Literature DB >> 9339511

The rare association of tetralogy of Fallot with hypertrophic cardiomyopathy. Report of 2 neonatal patients.

M B Lewin1, J A Towbin, M K Thapar, W J Dreyer, T F Feltes.   

Abstract

Although tetralogy of Fallot is commonly associated with other congenital heart defects, it is rarely found in conjunction with hypertrophic cardiomyopathy. We describe the cases of 2 neonates with this rare condition, both of whom required surgical intervention during infancy. Because hypertrophic cardiomyopathy is frequently familial, and tetralogy of Fallot is commonly found in patients diagnosed with chromosomal anomalies, we speculate about a possible genetic cause for this association.

Entities:  

Mesh:

Year:  1997        PMID: 9339511      PMCID: PMC325446     

Source DB:  PubMed          Journal:  Tex Heart Inst J        ISSN: 0730-2347


  11 in total

Review 1.  Recent advances in the molecular genetics of hypertrophic cardiomyopathy.

Authors:  A J Marian; R Roberts
Journal:  Circulation       Date:  1995-09-01       Impact factor: 29.690

2.  Cardiovascular anomalies associated with tetralogy of Fallot.

Authors:  G I Nagao; G I Daoud; A J McAdams; D C Schwartz; S Kaplan
Journal:  Am J Cardiol       Date:  1967-08       Impact factor: 2.778

3.  Congenital anomalies in the heart with hypertrophic cardiomyopathy.

Authors:  J Somerville; L McDonald
Journal:  Br Heart J       Date:  1968-09

4.  Short arm deletion of chromosome 1: del(1)(p13.3 p22.3) in a female infant with an extreme tetralogy of Fallot.

Authors:  H Tabata; K Sone; T Kobayashi; T Yanagisawa; T Tamura; N Shimizu; Y Kanbe; M Tashiro; S Ono; T Kuroume
Journal:  Clin Genet       Date:  1991-02       Impact factor: 4.438

5.  Tetralogy of Fallot, pulmonary valve stenosis, ventricular septal defect, and hypertrophic cardiomyopathy in WKY/NCrj rats.

Authors:  T Kuribayashi; K Shimoo; T Nakamura; H Taniwaki; K Hamaoka; M Nakagawa; Y Ibata; T Komeda; A Nagaoka
Journal:  Pediatr Res       Date:  1990-05       Impact factor: 3.756

6.  Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Authors:  L Thierfelder; H Watkins; C MacRae; R Lamas; W McKenna; H P Vosberg; J G Seidman; C E Seidman
Journal:  Cell       Date:  1994-06-03       Impact factor: 41.582

Review 7.  Tetralogy of Fallot with hypertrophic cardiomyopathy--an unknown combination.

Authors:  A S Rao; S K Gupta; K N Reddy; H S Somanath; B V Manjunath; J S Murthy; K A Abraham
Journal:  Indian Heart J       Date:  1989 Sep-Oct

Review 8.  San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease.

Authors:  B D Gelb; J A Towbin; E R McCabe; E Sujansky
Journal:  Am J Med Genet       Date:  1991-09-15

9.  Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.

Authors:  H Watkins; D Conner; L Thierfelder; J A Jarcho; C MacRae; W J McKenna; B J Maron; J G Seidman; C E Seidman
Journal:  Nat Genet       Date:  1995-12       Impact factor: 38.330

10.  Hypertrophic cardiomyopathy in infants: clinical features and natural history.

Authors:  B J Maron; A J Tajik; H D Ruttenberg; T P Graham; G F Atwood; B E Victorica; J T Lie; W C Roberts
Journal:  Circulation       Date:  1982-01       Impact factor: 29.690

View more
  4 in total

1.  Unusual association of hypertrophic cardiomyopathy with complete atrioventricular canal defect and Down syndrome.

Authors:  B W Eidem; C Jones; F Cetta
Journal:  Tex Heart Inst J       Date:  2000

2.  Unusual cardiac associations with Tetralogy of Fallot-a descriptive study.

Authors:  Vishal Changela; Colin John; Sunita Maheshwari
Journal:  Pediatr Cardiol       Date:  2010-04-20       Impact factor: 1.655

3.  Heart Failure in Tetralogy of Fallot due to Associated Hypertrophic Obstructive Cardiomyopathy: A Lesson to Learn.

Authors:  Ashwin Kodliwadmath; Yash Shrivastava; Bhanu Duggal; Dibbendhu Khanra; N Nanda
Journal:  J Cardiovasc Echogr       Date:  2021-05-21

4.  Combined obstructive hypertrophic cardiomyopathy and double outlet right ventricle in an infant with Down syndrome.

Authors:  Laxmi Ghimire; Ossama Tawffik; Valerie A Schroeder
Journal:  Am J Case Rep       Date:  2013-11-01
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.