Patent Ductus Arteriosus 3; Pda3
The ductus arteriosus is a vital in utero vascular connection between the aorta and pulmonary artery that allows right ventricular output to bypass the nonventilated fetal lungs. Postnatal closure of the ductus arteriosus is an important step in normal cardiopulmonary transition. Failure of ductal closure results in patent ductus arteriosus (PDA), which occurs in approximately 2 to 8 per 10,000 term infants and constitutes 5% to 7% of all congenital heart defects (summary by Hajj and Dagle, 2012).For a discussion of genetic heterogeneity of isolated PDA, see PDA1 (OMIM ).
Genes related to Patent Ductus Arteriosus 3; Pda3
Clinical FeaturesPhenotypes and symptoms related to Patent Ductus Arteriosus 3; Pda3
- Ventricular septal defect
- Congestive heart failure
- Patent ductus arteriosus
- Abnormal heart morphology
- Hypoplastic left heart
- Pulmonary artery stenosis
Incidence and onset information— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Patent Ductus Arteriosus 3; Pda3 Recommended genes panels
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BCL6, RHEB, RIPK1, RIPK2, RIPK3, RIT1, BCL7A, BCL9, BCR, ROBO2, ROCK1, ROCK2, ROR1, ROR2, ROS1, RPA1, BDNF, RPL5, RPN1, RPS6KB1 , (...)
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Sources and references
You can check the following sources for additional information.OMIM Rare Disease Search Engine
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