STRA13
Title: Unraveling the Secrets of STRIA13 Gene
Description:
Deep within the intricate tapestry of human DNA lies the STRA13 gene, an enigmatic player in our genetic makeup. This gene holds the key to various biological functions, but its significance extends far beyond that. Let's delve into the fascinating world of STRA13, exploring its role in health, disease, and the cutting-edge research that is unraveling its mysteries.
Associated Diseases:
The STRA13 gene has been linked to several human diseases, including:
- Arthrogryposis Multiplex Congenita (AMC): A rare condition characterized by stiff joints and muscle weakness due to abnormal development in the womb.
- Marfan Syndrome: A connective tissue disorder that affects the heart, eyes, and skeleton, leading to a tall and slender build and potential heart problems.
- Myopathy: A muscle disease that causes weakness and wasting of muscle tissue.
- Congenital Heart Defects: Certain types of heart defects, such as atrial and ventricular septal defects, have been associated with variations in the STRA13 gene.
Did you Know ?
Approximately 1 in 50,000 individuals are affected by Arthrogryposis Multiplex Congenita, making it a relatively rare condition. However, even small changes in the STRA13 gene can have significant implications for the development of this debilitating disorder.
