Axenfeld-Rieger syndrome (ARS)is an autosomal dominant disorder that presents with both ocular and … 展开

Peters anomaly is a congenital disease heterogeneously affecting the anterior segment, often presenting with a central corneal opacity and a defect in the endothelium and Descemet’s membrane of the cornea; the p… 展开

PCGis an autosomal recessive disorder defined as having elevated IOP at or within 2 years of birth. It is considered to be a part of ASD as it frequently involves malformations of the structures involved in aqueous humor … 展开

Aniridia is an autosomal dominant disorder that involves a variety of ocular manifestations, usually without systemic symptoms, that include but are not limited to: iris hypoplasia, lens dislocation, and corneal opacity.I… 展开

Congenital hereditary endothelial dystrophy (CHED)is an autosomal recessive (CHED Type 2) disease that often presents as congenital corneal edema with bilateral corneal opacifications. Molecular and Developmental … 展开