Chromosomale afwijking xxy
Chromosomale afwijking
Chromosomale afwijking xxy | These symptoms are often noticed only at puberty, although this is one of the most common chromosomal disorders , occurring in one to two per 1, live births. |
Klinefelter syndrome | Het syndroom van Klinefelter [ 3 ] is een genetische aandoening bij de man waarbij hij in zijn cellen ten minste een X-chromosoom te veel heeft. |
Chromosomale afwijking baby | Back to Health A to Z. |
Klinefelter syndrome - NHS | . |
Chromosomale afwijkingen lijst
- Syndroom van Klinefelter - Wikipedia Klinefelter syndrome, also known as XXY syndrome, is a condition in boys and men that’s caused by an extra X chromosome. It can affect physical and mental development.
- Klinefelter syndrome - Wikipedia Rather than the usual pattern of 46 chromosomes, with one X chromosome and one Y chromosome, there is an additional X chromosome, resulting in a genetic signature of 47,XXY.
- Males with a normal male karyotype (XY) in some cells may be fertile and have less obvious malformations. Some affected men have 3, 4, and even 5 X chromosomes along with the Y. .
- Symptoms of Klinefelter syndrome XXY occurs when a male has an extra X chromosome in some or all cells of his body. About 1 out of every males is born with XXY, and there about , with this condition in the U.S. .