Stewart-Morel Syndrome: Decoding Rare Genetic Pathways
Stewart-Morel Syndrome Introduction to Stewart-Morel Syndrome Stewart-Morel Syndrome (SMS) is a profoundly rare, inherited genetic disorder characterized by a distinctive constellation of clinical features, primarily encompassing global developmental delays, unique facial dysmorphism, and a range of other characteristic physical attributes. This condition, though infrequent, significantly impacts the developmental trajectory and overall well-being of affected individuals. […]