Professional cardiology societies have issued an updated guideline for the management of adult patients with congenital heart ...

Congenital heart disease (CHD) is one of the most common birth defects, but the full extent of its genetic underpinnings has been a mystery. Now, a new study of more than 11,000 children with CHD ...

Congenital fibrinogen disorders encompass a heterogeneous group of inherited conditions affecting either the quantity or quality of fibrinogen, a critical glycoprotein in the coagulation cascade.

Congenital ichthyosis disorders constitute a complex, genetically heterogeneous group of hereditary skin conditions marked by aberrant epidermal differentiation and impaired barrier function. These ...

Centrosomes are small structures in cells with many essential functions, including roles in cell signaling and in organizing a cell’s cytoskeleton. Centrosome dysfunction contributes to diseases like ...

Children with neurodevelopmental disorders report congenital abnormalities, such as defects of the heart and/or urinary tract, at least ten times more frequent compared to other children. This is one ...

The research uncovers a novel variant in the MYO1D gene that is linked to laterality defects, congenital heart diseases, and sperm defects in humans. Laterality defects involve the abnormal ...

Jaipur: To spot congenital heart diseases (CHD) early, manage them, treat them, and keep up regular follow-ups, the health ...

Congenital factor VII deficiency is a rare, autosomal recessive disorder with an estimated prevalence of 1 in 1,000,000. We ...

STRING analysis of 60 significant genes in CHD. Genes not previously implicated in human CHD that have at least one edge are denoted by red star. Congenital heart disease (CHD) is one of the most ...