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Psychotic Features as the First Manifestation of 22q11.2 Deletion Syndrome
The 22q11.2 deletion is a genetic disorder which is characterized by abnormalities in cardiac functioning, facial structure, neurobehavioral development, T cell functioning, and velopharyngeal insufficiencies. In the presented case study, 22q11.2 deletion was found in a patient who has psychotic sym...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Korean Neuropsychiatric Association
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2848773/ https://ncbi.nlm.nih.gov/pubmed/20396437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4306/pi.2010.7.1.72 |
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