Pulmonary arterial aneurysm with CATCH 22 syndrome: A case report

Angiology

Volumn 52, Issue 11, 2001, Pages 789-791

  Kinoshita, Osamu ^a   Mizoue, Tetsuro ^a   Kusama, Akitoshi ^a   Gomi, Eiichi ^a   Sato, Shinobu ^a   Hongo, Minoru ^a   Kubo, Keishi ^a  

^a SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AORTA ANEURYSM; AORTOPULMONARY SEPTAL DEFECT; ARTICLE; CASE REPORT; CATCH 22 SYNDROME; CHROMOSOME 22Q; CONGENITAL HEART MALFORMATION; DEVELOPMENTAL DISORDER; DIFFERENTIAL DIAGNOSIS; FALLOT TETRALOGY; FEMALE; GENETIC DISORDER; HEART VENTRICLE SEPTUM DEFECT; HEMIZYGOSITY; HUMAN; LIFE EXPECTANCY; LUNG CANCER; MEDIASTINUM TUMOR; PATENT DUCTUS ARTERIOSUS; PULMONARY ARTERY ANEURYSM; SYNDROME DELINEATION; THORAX RADIOGRAPHY;

ADULT; ANEURYSM; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENE DELETION; HUMANS; PULMONARY ARTERY; SYNDROME; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0035212173     PISSN: 00033197     EISSN: None     Source Type: Journal    
DOI: 10.1177/000331970105201110     Document Type: Article

References (6)

1. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2 deletion
2. Velo-cardiofacial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus
3. Discussions on a new concept of the cellular basis of immunology
4. Deletions within chromosome 22q11 in familial congenital heart disease
5. Prevalence of 22q11 microdeletions in DiGeorge and velo-cardiofacial syndromes: Implications for genetic counseling and prenatal diagnosis
6. Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis versus ventricular septal defect with pulmonary atresia