Clinical implications and possible association of malposition of the branch pulmonary arteries with DiGeorge syndrome and microdeletion of chromosomal region 22q11

American Journal of Cardiology

Volumn 80, Issue 12, 1997, Pages 1624-1627

  Recto, Michael R ^a   Parness, Ira A ^a   Gelb, Bruce D ^a   Lopez, Leo ^a   Lai, Wyman W ^a  

^a MOUNT SINAI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 22Q; CLINICAL ARTICLE; DIGEORGE SYNDROME; FEMALE; HUMAN; LUNG BLOOD FLOW; MALE; NEWBORN; PRIORITY JOURNAL; PULMONARY ARTERY;

ADOLESCENT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; PULMONARY ARTERY;

EID: 0031437419     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9149(97)00782-0     Document Type: Article

References (20)

1. Jue KL, Lockman LA, Edwards JE. Anomalous origins of pulmonary arteries from pulmonary trunk ("crossed pulmonary arteries"). Am Heart J. 71:1966;807-812.
2. Becker AE, Becker MJ, Edwards JE. Malposition of pulmonary arteries (crossed pulmonary arteries) in persistent truncus arteriosus. AJR Radium Ther Nucl Med. 110:1970;509-514.
3. Ho SY, Wilcox BR, Anderson RH, Lincoln JCR. Interrupted aortic arch-anatomical features of surgical significance. Thorac Cardiovasc Surg. 31:1983;199-205.
4. Wells TR, Takahashi M, Landing BH, Ritchie GW, Ang SM, Diaz JF, Mahnovski V. Branching patterns of right pulmonary artery in cardiovascular anomalies. Pediatric Pathol. 13:1993;213-223.
5. Wolf WJ, Casta A, Nichols M. Anomalous origin and malposition of the pulmonary arteries (crisscross pulmonary arteries) associated with complex congenital heart disease. Pediatr Cardiol. 6:1986;287-291.
6. Goldmuntz E, Driscoll D, Budarf ML, Zackai EH, Mcdonald-McGinn DM, Biegel JA, Emanuel BS. Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects. J Med Genet. 30:1993;807-812.
7. Van Mierop LHS, Kutsche LM. Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. Am J Cardiol. 58:1986;133-137.
8. Goldberg R, Motzkin B, Marion R, Scambler PJ, Shprintzen RJ. Velocardiofacial syndrome a review of 120 patients . Am J Med Genet. 45:1993;313-319.
9. Shprintzen RJ, Goldberg RB, Lewin ML, Sidoti EJ, Berkman MD, Argamaso RV, Young D. A new syndrome involving cleft palate, cardiac anomalies, typical facies and learning disabilities velo-cardio-facial syndrome . Cleft Palate J. 15:1978;56-62.
10. Young D, Shprintzen RJ, Goldberg RB. Cardiac malformations in the velocardiofacial syndrome. Am J Cardiol. 46:1980;643-648.
11. Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11. J Med Genet. 30:1993;822-824.
12. Carey AH, Kelley D, Halford S, Wadey R, Wilson D, Goodship J, Burn J, Paul T, Sharkey A, Dumansky J, Nordenskjold M, Williamson R, Scambler PJ. Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome. Am J Hum Genet. 51:1992;964-970.
13. Desmaze C, Prieur M, Amblard F, Aikem M, Le Deist F, Demezuk S, Zucman J, Plougastel B, Delattre O, Croquette MF, Breviere GM, Huon C, Le Merrer M, Mathieu M, Sidi D, Stephan JL, Aurias A. Physical mapping by FISH of the DiGeorge critical region (DGCR) involvement of the region in familial cases . Am J Hum Genet. 53:1993;1239-1249.
14. Desmaze C, Scambler P, Prieur M, Halford S, Sidi D, Le Deist F, Aurias A. Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization. Hum Genet. 90:1993;663-665.
15. Driscoll DA, Budarf MF, Emanuel BS. A genetic etiology for DiGeorge syndrome consistent deletions and microdeletions of 22q11 . Am J Hum Genet. 50:1992;924-933.
16. Driscoll DA, Spinner NB, Budarf ML, McDonald-McGinn DM, Zackai EH, Goldberg RB, Shprintzen RJ, Saal HM, Zonana J, Jones MC, Mascarello JT, Emanuel BS. Deletions and microdeletions of 22q11 in velo-cardio-facial syndrome. Am J Med Genet. 44:1992;261-268.
17. Hall JG. Catch 22 [editorial]. J Med Genet. 30:1993;801-802.
18. Scambler PJ, Kelly D, Lindsay E, Williamson R, Goldberg R, Shprintzen R, Wilson DI, Goodship JA, Cross IE, Burn J. Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus. Lancet. 339:1992;1138-1139.
19. Wilson DI, Burn J, Scambler P, Goodship J. DiGeorge syndrome part of CATCH-22 . J Med Genet. 30:1993;852-856.
20. Geva T, Sanders SP, Ayres NA, O'Laughlin MP, Parness IA. Two-dimensional echocardiographic anatomy of atrioventricular alignment discordance with situs concordance. Am Heart J. 125:1993;459-464.