吲哚美辛胚胎胎儿病
Indomethacin embryofetopathy
ORPHA:1909疾病
定义 英文原文(暂无中文)
Indomethacin embryofetopathy refers to the manifestations that may be observed in a fetus or newborn when the mother has taken indomethacin, a potent prostaglandin inhibitor and tocolytic agent that can cross placenta, during pregnancy. Reported adverse fetal/neonatal effects include decreased renal function resulting in oligohydramnios, closure of the ductus arteriosus, and delayed cardiovascular adaptation at birth. These effects are usually transient and reversible. Indomethacin may also be a risk factor for cerebral injury (periventricular leukomalacia) and necrotizing enterocolitis in preterm infants.
别名
胎儿吲哚美辛综合征
基本事实
- 遗传方式
- 不适用
- 发病年龄
- 产前、新生儿期
临床表型 12
极常见 99–80%4
- 肾病 HP:0000112
- 早产 HP:0001622
- 肾功能不全 HP:0000083
- 呼吸功能不全 HP:0002093
偶见 29–5%8
- 肾小管形态异常 HP:0000091
- 凝血异常 HP:0001928
- 房间隔缺损 HP:0001631
- 心肌病 HP:0001638
- 胎儿水肿 HP:0001789
- 多囊性肾发育不良 HP:0000003
- 羊水过少 HP:0001562
- 室间隔缺损 HP:0001629
外部标识与链接
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本页数据来源
- 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
- 中文病名:Orphanet 中文包,冻结于 2020-06-01
- 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)