期刊
EUROPEAN JOURNAL OF HUMAN GENETICS
卷 20, 期 10, 页码 1011-1017出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/ejhg.2012.100
关键词
aniridia; PAX6; eye; iris; foveal hypoplasia; WAGR syndrome
资金
- Medical Research Council [MC_PC_U127527199, MC_U127527199] Funding Source: Medline
- MRC [MC_PC_U127527199, MC_U127527199] Funding Source: UKRI
- Medical Research Council [MC_PC_U127527199, MC_U127527199] Funding Source: researchfish
Aniridia is a rare congenital disorder in which there is a variable degree of hypoplasia or the absence of iris tissue associated with multiple other ocular changes, some present from birth and some arising progressively over time. Most cases are associated with dominantly inherited mutations or deletions of the PAX6 gene. This article will review the clinical manifestations, the molecular basis including genotype-phenotype correlations, diagnostic approaches and management of aniridia.
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