Nonclassic 21-hydroxylase deficiency

被引：7
|
作者：
New, Maria I. [1 ]
机构：
[1] Mt Sinai Sch Med, Dept Pediat, New York, NY 10029 USA
来源：
FERTILITY AND STERILITY | 2006年 / 86卷
关键词：
21-hydroxylase deficiency; congenital adrenal hyperplasia; autosomal recessive disorders;
D O I：
10.1016/j.fertnstert.2006.03.005
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
Nonclassic 21-hydroxylase deficiency is a frequent autosomal recessive disorder which causes decreased fertility and is easily treated. It occurs with the highest frequency of any-other autosomal recessive disorder in humans (Fertl Steril (R) 2006;86(Suppl 1);S2. (c) 2006 by American Society for Reproductive Medicine.).
引用
收藏
页码：S2 / S2
页数：1
相关论文
共 50 条
  • [1] Nonclassic 21-hydroxylase deficiency
    Dewailly, D
    [J]. SEMINARS IN REPRODUCTIVE MEDICINE, 2002, 20 (03) : 243 - 248
  • [2] Nonclassic 21-hydroxylase deficiency in Croatia
    Dumic, M
    Ille, J
    Zunec, R
    Plavsic, V
    Francetic, I
    Skrabic, V
    Janjanin, N
    Spehar, A
    Wei, JQ
    Wilson, RC
    New, MI
    [J]. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2004, 17 (02): : 157 - 164
  • [3] Fertility and pregnancy outcomes in women with nonclassic 21-hydroxylase deficiency
    Carriere, Camille
    Nguyen, Lee S.
    Courtillot, Carine
    Tejedor, Isabelle
    Chakhtoura, Zeina
    Bellanne-Chantelot, Christine
    Tardy, Veronique
    Leban, Monique
    Touraine, Philippe
    Bachelot, Anne
    [J]. CLINICAL ENDOCRINOLOGY, 2023, 98 (03) : 315 - 322
  • [4] NONCLASSIC ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
    DRUCKER, S
    NEW, MI
    [J]. PEDIATRIC CLINICS OF NORTH AMERICA, 1987, 34 (04) : 1067 - 1081
  • [5] CLINICAL AND GENETIC-CHARACTERIZATION OF NONCLASSIC 21-HYDROXYLASE DEFICIENCY
    SPEISER, PW
    NEW, MI
    WHITE, PC
    [J]. ENDOCRINE RESEARCH, 1989, 15 (1-2) : 257 - 276
  • [6] AN UPDATE ON THE FREQUENCY OF NONCLASSIC DEFICIENCY OF ADRENAL 21-HYDROXYLASE IN THE YUGOSLAV POPULATION
    DUMIC, M
    BRKLJACIC, L
    SPEISER, PW
    WOOD, E
    CRAWFORD, C
    PLAVSIC, V
    BANICEVIAC, M
    RADMANOVIC, S
    RADICA, A
    KASTELAN, A
    NEW, MI
    [J]. ACTA ENDOCRINOLOGICA, 1990, 122 (06): : 703 - 710
  • [7] Cushing Disease and Cryptic 21-Hydroxylase Deficiency in the Mother of Two Daughters with Nonclassic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
    Flint, A. C.
    Merke, D. P.
    Nieman, L. K.
    Witchel, S. F.
    [J]. ENDOCRINE REVIEWS, 2010, 31 (03)
  • [8] Nonclassic 21-Hydroxylase Deficiency and Short Stature in an Ethnically at-Risk Population
    Agarwal, Chhavi
    Hassoun, Abeer
    Aranoff, Gaya
    Pomeranz, Christy
    Oberfield, Sharon E.
    [J]. ENDOCRINOLOGIST, 2010, 20 (04): : 194 - 197
  • [9] 21-hydroxylase deficiency
    Newfield, RS
    New, MI
    [J]. ADOLESCENT GYNECOLOGY AND ENDOCRINOLOGY: BASIC AND CLINICAL ASPECTS, 1997, 816 : 219 - 229
  • [10] Nonclassic Adrenal Hyperplasia (NCAH) due to 21-hydroxylase deficiency: A cohort of 78 patients
    Wan, Zhihan
    Wang, Wencui
    Zheng, Sichang
    Han, Rulai
    Xie, Xiaoyan
    Zhao, Yu
    Wang, Weiqing
    Sun, Shouyue
    Ye, Lei
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2023, 225
12345