马尔凡综合征中的双体性马赛克
Ignacio Arroyo Carrera1, Almudena Amor-Salamanca2, Elena Márquez Isidro1
1Pediatrics Department, San Pedro de Alcántara Hospital, Cáceres, Spain.
American journal of medical genetics. Part A
|August 16, 2024
概括
这项研究报告了马凡综合征 (MFS) 的第一个病例,该病例发生在一个患有FBN1基因中的两种罕见病原性马赛克变异的儿童身上. 这些发现表明,突变发生在发育早期,影响多种组织.
科学领域:
- 遗传学 遗传学 是一个
- 分子生物学分子生物学
- 医学遗传学 医学遗传学
背景情况:
- 马凡综合征 (MFS) 是一种由FBN1基因变异引起的遗传性结合组织疾病.
- 它影响心血管,眼睛和骨系统,通过根特鼻科诊断.
- 临床变异性是MFS的一个标志.
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