Results 41 to 50 of about 2,884 (194)

The Left Ventricular Myocardium in Hypoplastic Left Heart Syndrome

open access: yesJournal of Cardiovascular Development and Disease, 2022
Hypoplastic left heart syndrome (HLHS) is a collective term applied to severe congenital cardiac malformations, characterised by a combination of abnormalities mainly affecting the left ventricle, associated valves, and ascending aorta.
Bill Chaudhry   +6 more
doaj   +1 more source

Endocardial Fibrosis Elastosis [PDF]

open access: yesJACC: Basic to Translational Science
Marlin Touma, MD, PhD
doaj   +2 more sources

Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11 [PDF]

open access: yes, 2016
Variants in NDUFB11, which encodes a structural component of complex I of the mitochondrial respiratory chain (MRC), were recently independently reported to cause histiocytoid cardiomyopathy (histiocytoid CM) and microphthalmia with linear skin defects ...
Ashworth, M   +19 more
core   +1 more source

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) presenting with ventricular fibrillation in an adult: a case report [PDF]

open access: yes, 2008
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly. The usual clinical course is severe left sided heart failure and mitral valve insufficiency presenting during the first months of life. However,
Thomas Kristensen   +19 more
core   +1 more source

MUMPS MYOCARDITIS AS A CAUSE OF NEONATAL CARDIOGENIC SHOCK [PDF]

open access: yesActa Medica Iranica, 2008
The mothers may be infected during pregnancy with infectious agents. Mumps induced myocarditis, especially endocardial fibroelastosis, was previously a common disease of infants but is rare now.
M. Kadivar   +3 more
doaj   +1 more source

Three de novo variants in KMT2A (MLL) identified by whole exome sequencing in patients with Wiedemann–Steiner syndrome

open access: yesMolecular Genetics & Genomic Medicine, 2021
Background Wiedemann–Steiner syndrome (WSS) is an autosomal dominant disorder characterized by short stature, hypertrichosis, intellectual disability, developmental delay, along with facial dysmorphism.
Sukun Luo   +8 more
doaj   +1 more source

Niewyjaśniona niewydolność serca u 14-miesięcznego dziecka [PDF]

open access: yes, 2019
Endocardial fibroelastosis is a cardiomyopathy rarely seen in the present age. Here, we report a case of 14-months-old baby who presented with failure to thrive, sweating while feeding, a dilated left ventricle, and left ventricular dysfunction.
Abhishekh, Nishant Kumar   +4 more
core   +2 more sources

MR findings of endocardial fibroelastosis in children [PDF]

open access: yes, 2008
BACKGROUND: Endocardial fibroelastosis (EFE) is characterized by a diffuse white fibrous tissue lining the endocardium. The diagnosis is difficult to establish because clinical symptoms and electrocardiographic findings are nonspecific.
Ensing, Gregory J   +2 more
core   +1 more source

Eosinophilic myocarditis mimicking acute coronary syndrome secondary to idiopathic hypereosinophilic syndrome: a case report [PDF]

open access: yes, 2010
Introduction Eosinophilic myocarditis is a rare form of myocarditis. It is characterized pathologically by diffuse or focal myocardial inflammation with eosinophilic infiltration, often in association with peripheral blood eosinophilia.
Reza Amini   +21 more
core   +2 more sources

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