What does BFFR mean in UNCLASSIFIED
Benign Familial Fleck Retina (BFFR) is a rare condition, which causes the appearance of yellowish spots or flecks on the retina. These flecks can cause vision problems such as difficulty with night vision and loss of peripheral vision. BFFR is caused by genetic mutations and usually affects multiple members in a family, making it an inherited condition.
BFFR meaning in Unclassified in Miscellaneous
BFFR mostly used in an acronym Unclassified in Category Miscellaneous that means Benign Familial Fleck Retina
Shorthand: BFFR,
Full Form: Benign Familial Fleck Retina
For more information of "Benign Familial Fleck Retina", see the section below.
Essential Questions and Answers on Benign Familial Fleck Retina in "MISCELLANEOUS»UNFILED"
What is Benign Familial Fleck Retina?
Benign Familial Fleck Retina (BFFR) is a rare condition that causes yellowish spots or flecks to appear on the retina, resulting in vision problems including difficulty with night vision and loss of peripheral vision.
How is BFFR inherited?
BFFR is usually inherited from parent to child, meaning multiple members of a family may be affected by the condition. It is caused by genetic mutations passed down from generation to generation.
What are the symptoms of BFFR?
The main symptom of BFFR are yellowish spots or flecks on the retina, which can cause decreased vision such as difficulty seeing at night or loss of peripheral vision.
Can BFFR be treated?
There currently are no known treatments for BFFR, however some people may not experience any symptoms at all while others may need glasses or contact lenses to help improve their vision. Regular eye tests should be done in order to monitor any changes in sight.
Who is at risk for developing BFFR?
Those who have other family members with the condition are at higher risk for developing BFFR due to its hereditary nature. However, it can also happen spontaneously without being directly inherited from parents or grandparents.
Final Words:
Benign Familial Fleck Retina (BFFR) is a rare condition that affects multiple family members due to its hereditary nature and can lead to visual problems such as difficulty with night vision and reduced peripheral sight. While there currently are no treatments for this disorder regular eye tests should be done in order to monitor any changes in sight.