胎儿米诺地尔综合征
Fetal minoxidil syndrome
ORPHA:1918疾病
定义 英文原文(暂无中文)
Fetal minoxidil syndrome is characterized by a group of symptoms that may be observed in a fetus or newborn when the mother has taken minoxidil during pregnancy. Minoxidil is used in the treatment of malignant renal hypertension and as a topical solution to induce scalp hair growth. Hypertrichosis that gradually diminishes during the first six postnatal months has been reported. Additional reported features include cardiac (congenital great vessel transposition and pulmonary valve stenosis), neurodevelopmental (caudal regression sequence), gastrointestinal, renal, and limb malformations. Conclusive studies are however not available.
别名
米诺地尔所致产前感染
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 8
极常见 99–80%8
- 第五指屈指畸形 HP:0004209
- 隐睾 HP:0000028
- 鼻梁塌陷 HP:0005280
- 全身性多毛症 HP:0002230
- 小下颌 HP:0000347
- 后旋耳 HP:0000358
- 脐疝 HP:0001537
- 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)