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Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series
Individuals with 22q11.2 deletion syndrome (22q11.2DS) are at elevated risk of developing treatable psychiatric and neurological disorders, including anxiety disorders, schizophrenia, seizures, and movement disorders, often beginning in adolescence or early to mid adulthood. Here, we provide an over...
Tallennettuna:
| Julkaisussa: | Am J Med Genet A |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6209527/ https://ncbi.nlm.nih.gov/pubmed/29777584 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.38708 |
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