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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Detalles Bibliográficos
Autores principales: Kook, So Dahm, An, Suk Kyoon, Kim, Kyung Ran, Kim, Woo Jung, Lee, Eun, Namkoong, Kee
Formato: Texto
Lenguaje:English
Publicado: Korean Neuropsychiatric Association 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848773/
https://www.ncbi.nlm.nih.gov/pubmed/20396437
http://dx.doi.org/10.4306/pi.2010.7.1.72

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848773/
https://www.ncbi.nlm.nih.gov/pubmed/20396437
http://dx.doi.org/10.4306/pi.2010.7.1.72

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