| Epilepsy Model | Acroscell is experienced in epilepsy research with keeping many mouse models of epilepsy caused by of ion channel genes mutations. Both multiple genes mutations and single-gene perturbations induced epilepsy models are available in Acroscell. Our large variety of mouse models can help researchers in understanding epilepsy and drug therapy in epilepsy disorders. These models also help us to discover the genes that cause epilepsy in human patients as well as those genes that have an effect on our susceptibility to seizures. |
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Epilepsy Model
| Autoimmune Autonomic Ganglionopathy | Autoimmune autonomic ganglionopathy (AAG) is an immune-mediated acquired autonomic dysfunction disease that is related to auto-acetylcholine receptor antibodies and mainly manifests as autonomic dysfunction. The disease mostly occurs in young and middle-aged patients, and it often has prodromal symptoms such as respiratory or digestive tract infections, mainly manifested as impaired sympathetic nerve function, such as orthostatic hypotension, syncope, sweatlessness and other glandular secretory dysfunction; paraautonomic dysfunction, such as dry mouth, dry eyes, pupils with slow light reflection, bladder dysfunction, etc.; |
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