朱伯特综合征:新生儿表现和早期诊断的病例报告
Carla I González-Gordillo1, Leslie E Orozco-Soto1, Juan R Osegueda-Mayen1
1Unidad de Neonatología, Centro Médico ABC, Mexico City.
Boletin medico del Hospital Infantil de Mexico
|July 25, 2023
概括
朱伯特综合征是一种罕见的遗传性疾病,在脑部成像上呈现出特有的"牙标志". 新生儿的早期诊断对于改善结果和生活质量至关重要.
科学领域:
- 遗传学 是一个遗传学.
- 神经学 神经学
- 儿科 儿科 儿科
背景情况:
- 朱伯特综合征是一种罕见的遗传性疾病,每8万至10万名新生儿中就有1例发生.
- 通常以自身相对递归模式遗传,罕见的X链和自身相对主导形式.
- 关键特征包括脑成像中的"牙标志",低血压和发育迟缓.
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