皮特 - 霍普金斯综合征中的复杂突:双胞胎病例报告
José Roberto Tude Melo1,2, Ana Rita de Luna Freire Peixoto3, Danilo Marden de Lima Souza3
1D'Or Institute for Research and Education (IDOR), Salvador da Bahia, Brazil.
Pediatric neurosurgery
|January 21, 2024
概括
皮特-霍普金斯综合征 (PTHS) 是一种罕见的遗传疾病. 这份报告详细介绍了两名患有PTHS和复杂突症的婴儿,表明需要进一步调查的潜在联系.
科学领域:
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
- 神经学 神经学
背景情况:
- 皮特-霍普金斯综合征 (PTHS) 是一种罕见的遗传疾病,由TCF4基因变异引起,其特征是神经发育问题和面异常.
- 这项研究侧重于两名被诊断患有PTHS的双胞胎婴儿.
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