22q11.2 DS syndrome as a genetic subtype of schizophrenia
Introduction The 22q11.2 deletion syndrome (22q11.2 DS) is associated with the microdeletion of this chromosomal region, and represents the second most common genetic syndrome after Down's syndrome. In patients with schizophrenia, 22q11.2 DS has a prevalence of 2%, and in selected groups can be...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2015
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/23050
- Acceso en línea:
- https://doi.org/10.1016/j.rcp.2014.09.002
https://repository.urosario.edu.co/handle/10336/23050
- Palabra clave:
- Article
Birth defect
Chromosome deletion 22q11
Chromosome deletion 22q11.2
Clinical feature
Clinical practice
Down syndrome
Fluorescence in situ hybridization
Genetic association
Genetic disorder
Genetic risk
Human
Medical record review
Mental disease
Molecular genetics
Morbidity
Multiplex ligation dependent probe amplification
Phenotype
Polymerase chain reaction
Schizophrenia
Digeorge syndrome
Genetic counseling
Genetic predisposition
Genetics
Psychology
Schizophrenia
Digeorge Syndrome
Genetic Counseling
Genetic Predisposition to Disease
Humans
Phenotype
Schizophrenia
22q11.2 deletion syndrome
22q11.2 microdeletion
22q11.2DS
Schizophrenia
- Rights
- License
- Abierto (Texto Completo)