在中国南部患有洛氏综合征的患者中,非典型的表型和新的OCRL变异

Rong Du1,2, Chengcheng Zhou1, Shehong Chen1,3

  • 1Department of Genetics and Endocrinology, Guangzhou Women and Children's Medical Center, Guangdong Provincial Clinical Research Center for Child Health, National Children's Medical Center for South Central Region, Guangzhou Medical University, Guangzhou, 510623, China.

概括

洛伊综合征是一种遗传性疾病,可以在没有先天性白内障的情况下呈现异常. 这项研究在中国患者中发现了新型的OCRL基因变异,揭示了洛伊综合征遗传多样性和临床谱的新见解.

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