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Epilepsy in Christianson syndrome: Two cases of Lennox–Gastaut syndrome and a review of literature
Christianson syndrome (CS) is an X-linked intellectual disorder caused by mutations in the SLC9A6 gene. Clinical features of CS include an inability to speak, truncal ataxia, postnatal microcephaly, hyperkinesis, and epilepsy. Almost all patients with CS develop drug-resistant epilepsy—its most seri...
Sparad:
| I publikationen: | Epilepsy Behav Rep |
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| Huvudupphovsmän: | , , , , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Elsevier
2019
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6920258/ https://ncbi.nlm.nih.gov/pubmed/31879735 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ebr.2019.100349 |
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