eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | 22q11.2 deletion syndrome |
| Symptom | C0033975|psychosis |
| Sentences | 6 |
| PubMedID- 24157393 | Risk factors and the evolution of psychosis in 22q11.2 deletion syndrome: a longitudinal 2-site study. |
| PubMedID- 24063534 | To the best of our knowledge, this is the first case in the japanese population of a patient with schizophrenia-like psychosis to be diagnosed with 22q11.2 deletion syndrome based on clinical symptoms rather than microdeletion studies. |
| PubMedID- 20817203 | The primary objective of the current prospective study was to examine developmental patterns of voxel-by-voxel gray and white matter volumes (gmv, wmv, respectively) that would predict psychosis in adolescents with 22q11.2 deletion syndrome (22q11.2ds), the most common known genetic risk factor for schizophrenia. |
| PubMedID- 22956479 | Changes in occipital lobe gyrification may be an early marker for psychosis in youth with velo-cardio-facial syndrome. |
| PubMedID- 25715178 | Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome. |
| PubMedID- 20052689 | Failure to confirm association between pik4ca and psychosis in 22q11.2 deletion syndrome. |
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