This tends to head to liberal night blindness and visual area constriction. BCD is an uncommon disease and appears to be more popular in folk with Asian descent. People with BCD have crystals in some of their light-colored blood cells (lymphocytes) that can be seen by using an electron microscope.
Their presence does not seem to harm the patient in any other way except to affect vision. BCD is inherited primarily in an autosomal recessive fashion. This means that an influenced person receives one nonworking gene from each of his or her parents. A person who inherits a nonworking gene from only one parent will be a carrier, but will not develop the disease. Bietti’s crystalline dystrophy is inherited primarily in an autosomal recessive fashion. A person with Bietti’s crystalline dystrophy has person received one nonworking gene from each of his or her parents.
However, unless the person has children with addition carrier of BCD genes, the individual’s children are not at risk for developing the disease. There is no treatment for BCD. Gene research will be helpful in finding treatments for patients with BCD. Keeping on Top of Your Condition. Keeping in tune with your disease or condition not only makes treatment less intimidating but also increases its chance of success, and has been shown to lower a patients risk of complications. As well, as an informed patient, you are better able to discuss your condition and treatment options with your physician.