Miscarriages in Families with a Child with Classic Congenital Adrenal Hyperplasia and 21-Hydroxylase Deficiency (CAH)

被引：0
|
作者：
Penger, Theresa [1 ]
Hess, Johannes [1 ]
Marx, Michaela [1 ]
Oppelt, Patricia [2 ]
Doerr, Helmuth-Guenther [1 ]
机构：
[1] Univ Hosp Erlangen, Dept Pediat, Pediat Endocrinol, Erlangen, Germany
[2] Univ Hosp, Dept Gynecol & Obstet, Pediat Gynecol, Erlangen, Germany
来源：
HORMONE RESEARCH IN PAEDIATRICS | 2018年 / 90卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P2-P007
引用
收藏
页码：140 / 140
页数：1
相关论文
共 50 条
  • [1] Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
    Doerr, Helmuth G.
    Hess, Johannes
    Penger, Theresa
    Marx, Michaela
    Oppelt, Patricia
    [J]. BMC PREGNANCY AND CHILDBIRTH, 2018, 18
  • [2] Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
    Helmuth G. Dörr
    Johannes Hess
    Theresa Penger
    Michaela Marx
    Patricia Oppelt
    [J]. BMC Pregnancy and Childbirth, 18
  • [3] Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
    Helmuth G. Dörr
    Hartmut A. Wollmann
    Berthold P. Hauffa
    Joachim Woelfle
    [J]. BMC Endocrine Disorders, 18
  • [4] Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
    Doerr, Helmuth G.
    Wollmann, Hartmut A.
    Hauffa, Berthold P.
    Woelfle, Joachim
    [J]. BMC ENDOCRINE DISORDERS, 2018, 18
  • [5] Therapy of classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency in childhood and youth
    Bonfig, Walter
    Kapelari, Klaus
    Riedl, Stefan
    [J]. AUSTRIAN JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM, 2019, 12 (04): : 137 - 140
  • [6] CLINICAL AND MOLECULAR STUDIES OF 21 BRAZILIAN FAMILIES WITH CLASSIC CONGENITAL ADRENAL-HYPERPLASIA (CAH) DUE TO 21-HYDROXYLASE DEFICIENCY
    GUERRA, G
    MELLO, MP
    FARAH, SB
    ARAUJO, M
    BAPTISTA, MTM
    MARINI, SHVL
    [J]. PEDIATRIC RESEARCH, 1995, 38 (04) : 20 - 20
  • [7] Adiponectin levels are high in children with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency
    Voelkl, Thomas M. K.
    Simm, Diemud
    Koerner, Antje
    Kiess, Wieland
    Kratzsch, Juergen
    Doerr, Helmuth G.
    [J]. ACTA PAEDIATRICA, 2009, 98 (05) : 885 - 891
  • [8] LATE ONSET 21-HYDROXYLASE DEFICIENCY IS A GENETIC VARIANT OF THE CLASSIC FORM OF CONGENITAL ADRENAL-HYPERPLASIA (CAH)
    CHROUSOS, GP
    CUTLER, GB
    MANN, D
    LORIAUX, DL
    [J]. PEDIATRIC RESEARCH, 1981, 15 (12) : 1556 - 1556
  • [9] Altered leptin axis in children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH)
    Voelkl, Thomas M. K.
    Simm, Diemud
    Koerner, Antje
    Kiess, Wieland
    Kratzsch, Juergen
    Doerr, Helmuth G.
    [J]. HORMONE RESEARCH, 2006, 65 : 88 - 88
  • [10] 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
    Shaw, Amy M.
    [J]. NEONATAL NETWORK, 2010, 29 (03): : 191 - 196
12345