Midline brain anomalies in a young schizophrenic patient with 22q11 deletion syndrome
β Scribed by Soyoung Irene Lee; Han-Yong Jung; Seung-Hyun Kim; Doh Kwan Kim; Jioh Mok
- Book ID
- 119554891
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 111 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0920-9964
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Skeletal anomalies in patients with a 22q11.2 deletion are reported infrequently. We report the skeletal findings in 108 patients with a 22q11.2 deletion, of whom 37 (36%) had a skeletal anomaly. Twenty-two patients (20%) had anomalies of the limbs, 7 of the upper limb, including preaxial or postaxi
## Abstract 22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affecting humans. The syndrome is associated with general cognitive impairments and specific deficits in visualβspatial ability, nonβverbal reasoning, and planning skills. 22q11DS is also associated wi