Simplifying Allied Health Learning.
Introduction Hermaphroditism refers to a group of congenital conditions in which an individual shows discordance between chromosomal sex, gonadal sex, and phenotypic (external genital) sex. In simple words: Sex development Read More ……..
Introduction Turner’s Syndrome is a genetic condition that affects only females. It occurs when one X chromosome is missing or partially missing. This chromosomal abnormality affects growth, puberty, fertility, and Read More ……..
Introduction Klinefelter Syndrome (KS) is a chromosomal disorder affecting males, caused by the presence of one or more extra X chromosomes in their cells — the most common form being Read More ……..
Introduction DiGeorge Syndrome (DGS) is a genetic disorder caused by a deletion on chromosome 22 (22q11.2 deletion). It affects the development of the thymus, parathyroid glands, and heart, leading to Read More ……..
Introduction Down Syndrome (Trisomy 21) is a genetic disorder caused by having an extra copy of chromosome 21. Normally, every person has 46 chromosomes (23 pairs). In Down’s Syndrome, there Read More ……..