Duplication 15q11-q13 Syndrome
Autosomal dominant abnormalities of chromosome 15q: features of the chromosome 15q11-q13 duplication syndrome include AUTISM SPECTRUM DISORDER; INTELLECTUAL DISABILITY; ATAXIA, seizures, developmental delays, and behavioral problems. OMIM: 608636. A heterozygous deletion of chromosome 15q11.2 may increase the susceptibility to neuropsychiatric or neurodevelopmental problems, including delayed psychomotor development, speech delay, ATTENTION DEFICIT-HYPERACTIVITY DISORDER; OBSESSIVE-COMPULSIVE DISORDER, and possibly seizures. OMIM: 615656
Also Known As:
15q11.2 microdeletion; Chromosome 15q11-q13 Duplication Syndrome; Chromosome 15q11.2 deletion syndrome; Microdeletion 15q11.2
Networked: 3
relevant articles (0 outcomes,
0 trials/studies)
Disease Context: Research Results
Related Diseases
Experts
1. | Chang, Shu-Yuan:
1 article
(10/2018)
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2. | Chang, Tung-Yao:
1 article
(10/2018)
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3. | Chen, Chih-Ping:
1 article
(10/2018)
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4. | Chen, Li-Feng:
1 article
(10/2018)
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5. | Chen, Shin-Wen:
1 article
(10/2018)
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6. | Chern, Schu-Rern:
1 article
(10/2018)
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7. | Chuang, Tzu-Yun:
1 article
(10/2018)
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8. | Lai, Shih-Ting:
1 article
(10/2018)
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9. | Town, Dai-Dyi:
1 article
(10/2018)
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10. | Wang, Liang-Kai:
1 article
(10/2018)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Duplication 15q11-q13 Syndrome: