eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | 22q11.2 deletion syndrome |
| Symptom | C0036341|schizophrenia |
| Sentences | 10 |
| PubMedID- 24262682 | Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome. |
| PubMedID- 23916466 | Background: 22q11.2 deletion syndrome (22q11ds) associates with schizophrenia spectrum disorders (ssds), autism spectrum disorders (asds), and other psychiatric disorders, but co-occurrence of diagnoses are not well described. |
| PubMedID- 23248646 | Mirna-mediated risk for schizophrenia in 22q11.2 deletion syndrome. |
| PubMedID- 22078159 | The second finding is the association of schizophrenia with 22q11.2 deletion syndrome (22q11.2ds; also known as velo-cardio-facial syndrome), which has an incidence of 1 in approximately 4,000 live births and leads to a varied set of symptoms, including physical defects and learning disabilities. |
| PubMedID- 26087175 | Purpose: schizophrenia occurs in 20-25% of adults with 22q11.2 deletion syndrome (22q11.2ds). |
| PubMedID- 22214315 | The 1.5 mb region of chromosome 22 associated with 22q11.2 deletion syndrome in schizophrenia is noted by a box. |
| PubMedID- 25484875 | Microrna dysregulation, gene networks, and risk for schizophrenia in 22q11.2 deletion syndrome. |
| PubMedID- 24534796 | Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome. |
| PubMedID- 21475728 | How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome. |
| PubMedID- 21362743 | Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus. |
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