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Patent arterial duct.
Orphanet J Rare Dis. 2009 Jul 10;4:17. doi: 10.1186/1750-1172-4-17.
Orphanet J Rare Dis. 2009.
PMID: 19591690
Free PMC article.
Review.
Rare families with isolated PAD have been described in which the mode of inheritance appears to be dominant or recessive. Familial incidence of PAD has also been linked to Char syndrome, familial thoracic aortic aneurysm/dissection associated with patent arterial du …
Rare families with isolated PAD have been described in which the mode of inheritance appears to be dominant or recessive. Familial incidence …
Familial nonsyndromic patent ductus arteriosus caused by mutations in TFAP2B.
Chen YW, Zhao W, Zhang ZF, Fu Q, Shen J, Zhang Z, Ji W, Wang J, Li F.
Chen YW, et al.
Pediatr Cardiol. 2011 Oct;32(7):958-65. doi: 10.1007/s00246-011-0024-7. Epub 2011 Jun 4.
Pediatr Cardiol. 2011.
PMID: 21643846
Mutations in TFAP2B, which encodes a neural crest-derived transcription factor, can cause Char syndrome, characterized by PDA, facial dysmorphism, and skeletal abnormalities of the hand. ...
Mutations in TFAP2B, which encodes a neural crest-derived transcription factor, can cause Char syndrome, characterized by PDA, …
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