[HTML][HTML] Left ventricular noncompaction− Risk stratification and genetic consideration−
F Ichida - Journal of Cardiology, 2020 - Elsevier
Left ventricular noncompaction (LVNC) is a cardiomyopathy characterized by two layered
structures composed of prominent trabecular meshwork and deep intertrabecular recesses …
structures composed of prominent trabecular meshwork and deep intertrabecular recesses …
Genetic contribution to congenital heart disease (CHD)
NA Shabana, SU Shahid, U Irfan - Pediatric cardiology, 2020 - Springer
Congenital heart defects (CHD) are the most common congenital problems in neonates. The
basis for CHD is multifactorial, involving genetic and environmental components. The …
basis for CHD is multifactorial, involving genetic and environmental components. The …
Genetic basis of human congenital heart disease
SN Nees, WK Chung - Cold Spring Harbor perspectives …, 2020 - cshperspectives.cshlp.org
Congenital heart disease (CHD) is the most common major congenital anomaly with an
incidence of∼ 1% of live births and is a significant cause of birth defect–related mortality …
incidence of∼ 1% of live births and is a significant cause of birth defect–related mortality …
[HTML][HTML] Genetic and genomics in congenital heart disease: a clinical review
A Saliba, ACV Figueiredo, JE Baroneza, JY Afiune… - Jornal de …, 2020 - SciELO Brasil
Objective: Discuss evidence referring to the genetic role in congenital heart diseases,
whether chromosomic alterations or monogenic diseases. Data source: LILACS, PubMed …
whether chromosomic alterations or monogenic diseases. Data source: LILACS, PubMed …
The genetics of isolated congenital heart disease
SN Nees, WK Chung - … Journal of Medical Genetics Part C …, 2020 - Wiley Online Library
The genetic mechanisms underlying congenital heart disease (CHD) are complex and
remain incompletely understood. The majority of patients with CHD have an isolated heart …
remain incompletely understood. The majority of patients with CHD have an isolated heart …
[HTML][HTML] Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways
E Suluba, L Shuwei, Q Xia, A Mwanga - Egyptian Journal of Medical …, 2020 - Springer
Abstract Background Congenital heart diseases (CHDs) are the most common congenital
anomalies with an estimated prevalence of 8 in 1000 live births. CHDs occur as a result of …
anomalies with an estimated prevalence of 8 in 1000 live births. CHDs occur as a result of …
Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart
E Auxerre-Plantié, T Nielsen… - Disease models & …, 2020 - journals.biologists.com
The causal genetic underpinnings of congenital heart diseases, which are often complex
and multigenic, are still far from understood. Moreover, there are also predominantly …
and multigenic, are still far from understood. Moreover, there are also predominantly …
Novel KLHL26 variant associated with a familial case of Ebstein's anomaly and left ventricular noncompaction
SSK Samudrala, LM North, KD Stamm… - … Genetics & Genomic …, 2020 - Wiley Online Library
Background Ebstein's anomaly (EA) is a rare congenital heart disease of the tricuspid valve
and right ventricle. Patients with EA often manifest with left ventricular noncompaction …
and right ventricle. Patients with EA often manifest with left ventricular noncompaction …
[HTML][HTML] Genetics of inherited cardiomyopathies in Africa
G Shaboodien, TF Spracklen, S Kamuli… - Cardiovascular …, 2020 - ncbi.nlm.nih.gov
Abstract In sub-Saharan Africa (SSA), the burden of noncommunicable diseases (NCDs) is
rising disproportionately in comparison to the rest of the world, affecting urban, semi-urban …
rising disproportionately in comparison to the rest of the world, affecting urban, semi-urban …
[HTML][HTML] Genética e genômica na cardiopatia congênita: uma revisão clínica
A Saliba, ACV Figueiredo, JE Baroneza, JY Afiune… - Jornal de …, 2020 - SciELO Brasil
Objective: Discuss evidence referring to the genetic role in congenital heart diseases,
whether chromosomic alterations or monogenic diseases. Data source: LILACS, PubMed …
whether chromosomic alterations or monogenic diseases. Data source: LILACS, PubMed …