Congenital, Hereditary, and Neonatal Diseases and Abnormalities: News and Research on Chromosome Disorders

MeSH tree: C16.131.260

New drug target identified for Fragile X syndrome

UCLA Health researchers have identified a potential drug target for treating Fragile X syndrome, the most common genetic cause of intellectual disability and autism that affects roughly one in 2,000 boys.

From fear to trust: How music is transforming dental care

Treating patients who have spent years—sometimes decades—avoiding dental care because of fear, disability, trauma or painful past experiences can be challenging. "They are afraid and don't want to be treated," said Adela ...

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