Familial whole Exome Sequencing to Identify Genetic Variants Associated with Polycystic Ovarian Syndrome in Indians
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Abstract
Polycystic Ovary Syndrome (PCOS) is an endocrinological gynecology disorder with heterogeneous representation of the clinical symptoms among its patients. Due to this dynamic nature there is a lack of consensus in the medical community for the diagnosis and treatment. The pathophysiology not being clearly understood adds on to the discrepancies. Genetics has been reported to be a major etiology of PCOS, which is a complex disorder following a non-mendelian pattern of inheritance
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