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Developmental progression of intellectual disability, autism, and epilepsy in a child with an IQSEC2 gene mutation
The neurodevelopmental progression of a school‐aged child with a spontaneous IQSEC2 mutation has demonstrated apparent regression of milestones and language. Seizures associated with the disorder have been refractory to medical treatment. Late treatment of autism in this child has led to improved so...
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| Vydáno v: | Clin Case Rep |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5628232/ https://ncbi.nlm.nih.gov/pubmed/29026562 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1139 |
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