Abstract
A 12 year-old girl presented with cognitive disability and dysmorphic features. Chromosome microarray analysis revealed a de novo, approximately 4.5 Mb terminal deletion of the short arm of chromosome 12 at 12p13.33 region: chr12:100712-4607067. At 13 years this patient developed psychotic manifestations and was admitted to a psychiatric department for treatment. She started hearing voices, talking to herself and laughing without reason. We have previously reported a male individual with psychotic manifestations and a larger (6.2 Mb) terminal deletion in the same chromosomal region. The present case along with previous reports, define a 2 Mb region on chromosome 12p, where a psychosis-associated gene may be located. Included in this psychosis-associated area are 18 OMIM listed genes.
| Original language | English |
|---|---|
| Pages (from-to) | 573-576 |
| Number of pages | 4 |
| Journal | European Journal of Medical Genetics |
| Volume | 55 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 2012 |
| Externally published | Yes |
Keywords
- Developmental delay
- Dysmorphic features
- Growth delay
- Hypermobile joints
- Large incisors
- Long fingers
- Malocclusion
- Microcephaly
- Micrognatia
- Psychosis
- Terminal deletion 12p
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