![]() Circulation 26:39–59Ĭeloria GC, Patton RB (1959) Congenital absence of the aortic arch. Roberts WC, Morrow AG, Braunwald E (1962) Complete interruption of the aortic arch. Kirby ML, Turnage KL 3rd, Hays BM (1985) Characterization of conotruncal malformations following ablation of "cardiac" neural crest. Am J Cardiol 30(5):514–525īockman DE, Kirby ML (1984) Dependence of thymus development on derivatives of the neural crest. Rudolph AM, Heymann MA, Spitznas U (1972) Hemodynamic considerations in the development of narrowing of the aorta. ![]() Van Mierop LH, Kutsche LM (1984) Interruption of the aortic arch and coarctation of the aorta: pathogenetic relations. Van Praagh R, Bernhard WF, Rosenthal A, Parisi LF, Fyler DC (1971) Interrupted aortic arch: surgical treatment. Aortic arch anomalies and the pathogenesis of the DiGeorge syndrome. Eur J Pediatr 161(3):173–174īinder M (1985) The teratogenic effects of a bis(dichloroacetyl)diamine on hamster embryos. Ito T, Okubo T, Sato H (2002) Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot. Martin DM, Mindell MH, Kwierant CA, Glover TW, Gorski JL (2003) Interrupted aortic arch in a child with trisomy 5q31.1q35.1 due to a maternal (20,5) balanced insertion. Lewin MB, Lindsay EA, Jurecic V, Goytia V, Towbin JA, Baldini A (1997) A genetic etiology for interruption of the aortic arch type B. Goldmuntz E (2005) DiGeorge syndrome: new insights. Van Mierop LH, Kutsche LM (1986) Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. Am J Cardiol 79(8):1147–1148Ĭonley ME, Beckwith JB, Mancer JF, Tenckhoff L (1979) The spectrum of the DiGeorge syndrome. Powell CB, Stone FM, Atkins DL, Watson DG, Moller JH (1997) Operative mortality and frequency of coexistent anomalies in interruption of the aortic arch. Lancet 1(7899):140–142įyler DC, Buckley LP, Hellenbrand WE, Cohn HE (1980) Report of the New England Regional Infant Cardiac Program. Am J Roentgenol Radium Therapy, Nucl Med 114(2):362–370Įlliott RB, Starling MB, Neutze JM (1975) Medical manipulation of the ductus arteriosus. Gokcebay TM, Batillas J, Pinck RL (1972) Complete interruption of the aorta at the arch. Weisman D, Kesten HD (1948) Absence of transverse aortic arch with defects of cardiac septums report of a case simulating acute abdominal disease in a newborn infant. Steidele RJ (1778) Samml Chir u Med Beob (Vienna) 2:114 Left ventricular outflow tract obstruction.However, IAA remains a surgical challenge, in the acute outcomes and in the late recurrent aortic arch or left ventricular outflow tract obstruction. The operative repair results have improved significantly in the last two decades. The surgical treatment has evolved from a staged approach to a primary surgical repair. The management was greatly improved with the introduction of prostaglandin E1, which allowed for preoperative stabilization. IAA is fatal in the neonatal period, if left untreated. IAA often has a genetic basis and usually occurs in association with other anomalies, especially ventricular septal defect. The location of this interruption is the basis for a widely accepted classification in three types. It consists of a discontinuity between two segments of the aortic arch. Interrupted aortic arch (IAA) is a rare congenital heart disease.
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