在第一位伊朗患者中,由KLHL7基因变异引起的PERCHING综合征:一个病例报告研究
Mousa Ghelichi-Ghojogh1, Saeed Golfiroozi2, Sahar Delavari3
1Neonatal and Children's Health Research Center Golestan University of Medical Sciences, Gorgan, Iran.
Annals of medicine and surgery (2012)
|February 9, 2024
概括
珀奇综合征是一种遗传性疾病,具有发育迟缓和独特的身体特征. 在一个患有低血压和发育迟缓的6个月大的婴儿身上发现了一种特定的KLHL7基因变异,有助于了解这种罕见的疾病.
科学领域:
- 遗传学和分子生物学
- 发育生物学 发展生物学
- 临床医学 临床医学
背景情况:
- 珀奇综合征是一种罕见的遗传性疾病,影响多个身体系统,其特点是发育迟缓,独特的面部特征,食和呼吸困难,生长迟缓,低血压和关节硬.
- 这种综合征是以自身遗传的递归模式遗传的,这意味着父母双方都必须携带改变基因的副本.
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