Tuberous sclerosis complex presenting as convulsive status epilepticus followed by hypoxic cerebropathy: A case report

RATIONALE: Tuberous sclerosis complex (TSC) is a relatively rare, autosomal dominant, and progressive neurocutaneous disorder involving multiple organs. Heterozygous mutations in the TSC1 gene located on chromosome 9 (9q34.13) or the TSC2 gene located on chromosome 16 (16p13.3) have been shown to be...

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Detalles Bibliográficos
Autores principales: Liu, Xuncan, Zhang, Yanfeng, Hao, Yunpeng, Chen, Yinbo, Chen, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531247/
https://www.ncbi.nlm.nih.gov/pubmed/31083211
http://dx.doi.org/10.1097/MD.0000000000015545

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531247/
https://www.ncbi.nlm.nih.gov/pubmed/31083211
http://dx.doi.org/10.1097/MD.0000000000015545

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