also known as non-cyanotic heart defect, is a class of congenital heart defects. In these, blood is shunted (flows) from the left side of the heart to the right side of the heart due to a structural defect (hole) in the interventricular septum
the ability to distinguish two points as separate structures rather a single fuzzy dot.
also called Heart and Hand Syndrome, atrio-digital syndrome, atriodigital dysplasia, cardiac-limb syndrome, heart-hand syndrome type 1, HOS, ventriculo-radial syndrome) is an autosomal dominant disorder that affects bones in the arms and hands (the upper limbs) and may also cause heart problems.
a birth defect of the abdominal (belly) wall. The baby's intestines are found outside of the baby's body, exiting through a hole beside the belly button.
The lowest point. The nadir may refer, for example, to the lowest blood count after chemotherapy or the lowest concentration of a drug in the body.
relating to the atrial and ventricular chambers of the heart, or the connection or coordination between them.
the spatial relationship between the ventricles and the primary arteries of the heart.
the enlargement of an organ or tissue from the increase in size of its cells
is an instrument that measures magnetism
is a type of cephalic disorder wherein the brain is located outside of the skull. This condition is usually found in embryos as an early stage of anencephaly.
is underdevelopment or incomplete development of a tissue or organ
a disorder that involves unusual facial characteristics, short stature, heart defects present at birth, bleeding problems, developmental delays, and malformations of the bones of the rib cage. Noonan syndrome is caused by changes in one of several autosomal dominant genes.
also known as 22q11.2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22. While the symptoms can be variable they often include congenital heart problems, specific facial features, frequent infections, developmental delay, learning problems, and cleft palate