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Congenital X-linked adrenal hypoplasia.

作者信息

Hensleigh P A, Moore W V, Wilson K, Tulchinsky D

出版信息

Obstet Gynecol. 1978 Aug;52(2):228-32.

PMID:150559
Abstract

Fetal adrenal hypoplasia should be considered in pregnant patients with family histories of the condition and/or following observation of drastically reduced maternal estriol excretion. Antepartum diagnosis is important in the clinical management of these infants since deteriorating adrenal function frequently follows an asymptomatic period during the early neonatal life. Antepartum and neonatal diagnostic studies can identify fetal adrenal hypoplasia.

摘要

相似文献

1
Congenital X-linked adrenal hypoplasia.
Obstet Gynecol. 1978 Aug;52(2):228-32.
2
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引用本文的文献

1
Prenatal diagnosis of congenital lipoid adrenal hyperplasia (CLAH) by molecular genetic testing in Korean siblings.通过分子遗传学检测对韩国家族性先天性脂质性肾上腺增生症(CLAH)进行产前诊断。
Yonsei Med J. 2011 Nov;52(6):1035-8. doi: 10.3349/ymj.2011.52.6.1035.
2
Familial X-linked adrenocortical hypoplasia association with androgenic precocity.家族性X连锁肾上腺皮质发育不全与雄激素性早熟相关。
Arch Dis Child. 1981 Aug;56(8):633-6. doi: 10.1136/adc.56.8.633.
3
Review: placental sulphatase deficiency.
J Inherit Metab Dis. 1982;5(3):164-76. doi: 10.1007/BF01800173.
4
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.先天性肾上腺发育不全、肌病与甘油激酶缺乏症:缺失的分子遗传学证据
Am J Hum Genet. 1987 Mar;40(3):212-27.