Heterogene neuropsychiatrische Phänotypen bei zwei erwachsenen Patient*innen mit 22q11.2-Deletionssyndrom (DiGeorge-Syndrom): ein Fall für RDoC?

DiGeorge’s syndrome is one of the most frequent microdeletion syndromes and is associated with a high risk for neuropsychiatric disorders of intelligence, social communication and executive functioning as well as psychotic disorders. The male patient described here represents one of the rare descrip...

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Detalles Bibliográficos
Autores principales: Praus, Peter, Braun, Urs, Bleich, Melanie, Meyer-Lindenberg, Andreas, Hennig, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Medizin 2021
Materias:
Originalien
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061649/
https://www.ncbi.nlm.nih.gov/pubmed/34735587
http://dx.doi.org/10.1007/s00115-021-01226-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061649/
https://www.ncbi.nlm.nih.gov/pubmed/34735587
http://dx.doi.org/10.1007/s00115-021-01226-6

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