Category: Molecular Biology and Applied Genetics

Introduction  Cystic fibrosis (CF) is a hereditary, autosomal recessive disorder. It primarily affects the respiratory, digestive, and sweat gland systems. READ MORE ………….

Introduction Hermaphroditism refers to a group of congenital conditions in which an individual shows discordance between chromosomal sex, gonadal sex, READ MORE ………….

Introduction  Turner’s Syndrome is a genetic condition that affects only females. It occurs when one X chromosome is missing or READ MORE ………….

Introduction Klinefelter Syndrome (KS) is a chromosomal disorder affecting males, caused by the presence of one or more extra X READ MORE ………….

Introduction DiGeorge Syndrome (DGS) is a genetic disorder caused by a deletion on chromosome 22 (22q11.2 deletion). It affects the READ MORE ………….