WebKlinefelter syndrome (KS), also known as 47,XXY, is an aneuploid genetic condition where a male has an additional copy of the X chromosome. The primary features are infertility and small, poorly functioning testicles. Usually, symptoms are subtle and subjects do not realize they are affected. Sometimes, symptoms are more evident and may include weaker … WebDown syndrome is a relatively common birth defect, affecting about 1 in every 750 births. ... Other configurations of the sex chromosomes have been observed in 47,XXX females and 47,XYY males ...
Triple X Syndrome: What Is It, Causes, Diagnosis & Treatment
WebMay 16, 2024 · Down Syndrome. Down syndrome occurs as a result of maternal nondisjunction during meiosis I. It produces an egg cell with an extra copy of chromosome 21. ... (Klinefelter syndrome), or male with … WebXYY syndrome is a chromosomal condition which occurs only in males. A chromosome is a rod-like structure present in the nucleus of all body cells, with the exception of the red blood cells. Normally humans have 23 pairs of chromosomes, 46 chromosomes in total. The twenty-third pair are referred to as the sex chromosomes: a female has a XX pair ... porthole hardware
Y Chromosome Overview & Disorders What Does the Y …
WebSep 26, 2024 · Jacobs syndrome, also known as 47,XYY syndrome, is a rare genetic condition that occurs in about 1 out of 1000 male children. It belongs to a group of conditions known as "sex chromosome trisomies", with Klinefelter's syndrome being the more common type. [1] This condition was initially discovered in the 1960s. [2] Web47,XYY syndrome is associated with an increased risk of learning disabilities and delayed development of speech and language skills. Affected children can have delayed … WebAug 10, 2024 · It is suggested that XYY syndrome is not 100% a genetic disorder, nor it is inherited. Most cases are due to a random error occuring during the sexual reproduction process. Physical causes. In most cases, … optic goffin martignas