HLHS with severe aortic insufficiency in a patient with 45,X/46,XY mosaicism

Annals of Thoracic Surgery

Volumn 78, Issue 4, 2004, Pages 1475-1476

  Mumtaz, Muhammad A ^a   Mee, Roger B B ^a   Qureshi, Athar ^a   Patel, Chandrakant R ^b   Younoszai, Adel K ^a  

^a LERNER RESEARCH INSTITUTE   (United States)

^b AKRON CHILDREN'S HOSPITAL   (United States)

Author keywords

21

Indexed keywords

AORTA VALVE REGURGITATION; ARTICLE; CASE REPORT; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; MALE; NEWBORN; PRIORITY JOURNAL; SEX CHROMOSOME MOSAICISM; SURGICAL TECHNIQUE; SUTURING METHOD; TREATMENT OUTCOME;

ADULT; AORTIC VALVE INSUFFICIENCY; CARDIAC SURGICAL PROCEDURES; CHROMOSOMES, HUMAN, X; CHROMOSOMES, HUMAN, Y; FEMALE; FONTAN PROCEDURE; HUMANS; HYPOPLASTIC LEFT HEART SYNDROME; INFANT, NEWBORN; MALE; MITRAL VALVE INSUFFICIENCY; MONOSOMY; MOSAICISM; PREGNANCY; PREGNANCY COMPLICATIONS; SEX CHROMOSOME DISORDERS;

EID: 4644284666     PISSN: 00034975     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.athoracsur.2003.07.004     Document Type: Article

References (4)

1. Razzouk A.J., Chinnock R.E., Gundry S.R., et al. Transplantation as a primary treatment for hypoplastic left heart syndrome intermediate term results. Ann Thorac Surg. 62:1996;1-7
2. Gaynor J.W., Mahle W.T., Cohen M.I., et al. Risk factors for mortality after Norwood procedure. Eur J Cardiothorac Surg. 22:2002;82-89
3. Chang H.J., Clark R.D., Bachman H. The phenotype of 45,X/46,XY mosaicism an analysis of 92 prenatally diagnosed cases. Am J Hum Genet. 46:1990;156-167
4. Krasemann T., Kehl H.G., Hammel D., Asfour B. Congenital aortic regurgitation due to absent aortic cusps and high degree mitral stenosis. Pediatr Cardiol. 24:2003;304-306