A case of neonatal encephalopathy with non-epileptic myoclonus mimicking a congenital CMV-infection. How could two different pathologies result in a similar MRI phenotype?
KCNQ2-related disorders are rare autosomal dominant channelopathies caused by mutations in KCNQ2, a gene that encodes a subunit of the voltage-gated potassium channel Kv7, resulting in variable phenotypes. Neonatal encephalopathy
Authors
- Camilla Russo (ORCID: https://orcid.org/0000-0002-2256-7281)
Publication Details
- Journal
- Journal of Clinical Images and Medical Case Reports
- Published
- 2025-04-01
- DOI
- https://doi.org/10.52768/2766-7820/3554
- Primary Topic
- Neurological and metabolic disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00