I would go to chargesyndrome.org website. Contact someone there and they can give you the information you are wanting.
Charge syndrome is genetic. Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. This syndrome is a common cause of congenital anomalies affecting several tissues in nonrandom fashion. Some research has been shown that detected mutations are in the gene CHD7 in 10 of 17 individuals with CHARGE syndrome that didn't have microdeletions, accounting for the disease in most affected individuals.
An individual with Klinefelter syndrome is male. They are born with at least one extra X chromosome (XXY), which can affect their physical and cognitive development.
Oculo-Auriculo Vertebral Syndrome-is rere congenital defect characterised by incomplete development of ear ,nose,soft palte & mandibles
On the Charge Syndrome website, is a page that speaks about a charity that funds and takes care of families with children that have CHARGE syndrome and information about how it does so, and for what reasons.
i hope you die
people
No.
Chromosomal abnormalities can lead to intellectual disabilities, learning delays, and developmental disorders that may impact cognitive development. Conditions like Down syndrome, Turner syndrome, and Klinefelter syndrome are examples of chromosomal abnormalities that can affect cognitive functioning in different ways, depending on the specific genetic changes involved. Early intervention and individualized support can help mitigate these challenges and optimize cognitive development.
Prune belly syndrome is more common in males because the condition is thought to be linked to abnormalities in the development of male reproductive organs during fetal development. Specifically, the lack of abdominal wall muscles in prune belly syndrome is thought to be associated with developmental issues in male genitalia.
No. Asperger's Syndrome doesn't discriminate - ANYONE can have it.
Ribosomes
Triple X syndrome affects females and is caused by the presence of an extra X chromosome. This genetic condition can lead to mild to moderate intellectual and developmental delays, as well as tall stature and some physical differences. It may also affect reproductive system development and function.