Early Identification of Severe Combined Immunodeficiency (SCID) Through Newborn Screening

Newborn Screening

Early Identification of Severe Combined Immunodeficiency (SCID) Through Newborn Screening Severe Combined Immunodeficiency (SCID) is a rare, life-threatening genetic disorder that severely impairs the immune system’s ability to protect the body from infections. SCID is often called bubble boy disease” due to its portrayal in popular culture. Infants born with SCID lack functional T cells…

Cystic Fibrosis- What if it is Left Undetected and clinical significance of Newborn Screening

Newborn Screening

Cystic Fibrosis- What if it is Left Undetected and clinical significance of Newborn Screening Cystic Fibrosis (CF) is a progressive, genetic (inherited) disorder primarily affecting the respiratory and digestive systems. While significant progress has been made in managing this condition, early detection remains crucial for ensuring better outcomes and improving the quality of life for…