Conotruncal cardiac defects
Congenital heart abnormalities that are characterized by AORTIC COARCTATION; DOUBLE-OUTLET RIGHT VENTRICLE, and atrioventricular canal defects. SYNDACTYLY and POLYDACTYLY may also occur. Mutations in several genes have been identified, including CFC1, GDF1, NKX2-5, NKX2-6, TBX-1, and GATA6. OMIM: 217095
Also Known As:
Conotruncal heart malformations
Networked: 6
relevant articles (0 outcomes,
1 trials/studies)
Disease Context: Research Results
Experts
1. | Barutcu, Umit B:
1 article
(03/2017)
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2. | Kundak, Afsin A:
1 article
(03/2017)
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3. | Okumus, Nurullah:
1 article
(03/2017)
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4. | Orun, Utku A:
1 article
(03/2017)
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5. | Ozdemir, Semra:
1 article
(03/2017)
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6. | Pektas, Ayhan:
1 article
(03/2017)
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7. | Zenciroglu, Aysegul:
1 article
(03/2017)
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8. | Lewandowski, Laura B:
1 article
(03/2013)
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9. | Sanghavi, Darshak:
1 article
(03/2013)
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10. | Goldmuntz, Elizabeth:
1 article
(12/2008)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Conotruncal cardiac defects: