Absence of another cardiac or systemic disease capable of producing hypertrophy
DCM
Dilated heart with decreased systolic function
Final common pathway for diverse disease processes that lead to heart failure
IMAGING
General Features
Echocardiographic Findings
Imaging Recommendations
DIFFERENTIAL DIAGNOSIS
PATHOLOGY
General Features
CLINICAL ISSUES
Presentation
Demographics
Natural History & Prognosis
Treatment
DIAGNOSTIC CHECKLIST
Consider
Image Interpretation Pearls
Selected References
Zaban NB et al: Fetal echocardiography is useful for screening fetuses with a family history of cardiomyopathy. Pediatr Cardiol. 41(8):1766-72, 2020
Yamamoto H et al: Prediction of postnatal clinical course in primary congenital dilated cardiomyopathy. Pediatr Int. 61(12):1196-201, 2019
Ezon DS et al: Echocardiographic parameters and outcomes in primary fetal cardiomyopathy. J Ultrasound Med. 35(9):1949-55, 2016
Moon-Grady AJ: Fetal echocardiography in twin-twin transfusion syndrome. Am J Perinatol. 31 Suppl 1:S31-8, 2014
Weber R et al: Spectrum and outcome of primary cardiomyopathies diagnosed during fetal life. JACC Heart Fail. 2(4):403-11, 2014
Mongiovì M et al: Diagnosis and prognosis of fetal cardiomyopathies: a review. Curr Pharm Des. 16(26):2929-34, 2010
Yinon Y et al: Fetal cardiomyopathy--in utero evaluation and clinical significance. Prenat Diagn. 27(1):23-8, 2007
Barth PG et al: X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update. Am J Med Genet A. 126(4):349-54, 2004
Huhta JC: Guidelines for the evaluation of heart failure in the fetus with or without hydrops. Pediatr Cardiol. 25(3):274-86, 2004
Karatza AA et al: Isolated non-compaction of the ventricular myocardium: prenatal diagnosis and natural history. Ultrasound Obstet Gynecol. 21(1):75-80, 2003
Pedra SR et al: Fetal cardiomyopathies: pathogenic mechanisms, hemodynamic findings, and clinical outcome. Circulation. 106(5):585-91, 2002
Absence of another cardiac or systemic disease capable of producing hypertrophy
DCM
Dilated heart with decreased systolic function
Final common pathway for diverse disease processes that lead to heart failure
IMAGING
General Features
Echocardiographic Findings
Imaging Recommendations
DIFFERENTIAL DIAGNOSIS
PATHOLOGY
General Features
CLINICAL ISSUES
Presentation
Demographics
Natural History & Prognosis
Treatment
DIAGNOSTIC CHECKLIST
Consider
Image Interpretation Pearls
Selected References
Zaban NB et al: Fetal echocardiography is useful for screening fetuses with a family history of cardiomyopathy. Pediatr Cardiol. 41(8):1766-72, 2020
Yamamoto H et al: Prediction of postnatal clinical course in primary congenital dilated cardiomyopathy. Pediatr Int. 61(12):1196-201, 2019
Ezon DS et al: Echocardiographic parameters and outcomes in primary fetal cardiomyopathy. J Ultrasound Med. 35(9):1949-55, 2016
Moon-Grady AJ: Fetal echocardiography in twin-twin transfusion syndrome. Am J Perinatol. 31 Suppl 1:S31-8, 2014
Weber R et al: Spectrum and outcome of primary cardiomyopathies diagnosed during fetal life. JACC Heart Fail. 2(4):403-11, 2014
Mongiovì M et al: Diagnosis and prognosis of fetal cardiomyopathies: a review. Curr Pharm Des. 16(26):2929-34, 2010
Yinon Y et al: Fetal cardiomyopathy--in utero evaluation and clinical significance. Prenat Diagn. 27(1):23-8, 2007
Barth PG et al: X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update. Am J Med Genet A. 126(4):349-54, 2004
Huhta JC: Guidelines for the evaluation of heart failure in the fetus with or without hydrops. Pediatr Cardiol. 25(3):274-86, 2004
Karatza AA et al: Isolated non-compaction of the ventricular myocardium: prenatal diagnosis and natural history. Ultrasound Obstet Gynecol. 21(1):75-80, 2003
Pedra SR et al: Fetal cardiomyopathies: pathogenic mechanisms, hemodynamic findings, and clinical outcome. Circulation. 106(5):585-91, 2002
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