One-year-old's rare disorder which leaves her always 'starving'
A mother has opened up on her heart-wrenching experience with her daughter's rare condition, Prader-Willi syndrome, which ...
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Gene therapy shows promise in treating SCN1B-linked epileptic encephalopathies
Dravet syndrome and other developmental epileptic encephalopathies are rare but devastating conditions that cause a host of symptoms in children, including seizures, intellectual disability, and even ...
Gene therapy for rare epilepsy shows promise in mice
Dravet syndrome and other developmental epileptic encephalopathies are rare but devastating conditions that cause a host of ...
Mouse model unveils dynamics through which SYNGAP1 gene supports cognitive function
The SYNGAP1 gene, which supports the production of a protein called SynGAP (Synaptic Ras GTPase-Activating Protein), is known ...