Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline (vol 95, pg 4133, 2010)

被引：2
|
作者：
Speiser, P. W.
Azziz, R.
Baskin, L. S.
Ghizzoni, L.
Hensle, T. W.
Merke, D. P.
Meyer-Bahlburg, H. F. L.
Miller, W. L.
Montori, V. M.
Oberfield, S. E.
Ritzen, M.
White, P. C.
机构：
来源：
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2021年 / 106卷 / 07期
关键词：
D O I：
10.1210/clinem/dgab316
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：E2853 / E2853
页数：1
相关论文
共 50 条
  • [31] Congenital adrenal hyperplasia due to 21-hydroxylase deficiency - management in adults
    Ambroziak, Urszula
    Bednarczuk, Tomasz
    Ginalska-Malinowska, Maria
    Malunowicz, Ewa Maria
    Grzechocinska, Barbara
    Kaminski, Pawel
    Bablok, Leszek
    Przedlacki, Jerzy
    Bar-Andziak, Ewa
    ENDOKRYNOLOGIA POLSKA, 2010, 61 (01) : 142 - 155
  • [32] GUIDELINES FOR TREATMENT OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
    Dumic, Miroslav
    PAEDIATRIA CROATICA, 2012, 56 : 31 - 32
  • [33] Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia
    Doleschall Marton
    Torok Dora
    Meszaros Katalin
    Luczay Andrea
    Halasz Zita
    Nemeth Krisztina
    Suzcs Nikolette
    Kiss Robert
    Toke Judit
    Solyom Janos
    Fekete Gyorgy
    Patocs Attila
    Igaz Peter
    Toth Miklos
    ORVOSI HETILAP, 2018, 159 (07) : 269 - 277
  • [34] Prenatal diagnosis and treatment of steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)
    Roli Mathur
    Madhulika Kabra
    The Indian Journal of Pediatrics, 2000, 67 (11) : 813 - 818
  • [35] 21-HYDROXYLASE DEFICIENCY CONGENITAL ADRENAL-HYPERPLASIA
    NEW, MI
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1994, 48 (01): : 15 - 22
  • [36] Molecular characterization of mutations in Indian children with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
    Mathur, R
    Menon, PSN
    Kabra, M
    Goyal, RK
    Verma, IC
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2001, 14 (01): : 27 - 35
  • [37] Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
    Speiser, PW
    ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 2001, 30 (01) : 31 - +
  • [38] Mutational characterization of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Malaysia
    Balraj, P.
    Lim, P. G.
    Sidek, H.
    Wu, L. L.
    Khoo, A. S. B.
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2013, 36 (06) : 366 - 374
  • [39] Congenital adrenal hyperplasia due to 21-hydroxylase deficiency associated with bilateral keratoconus
    Incorvaia, C
    Parmeggiani, F
    Costagliola, C
    Perri, P
    Tittoni, M
    Sebastiani, A
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 2003, 135 (04) : 557 - 559
  • [40] Barriers to the Management of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
    Eitel, Kelsey B.
    Fechner, Patricia Y.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2025, 110 : S67 - S73
12345