If you have just found out through prenatal testing that your baby has or may have Jacobs syndrome 47,XYY, and are looking for more information, the Genetic Support Foundation is a good starting point.
There are many other important resources out there, including your doctor and genetic counselor. We have also compiled a list of resources that can provide you with additional information and support. After reviewing the information below, if you have a question that you are having difficulty finding an answer for, please feel free to contact us.
Each individual with Jacob’s syndrome is unique. Some individuals with Jacob’s syndrome may be above average height, but Jacob’s syndrome does not affect other physical features. Sexual development is also normal. Individuals with Jacob’s syndrome have an increased risk of learning disabilities, delayed speech, and behavioral problems. A small number of those with Jacob’s syndrome are also diagnosed with autism spectrum disorders. The symptoms of Jacob’s syndrome vary greatly from person to person, but they are generally mild and some individuals with Jacob’s syndrome may remain undiagnosed.
People with Jacob’s syndrome can have loving relationships with friends and family, go to school with their peers, and develop their social skills and communication. Individuals with Jacob’s syndrome live healthy, full, and independent lives. Most men with Jacob’s syndrome are able to have children of their own.
In a typical genome, individuals have two sex chromosomes to determine biological sex. Women usually have two X chromosomes (one from mom and one from dad), and men usually have one X chromosome (from mom) and one Y chromosome (from dad). Individuals with Jacob’s syndrome have one X chromosome and two Y chromosomes, so they have 47 chromosomes total and their sex chromosomes are XYY. Jacob’s syndrome is usually caused by a cell division error in the sperm before conception. Rarely, the cell division error may occur after conception. These individuals may have mosaic Jacob’s syndrome, meaning some of their cells are XYY and some are XY.
Jacob’s syndrome is associated with few health or developmental concerns.
Increased height is one of the main symptoms of Jacob’s syndrome and may be noticeable as early as 5 years old. Jacob’s syndrome does not cause infertility or abnormal sexual development. Speech delays and learning disabilities such as dyslexia occur in some individuals with Jacob’s syndrome. Some individuals with Jacob’s syndrome may also develop behavioral issues. There is a small increased risk of autism spectrum disorders associated with Jacob’s syndrome.
Most cases of Jacob’s syndrome are not inherited, but are caused by a cell division error in the sperm before conception. Mosaic Jacob’s syndrome is also not inherited. The chance of having another baby with Jacob’s syndrome does not increase in these cases.
There is no “cure” for Jacob’s syndrome, but therapeutic intervention can help individuals struggling with learning disabilities or behavioral issues reach their full potential. Speech therapy can be beneficial to individuals with speech delays. School support for learning disabilities and/or educational therapy can also be beneficial. Individuals with Jacob’s syndrome tend to respond well to intervention measures, and in some individuals these issues may resolve completely.
It is important to recognize that the health and developmental effects of Jacob’s syndrome vary from person to person. Therapy and other interventions such as speech therapy and support for learning disabilities can be beneficial to individuals with Jacob’s syndrome. Men with Jacob’s syndrome are expected to live full, independent lives
Jacob’s syndrome is estimated to occur in 1 in 1,000 newborn boys.
The Association for X and Y Variations (AXYS) is an advocacy, education and support organization for individuals with X and Y chromosome variations and their families.
AXYS is a nonprofit 501(c)(3) organization formed by the merger of KS&A (formerly Klinefelter Syndrome and Associates) and AAKSIS (American Association for Klinefelter Syndrome Information and Support). The XXYY Project maintains separate 501(c)(3) status but partners with AXYS on programs, administration, advocacy and support efforts.
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