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胎儿碘综合征

Fetal iodine syndrome

ORPHA:1910疾病

定义 英文原文(暂无中文)

Fetal iodine syndrome refers to symptoms and signs that may be observed in a fetus or newborn when the mother was exposed during pregnancy to inappropriate (insufficient or excessive) amounts of iodine. Iodine deficiency is associated with goiter and hypothyroidism. When severe iodine deficiency occurs during pregnancy, it is associated with congenital hypothyroidism that is manifested by increased neonatal morbi-mortality and severe mental dysfunction, hyperactivity, attention disorders and a substantial decrease of IQ of an irreversible nature. Excessive iodine ingestion during the third trimester of pregnancy can result in hypothyroidism and fetal goiter due to a prolonged inhibition of thyroid hormone synthesis, an increase in thyrotropin (TSH).

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 7

极常见 99–80%4

  • 偏瘫/轻偏瘫 HP:0004374
  • 智力障碍 HP:0001249
  • 感音神经性听力受损 HP:0000407
  • 痉挛性双侧瘫痪 HP:0001264

常见 79–30%1

  • 甲状腺功能减退症 HP:0000821

偶见 29–5%2

  • 眼球震颤 HP:0000639
  • 斜视 HP:0000486

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)