## Abstract The 22q11 chromosomal deletion syndrome (22q11DS) is associated with a heterogeneous physical phenotype, neurocognitive deficits, and increased risk of later psychiatric illness. Sporadic clinical reports suggested motor differences, but quantitative studies of movement in children with
Presenting phenotype in 100 children with the 22q11 deletion syndrome
✍ Scribed by Sólveig Óskarsdóttir; Christina Persson; Bengt O. Eriksson; Anders Fasth
- Publisher
- Springer
- Year
- 2004
- Tongue
- English
- Weight
- 287 KB
- Volume
- 164
- Category
- Article
- ISSN
- 0340-6997
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📜 SIMILAR VOLUMES
22q11 deletion syndrome (22qDS) is due to microdeletions of chromosome region 22q11.2. Little is known about the phenotype of adults. We reviewed available case reports of adults (age ≥18 years) with 22qDS and compared the prevalence of key findings to those reported in a large European survey of 22
## Abstract There is an overwhelming evidence that children and adults with 22q11.2 deletion syndrome (22q11.2DS) have a characteristic behavioral phenotype. In particular, there is a growing body of evidence that indicates an unequivocal association between 22q11.2DS and schizophrenia, especially
Genetic syndromes associated with deletions at chromosome 22q11 generally have been diagnosed during childhood based on a constellation of physical features. To investigate a reported association of velocardiofacial syndrome with psychotic disorders in adults, we assessed subjects with DSM-IV schizo