Alagille Syndrome Market

Aishwarya Bhasme31 Jul, 2024Business

Alagille syndrome is an exceptional autosomal leading genetic disorder that affects many organ systems of the body usually in the skeleton, liver, eyes, kidneys, and heart. Alagille syndrome is initiated by either change in the JAG1 gene or deletion in gene material on chromosome 20 that contains the JAG1 genetic factor. These proteins are essential for Notch signalling between neighbouring cells throughout embryonic development and error in genetic factor results in abnormalities in the heart, bile ducts, certain facial features, and spinal column.