Services / OPA1

Cause of Disease:

Optic Atrophy Type1 (OPA1), is a dominantly inherited optic neuropathy. A mutation in this gene resulting in progressive loss of visual acuity and leading to legal blindness in many cases.

Method of Test:

MLPA - Capillary Electrophoresis.

Type of Sample:

Blood, Amino synthesis, Tissue, Bucal Swab.

Test Duration:

1-2 weeks.