Krone N, Wachter I, Stefanidou M, Roscher A A, Schwarz H P
University Children's Hospital, Munich, Germany.
Clin Endocrinol (Oxf). 2001 Oct;55(4):523-9. doi: 10.1046/j.1365-2265.2001.01359.x.
Fertility rates in women with congenital adrenal hyperplasia (CAH) are reported to be poor, but few data are available. We assessed rates and course of pregnancy, mode of delivery and long-term outcome of offspring from women with CAH.
A large cohort of women with CAH due to 21-hydroxylase deficiency had initially been diagnosed and followed at one centre. Those women who had given birth were contacted. Information was gathered from hospital records, direct patient contact, structured questionnaire and the Documentation of Pregnancy and Preventive Care Booklets.
Between 1978 and 1998, 18 women with CAH (one salt wasting, 12 simple virilizing, five nonclassical) had given birth to 31 children (18 females, 13 males). Delivery was by Caesarean section in 16 out of the 31 children. None of the female newborns was masculinized. Twenty-nine children were born at term, five children were small for gestational age (SGA). Postnatal development was basically normal in all children; 18 are now older than 10 years, seven are between 5 and 10 years old, six are less than 5 years old.
Fertility is reduced in females with CAH, especially those with the severe or salt wasting phenotype. In those women with CAH who do conceive, course and outcome of pregnancy is mostly uneventful, although the rate of SGA offspring may be increased. Psychomotor and somatic long-term development of the children was within normal limits.
据报道,先天性肾上腺皮质增生症(CAH)女性的生育率较低,但相关数据较少。我们评估了CAH女性的妊娠率、妊娠过程、分娩方式及子代的长期结局。
一大群因21-羟化酶缺乏导致CAH的女性最初在一个中心被诊断并接受随访。联系了那些已分娩的女性。从医院记录、直接与患者接触、结构化问卷以及妊娠与预防保健手册中收集信息。
1978年至1998年间,18例CAH女性(1例失盐型、12例单纯男性化型、5例非经典型)生育了31名儿童(18名女性,13名男性)。31名儿童中有16名通过剖宫产分娩。没有女婴出现男性化。29名儿童足月出生,5名儿童小于胎龄(SGA)。所有儿童的产后发育基本正常;18名儿童现已超过10岁,7名儿童年龄在5至10岁之间,6名儿童小于5岁。
CAH女性的生育能力降低,尤其是那些具有严重或失盐型表型的女性。在那些成功受孕的CAH女性中,妊娠过程和结局大多正常,尽管SGA子代的发生率可能会增加。儿童的精神运动和躯体长期发育在正常范围内。