The newborn hearing screening test is designed to detect permanent hearing loss in babies at the earliest stage. By identifying hearing issues soon after birth, parents can take timely action and get the right support, guidance, and treatment options from healthcare professionals. Early detection plays a vital role in helping babies develop proper speech, language, and communication skills, ensuring they get the best possible start in life.
Early Detection: Identifies hearing loss right after birth, avoiding delays in diagnosis.
Timely Intervention: Allows parents to start treatment or therapies early for better results.
Improved Development: Supports healthy speech, language, and cognitive development.
Parental Support: Provides families with expert guidance, counseling, and resources.
Better Quality of Life: Helps the child adapt and thrive with early care and support.
Genetic Factors: Some babies inherit hearing loss from their parents, even if the parents don’t have symptoms.
Premature Birth: Babies born before full term have a higher risk of hearing problems.
Infections During Pregnancy: Conditions like rubella, cytomegalovirus (CMV), or toxoplasmosis can affect the baby’s hearing.
Birth Complications: Lack of oxygen at birth or very low birth weight can harm the hearing system.
Jaundice (Severe Cases): High bilirubin levels can sometimes damage the hearing nerve.
Certain Medications: Some antibiotics or treatments given to the mother or baby may affect hearing.
Noise Exposure or Trauma: Though rare in newborns, loud noises or injuries can also impact hearing.