Italy
来源：
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | 2011年 / 34卷 / 02期
关键词：
CONGENITAL ADRENAL-HYPERPLASIA; BLOOD-PRESSURE; DEVELOPMENTAL EXPRESSION; ADOLESCENTS; CYP2C19;
D O I：
10.1007/BF03347048
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：159 / 161
页数：3
相关论文
共 50 条
  • [21] ALDOSTERONE SYNTHESIS IN SALT-WASTING CONGENITAL ADRENAL-HYPERPLASIA WITH COMPLETE ABSENCE OF ADRENAL 21-HYDROXYLASE
    SPEISER, PW
    AGDERE, L
    UESHIBA, H
    WHITE, PC
    NEW, MI
    NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (03): : 145 - 149
  • [22] PRESENTATION, ACUTE ILLNESS, AND LEARNING-DIFFICULTIES IN SALT WASTING 21-HYDROXYLASE DEFICIENCY
    DONALDSON, MDC
    THOMAS, PH
    LOVE, JG
    MURRAY, GD
    MCNINCH, AW
    SAVAGE, DCL
    ARCHIVES OF DISEASE IN CHILDHOOD, 1994, 70 (03) : 214 - 218
  • [23] Timing of hyponatremia development in patients with salt-wasting-type 21-hydroxylase deficiency
    Shima, Rohi
    Sawano, Kentaro
    Shibata, Nao
    Nyuzuki, Hiromi
    Sasaki, Sunao
    Sato, Hidetoshi
    Ogawa, Yohei
    Abe, Yuki
    Nagasaki, Keisuke
    Saitoh, Akihiko
    CLINICAL PEDIATRIC ENDOCRINOLOGY, 2020, 29 (03) : 105 - 110
  • [24] Aldosterone Synthase Deficiency: A Rare Cause of Salt-Wasting Syndrome in a Child
    Barbaria, Wiem
    Bourcheda, Manel
    Karabibene, Eya
    Jendoubi, Jihene
    Khamassi, Ichrak
    INDIAN JOURNAL OF PEDIATRICS, 2024, 91 (12): : 1299 - 1299
  • [25] Failure of cortisone acetate therapy in 21-hydroxylase deficiency in early infancy
    Jinno, K
    Sakura, N
    Nomura, S
    Fujitaka, N
    Ueda, K
    Kihara, M
    PEDIATRICS INTERNATIONAL, 2001, 43 (05) : 478 - 482
  • [26] Interaction between accumulated 21-deoxysteroids and mineralocorticoid signaling in 21-hydroxylase deficiency
    Travers, Simon
    Bouvattier, Claire
    Fagart, Jerome
    Martinerie, Laetitia
    Viengchareun, Say
    Pussard, Eric
    Lombes, Marc
    AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2020, 318 (02): : E102 - E110
  • [27] Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndrome
    Parker, Elizabeth A.
    Hovanes, Karine
    Germak, John
    Porter, Forbes
    Merke, Deborah P.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (20) : 2236 - 2240
  • [28] Observation of hypertension in children with 21-hydroxylase deficiency - A preliminary report
    Nebesio, Todd D.
    Eugster, Erica A.
    ENDOCRINE, 2006, 30 (03) : 279 - 282
  • [29] EXTENDED MHC HAPLOTYPES IN SALT-LOSING 21-HYDROXYLASE DEFICIENCY
    ALPER, CA
    FLEISCHNICK, E
    AWDEH, Z
    RAUM, D
    CRIGLER, JF
    GERALD, PS
    YUNIS, EJ
    ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1985, 458 : 28 - 35
  • [30] SALT-WASTING CONGENITAL ADRENAL-HYPERPLASIA - DETECTION AND CHARACTERIZATION OF MUTATIONS IN THE STEROID 21-HYDROXYLASE GENE, CYP21, USING THE POLYMERASE CHAIN-REACTION
    OWERBACH, D
    BALLARD, AL
    DRAZNIN, MB
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 74 (03): : 553 - 558
12345