Triple X syndrome presents itself as an abnormality of the chromosomes in a female’s body. Normal females have two X chromosomes, one contributed by each parent. Patients with triple X syndrome have three X chromosomes. Healthy people have 46 chromosomes per cell in their bodies. Of these, two known as X and Y, are called sex chromosomes because their genetic codes determine whether a person will be male or female. Females normally have two X chromosomes and males have one X chromosome and one Y chromosome. Triple X syndrome occurs when an extra X chromosome is present in each of the female’s cells. This results in the female having 47 chromosomes instead of the normal 46.
Many girls grow into adulthood without knowing they have triple X syndrome because the symptoms are often vague. Some females grow taller than average, but the condition doesn’t normally jordan 3 cause abnormal physical features. The majority of women with triple X syndrome experience normal sexual development and can conceive children.
Triple X syndrome has been associated with a higher rate of learning disabilities and slow development of language and speech skills. Also observed has been slow manifestation of motor skills, such as walking and sitting and lack of muscle tone. Triple X syndrome females are often slightly lower in intelligence than females without the condition. jordan 12 Some functional and emotional impairment are also possible, but these traits vary dramatically among affected females. Acting in a cascading effect, slower learning abilities or delayed development could ultimately lead to other issues, such as academic problems and underdeveloped socialization skills, potentially causing social isolation.
Triple X syndrome is generally considered a non inherited condition. The chromosomal abnormality often occurs as a random event when the egg and sperm join to form the reproductive cell. An aberrant number of chromosomes in a reproductive cell occurs as a result of an error in cell division called nondisjunction. An egg or sperm cell can acquire an extra X chromosome because of nondisjunction. If one of these cells becomes a contributor to the genetic makeup of a fetus, the resulting child will carry an extra X chromosome in each of her body’s cells.
How to Diagnose Triple X Syndrome
Occurring when an extra X chromosome is attached to each cell in a jordan 7 female body, Triple X syndrome affects approximately 0.1 percent.
Triple A Symptoms
Triple A Symptoms. Triple A stands for abdominal aortic aneurysm. The abdominal aorta is a large blood vessel that supplies blood to.
People With Triple X Syndrome
Triple X syndrome, also known as trisomy X, is a genetic disorder in which a female carries an extra copy of the.
About Triple X Syndrome
Triple X syndrome is a chromosomal abnormality that affects about one in 1,000 females. While girls normally are born with two X.
How to Help a Child Grow Taller
A child maximum height is typically determined by genetics. Reaching maximum height is determined by multiple factors, including general health and hormones.
Triple X Syndrome Characteristics
Triple X Syndrome Characteristics. Those afflicted by the genetic disorder called Triple X syndrome have an extra X chromosome inside each of.
How to Treat Chromosomal Abnormalities
Chromosomal abnormalities have both a genetic and environmental risk factor. While abnormalities are often hereditary traits, certain environmental factors are known .