Conditions / Genetic
gelatinous drop-like corneal dystrophy
info ยท Genetic
An epithelial and subepithelial dystrophy that is characterized by severe corneal amyloidosis leading to blindness and that has_material_basis_in homozygous or compound heterozygous mutation in the TACSTD2 gene which encodes the monoclonal antibody-defined, tu
An epithelial and subepithelial dystrophy that is characterized by severe corneal amyloidosis leading to blindness and that has_material_basis_in homozygous or compound heterozygous mutation in the TACSTD2 gene which encodes the monoclonal antibody-defined, tumor-associated antigen GA733-1, on chromosome 1p32.
Signs and symptoms
- Corneal foreign body sensation
- Corneal dystrophy
- Photophobia
- Reduced visual acuity
- Visual impairment
- Blurred vision
Also known as: GDCD; corneal amyloidosis; primary familial amyloidosis of the cornea; subepithelial amyloidosis of the cornea