Short Description

The aim of newborn screening is to detect diagnostic markers of treatable disorders in blood spots collected from pre-symptomatic newborns. Early identification of disorders significantly improves long term prognosis of affected patients, minimizes complications, avoids unnecessary diagnostic testing and identifies families for whom pre-natal genetic counselling may be helpful.

PreTest Information

Clinical details and drug history must accompany sample.

Detail Description

Newborn Screening Panel Comprehensive Test

As a new parent, you want to do everything possible to ensure the health and wellbeing of your newborn. One important step in this process is to have your baby undergo a comprehensive newborn screening panel test. This test can help detect any genetic disorders or other health issues early on, which can be critical for effective treatment and management.

What is a Newborn Screening Panel Comprehensive Test?

A newborn screening panel comprehensive test is a blood test that screens for a variety of genetic disorders that may not be apparent at birth. These disorders can cause serious health problems if not detected and treated early on. The test is typically performed within 48-72 hours after birth, while the baby is still in the hospital.

What does the Newborn Screening Panel Comprehensive Test Screen For?

The newborn screening panel comprehensive test screens for a variety of genetic disorders, including:

• Phenylketonuria (PKU)
• Cystic Fibrosis
• Sickle Cell Disease
• Galactosemia
• Hypothyroidism
• Maple Syrup Urine Disease
• Biotinidase Deficiency
• Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD)
• And more

What are the Symptoms of these Disorders?

The symptoms of these disorders can vary widely depending on the specific disorder. Some common symptoms include:

• Fever
• Poor feeding
• Irritability
• Jaundice
• Failure to thrive
• Seizures
• And more

How is the Diagnosis Made?

The diagnosis is made through a blood test that is analyzed in a laboratory. If the test comes back positive for a specific disorder, further testing may be necessary to confirm the diagnosis. Early diagnosis and treatment is critical for the management of these disorders.

What is the Cost of the Newborn Screening Panel Comprehensive Test?

The cost of the newborn screening panel comprehensive test in India is typically around INR 7500. However, the cost can vary depending on the specific laboratory and location.

Why is the Newborn Screening Panel Comprehensive Test Important?

The newborn screening panel comprehensive test is important because it can help detect genetic disorders early on, before symptoms appear. Early diagnosis and treatment can prevent serious health problems and improve the long-term health outcomes for your baby.

At DNA Labs India, we offer comprehensive newborn screening panel tests to help ensure the health and wellbeing of your newborn. Our tests are performed in state-of-the-art laboratories and are designed to provide accurate and reliable results. Contact us today to learn more about our testing services.

Remember, early detection is the key to effective treatment and management of genetic disorders. Don't wait – schedule your newborn screening panel comprehensive test today!

The aim of newborn screening is to detect diagnostic markers of treatable disorders in blood spots collected from pre-symptomatic newborns. Early identification of disorders significantly improves long term prognosis of affected patients, minimizes complications, avoids unnecessary diagnostic testing and identifies families for whom pre-natal genetic counselling may be helpful.