Campomelic Syndrome Treatment: Advances in Prenatal Diagnosis and Market Trends
Campomelic syndrome, also known as campomelic dysplasia, is a rare and severe congenital skeletal disorder characterized by bowing of the long bones, distinctive facial features, and multiple systemic abnormalities. The condition is primarily caused by mutations in the SOX9 gene, which plays a crucial role in skeletal development and sex differentiation. Although campomelic syndrome...
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