This document summarizes several genetic disorders associated with meiosis including Turner syndrome, Down syndrome, Klinefelter syndrome, and Trisomy X. Turner syndrome affects females and causes underdeveloped ovaries and other sexual organs. Down syndrome is caused by an extra 21st chromosome and results in short stature and distinctive facial features. Klinefelter syndrome affects males and is caused by an extra X chromosome, leading to less developed sex organs and potential learning disabilities. Trisomy X also involves an extra X chromosome in females and can cause mild learning delays.
This document summarizes several genetic disorders associated with meiosis including Turner syndrome, Down syndrome, Klinefelter syndrome, and Trisomy X. Turner syndrome affects females and causes underdeveloped ovaries and other sexual organs. Down syndrome is caused by an extra 21st chromosome and results in short stature and distinctive facial features. Klinefelter syndrome affects males and is caused by an extra X chromosome, leading to less developed sex organs and potential learning disabilities. Trisomy X also involves an extra X chromosome in females and can cause mild learning delays.
This document summarizes several genetic disorders associated with meiosis including Turner syndrome, Down syndrome, Klinefelter syndrome, and Trisomy X. Turner syndrome affects females and causes underdeveloped ovaries and other sexual organs. Down syndrome is caused by an extra 21st chromosome and results in short stature and distinctive facial features. Klinefelter syndrome affects males and is caused by an extra X chromosome, leading to less developed sex organs and potential learning disabilities. Trisomy X also involves an extra X chromosome in females and can cause mild learning delays.
TURNER SYNDROME -underdeveloped ovaries, uterus, and oviducts -do not experience normal ovarian function -short, broad chest, webbed neck, and puffiness or swelling of hands and feet. -low posterior hairline DOWN SYNDROME -The most common disorder of trisomy is Down Syndrome wherein the 21st chromosome has three instead of two. - Short stature, round head, flat face, slanting eyes, stubby fingers, wide gap between the first and second toes, short neck, short arms, and short legs Klinefelter Syndrome (47, XXY) • It is a chromosomal abnormality affecting the physical and cognitive development of males. • Underdeveloped prostate gland and testes • Lack of facial and body hair, breast enlargement, unusual small penis • Males have big hands and feet, unusual long arms and legs. • Delayed speech and language development, learning disabilities. Klinefelter Syndrome • Some variants of Klinefelter have more than one extra chromosome in each cell such as in 48, XXXY or 49, XXXXY that are associated with severe form of abnormality. TRISOMY X (XXX) • The abnormal presence of an extra X chromosome is also known as Trisomy X syndrome, which affects 1/1000 in females. • Affected individuals usually have mild symptoms or none at all. • Delays and language- based learning disabilities