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羊水过少序列征(波特综合征):田纳西州东北部的病例聚集情况

Oligohydramnios sequence (Potter's syndrome): case clustering in northeastern Tennessee.

作者信息

Prouty L A, Myers T L

出版信息

South Med J. 1987 May;80(5):585-92.

PMID:3576270
Abstract

The oligohydramnios sequence (OS) is manifest in newborns when prolonged oligohydramnios has been present during pregnancy. The most important signs are an infant small for gestational age, with wrinkled skin, Potter facies, compression deformities of the limbs, and respiratory distress caused by pulmonary hypoplasia. The recurrence rate of kidney conditions implicated in OS depends on the severity of the condition in the previously affected sib. While absent or encysted kidneys (Potter types II and IV) are incompatible with life, chronic leakage of amniotic fluid may result in a viable infant who shows some signs of OS. The usual incidence of absent or encysted kidneys is 1 per 6,250 births. This rate was exceeded recently in northeastern Tennessee, in a clustering of cases for which no environmental causes are evident.

摘要

羊水过少序列征(OS)在孕期出现长时间羊水过少时会在新生儿中表现出来。最重要的体征是小于胎龄儿,皮肤有皱纹,波特面容,肢体受压畸形,以及肺发育不全引起的呼吸窘迫。与羊水过少序列征相关的肾脏疾病复发率取决于先前患病同胞中病情的严重程度。虽然无肾或肾囊肿(波特Ⅱ型和Ⅳ型)无法存活,但羊水慢性渗漏可能会导致一个有存活能力的婴儿出现一些羊水过少序列征的体征。无肾或肾囊肿的通常发病率为每6250例出生中有1例。最近在田纳西州东北部,在一组无明显环境病因的病例聚集区,这一发病率超过了该数值。

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