Recent studies have revealed that a genetic mutation of the gene responsible for Raynaud’s phenomenon, a disorder characterized by abnormal constriction and dilation of blood vessels, can now be identified. This discovery could lead to improved diagnosis and treatments for this condition.

For those who suffer from Raynaud’s phenomenon, a new breakthrough in genetics could offer hope for better treatments and diagnosis. Recent studies have identified a genetic mutation responsible for the disorder, which causes abnormal constriction and dilation of blood vessels. This discovery is a major breakthrough in understanding the cause of the disorder, and could open up new possibilities for improved diagnosis and treatments for those suffering from this condition.

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source: Phys.org