Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications.

Literature DB >> 11180220

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications.

A Swillen¹, A Vogels, K Devriendt, J P Fryns.

Abstract

In this contribution we review current knowledge of the chromosome 22q11 deletion syndrome, with special emphasis on the clinical characteristics, including physical features, cognitive-behavioral spectrum, and psychiatric complications.

Entities: Disease

Mesh：

Year: 2000 PMID： 11180220 DOI： 10.1002/1096-8628(200022)97:2<128::aid-ajmg4>3.0.co;2-z

Source DB: PubMed Journal: Am J Med Genet ISSN： 0148-7299

Keyword Cloud
Cited

52 in total

Review 1. Endocrinological Manifestations of Sanjad-Sakati Syndrome.

Authors: Masharib Bashar; Muhammad Taimur; Fnu Amreek; Khalid A Sayeed; Amber Tahir
Journal: Cureus Date: 2020-06-22

2. Early language measures associated with later psychosis features in 22q11.2 deletion syndrome.

Authors: Cynthia B Solot; Tyler M Moore; Terrence Blaine Crowley; Marsha Gerdes; Edward Moss; Daniel E McGinn; Beverly S Emanuel; Elaine H Zackai; Sean Gallagher; Monica E Calkins; Kosha Ruparel; Ruben C Gur; Donna M McDonald-McGinn; Raquel E Gur
Journal: Am J Med Genet B Neuropsychiatr Genet Date: 2020-07-27 Impact factor: 3.568

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications.

Review 1. Endocrinological Manifestations of Sanjad-Sakati Syndrome.

2. Early language measures associated with later psychosis features in 22q11.2 deletion syndrome.

Review 3. Genetics of the polymicrogyria syndromes.

Review 4. From microscopes to microarrays: dissecting recurrent chromosomal rearrangements.

5. Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome.

6. Premature death in adults with 22q11.2 deletion syndrome.

7. Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome.

Review 8. Cognitive characteristics of children with genetic syndromes.

9. Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum.

Review 10. Velocardiofacial syndrome: is there a neuropsychiatric phenotype?