Achondroplasia is the most common skeletal dysplasia found in humans, accounting for 90% of cases of disproportionate sh ...

Hemorrhagic disease of the newborn is a life-threatening condition that is due to insufficient vitamin K levels in newbo ...

Williams syndrome is a rare genetic disorder with congenital heart disease, distinctive facial features (elfin-like face ...

Umbilical arterial catheterization provides direct access to the arterial system, thus enabling arterial blood sampling ...

Morgagni hernias are rare congenital diaphragmatic defects that can lead to bowel obstruction and incarceration if not r ...

Zellweger syndrome, also known as cerebrohepatorenal syndrome, is a rare inherited disorder characterized by the absence ...