Which Neonatal Disorders Have a Strong Genetic Component?
Certain neonatal disorders have a strong genetic component and can be traced through family history. These include:
- Congenital Heart Defects: Often linked to genetic mutations or syndromes like Down syndrome. - Metabolic Disorders: Conditions like Phenylketonuria (PKU) and Galactosemia are inherited and can be detected through newborn screening. - Cystic Fibrosis: A common genetic disorder affecting the lungs and digestive system. - Muscular Dystrophy: A group of genetic disorders leading to muscle weakness and degeneration.
