|Title:||Persistent Fifth Aortic Arch Associated with 22q11.2 Deletion Syndrome||Authors:||李美慧
|Keywords:||aortic arch syndrome;conotruncal cardiac malformation;human;UFDIL protein||Issue Date:||2006||Journal Volume:||v.105||Journal Issue:||n.4||Start page/Pages:||284-289||Source:||JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION||Abstract:||
Background: Chromosome 22q 11.2 deletion is frequently associated with conotruncal malformations and aortic arch anomalies. This study investigated the association of chromosome 22q 11.2 deletion with clinical manifestations in four pediatric patients with persistent fifth aortic arch. Methods: Four patients with persistent fifth aortic arch treated between July 1997 and June 2004 were included in this retrospective study. There were two girls and two boys, aged 2 days to 11.3 years, with persistent fifth aortic arch and cardiac conotruncal malformations. Chart recordings , plain chest films, two-dimensional and Doppler echocardiograms, cardiac catheterization with angiograms, surgical findings, and cytogenetic study were analyzed. Results: Clinically, all four patients had the cardinal phenotypic features of 22q 11.2 deletion syndrome, including cardiovascular malformations (conotruncal malformations and aortic arch anomalies), abnormal facies, thymic hypoplasia, canopy anomaly of the palate (high-arched palate, rather than cleft palate), and hypocalcemia (or hypoparathyroidism) . All four patients were confirmed to have chromosome 22q 11 .2 deletion. Conclusion: Congenital conotruncal malformations, including tetralogy of Fallot with pulmonary atresia or stenosis, and aortic arch anornalies including a persistent Fifth aortic arch or a right aortic arch, should lead to suspicion of chromosome 22q 11.2 deletion when manifested together with any one of the other four cardinal phenotypic features.
|Appears in Collections:||醫學系|
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