Premature ovarian failure

被引:190
作者
Kalantaridou, SN
Davis, SR
Nelson, LM
机构
[1] NICHHD, Sect Womens Hlth, DEB, NIH, Bethesda, MD 20892 USA
[2] Jean Hailes Fdn Res Unit, Melbourne, Vic, Australia
关键词
D O I
10.1016/S0889-8529(05)70051-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Premature ovarian failure is a condition causing amenorrhea, infertility, sex steroid deficiency, and elevated gonadotropins in women 40 years old or younger. Premature ovarian failure is not merely an early natural menopause. Young women with premature ovarian failure may ovulate intermittently and, indeed, pregnancies have occurred after the diagnosis of ovarian failure. Premature ovarian failure may be associated with other autoimmune disorders, such as autoimmune adrenal failure, hypothyroidism,diabetes mellitus. Premature ovarian failure has both significant psychosocial sequelae and major health implications. Young women with this disorder need a thorough assessment, sex steroid replacement, and long-term surveillance to monitor their therapy and minimize their health risks in later life.
引用
收藏
页码:989 / +
页数:20
相关论文
共 126 条
[1]   An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains [J].
Aaltonen, J ;
Bjorses, P ;
Perheentupa, J ;
HorelliKuitunen, N ;
Palotie, A ;
Peltonen, L ;
Lee, YS ;
Francis, F ;
Hennig, S ;
Thiel, C ;
Lehrach, H ;
Yaspo, ML .
NATURE GENETICS, 1997, 17 (04) :399-403
[2]   CLINICAL VARIATION OF AUTOIMMUNE POLYENDOCRINOPATHY CANDIDIASIS ECTODERMAL DYSTROPHY (APECED) IN A SERIES OF 68 PATIENTS [J].
AHONEN, P ;
MYLLARNIEMI, S ;
SIPILA, I ;
PERHEENTUPA, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (26) :1829-1836
[3]   THE EXPRESSION OF AUTOIMMUNE POLYGLANDULAR DISEASE TYPE-I APPEARS ASSOCIATED WITH SEVERAL HLA-A ANTIGENS BUT NOT WITH HLA-DR [J].
AHONEN, P ;
KOSKIMIES, S ;
LOKKI, ML ;
TIILIKAINEN, A ;
PERHEENTUPA, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 66 (06) :1152-1157
[4]  
AIMAN J, 1985, OBSTET GYNECOL, V66, P9
[5]   Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene [J].
Aittomaki, K ;
Herva, R ;
Stenman, UH ;
Juntunen, K ;
Ylostalo, P ;
Hovatta, O ;
delaChapelle, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (10) :3722-3726
[6]   MUTATION IN THE FOLLICLE-STIMULATING-HORMONE RECEPTOR GENE CAUSES HEREDITARY HYPERGONADOTROPIC OVARIAN FAILURE [J].
AITTOMAKI, K ;
LUCENA, JLD ;
PAKARINEN, P ;
SISTONEN, P ;
TAPANAINEN, J ;
GROMOLL, J ;
KASKIKARI, R ;
SANKILA, EM ;
LEHVASLAIHO, H ;
ENGEL, AR ;
NIESCHLAG, E ;
HUHTANIEMI, I ;
DELACHAPELLE, A .
CELL, 1995, 82 (06) :959-968
[7]  
ALPER MA, 1986, OBSTET GYNECOL, V67, P59
[8]   KARYOTYPICALLY NORMAL SPONTANEOUS PREMATURE OVARIAN FAILURE - EVALUATION OF ASSOCIATION WITH THE CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX [J].
ANASTI, JN ;
ADAMS, S ;
KIMZEY, LM ;
DEFENSOR, RA ;
ZACHARY, AA ;
NELSON, LM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (03) :722-723
[9]   Bone loss in young women with karyotypically normal spontaneous premature ovarian failure [J].
Anasti, JN ;
Kalantaridou, SN ;
Kimzey, LM ;
Defensor, RA ;
Nelson, LM .
OBSTETRICS AND GYNECOLOGY, 1998, 91 (01) :12-15
[10]  
ANASTI JN, 1994, FERTIL STERIL, V62, P726