Let's see if the 2 psychos can come up with any "lies" I've posted. Lol.

I'm waiting.
Start with calling what isn't a birth defect a birth defect, what isn't a disease a disease, and what isn't a mutation a mutation.
They are birth defects, mutations, and diseases, and I posted links that prove it.

Shall I post them again?
Here . . .
People usually have 46 chromosomes in each cell. Two of the 46 chromosomes, known as X and Y, are called
sex chromosomes because they help determine whether a person will develop male or female sex characteristics. Girls and women typically have two X chromosomes (46,XX karyotype), while boys and men usually have one
X chromosome and one
Y chromosome (
46,XY karyotype). InSwyer syndrome, individuals with one X chromosome and one Y chromosome in each cell, the pattern typically found in boys and men, have
female reproductive structures.
People with Swyer syndrome have typical female external genitalia. The uterus and fallopian tubes are normally-formed, but the gonads (ovaries or testes) are not functional; affected individuals have undeveloped clumps of tissue called streak gonads. Because of the lack of development of the gonads, Swyer syndrome is also called 46,XY complete gonadal dysgenesis. The residual gonadal tissue often becomes cancerous, so it is usually removed surgically early in life.
People with Swyer syndrome are typically raised as girls and have a female gender identity. Because they do not have functional ovaries, affected individuals usually begin hormone replacement therapy during adolescence to induce menstruation and development of female secondary sex characteristics such as breast enlargement and uterine growth. Hormone replacement therapy also helps reduce the risk of reduced bone density (osteopenia and
osteoporosis). Women with this disorder do not produce eggs (ova), but they may be able to become pregnant with a donated egg or embryo.
Swyer syndrome usually affects only sexual development; such cases are called isolated Swyer syndrome. However, depending on the genetic cause, Swyer syndrome may also occur along with health conditions such as nerve problems (neuropathy) or as part of a syndrome such as
campomelic dysplasia, which causes severe skeletal abnormalities.
And. . .
Klinefelter's Syndrome / XXY Males: The Effects of Having an Extra Chromosome in Males
Klinefelter's Syndrome: the Effects of Having an Extra Chromosome
written by: Rafael•edited by:
Paul Arnold•updated: 9/10/2009
Genetic disorders come in a variety of forms. This article looks at how the possession of an extra chromosome produces a genetic disorder known as Klinefelter's syndrome.
- Klinefelter's syndrome, (also known as 47,XXY or XXY syndrome) is a genetic disorder in males caused by having an extra X chromosome instead of the usual XY pattern that men have. Klinefelter's syndrome is one of the most common chromosome abnormalities in humans since it has been estimated that 1 in 500 boys have it. The severity of the condition is variable. The main issue with Klinefelter's syndrome is male infertility but a variety of other symptoms may occur including problems with physical, language, and social development.
- What causes Klinefelter's syndrome?
Klinefelter's syndrome is a genetic disorder caused by a process known as “chromosome aneuploidy." Every cell in the human body has 23 pairs of chromosomes (for a total of 46). The 23rd pair of chromosomes are the sex chromosomes. Females typically have two X chromosomes, while males typically have one X chromosome and one Y chromosome.
Sometimes during cell division a non-correct disjunction of chromosomes may occur. This is where chromosomes fail to separate properly during meiosis, and in this case results in an extra copy of an X chromosome. When a gamete of this type is fertilised by a normal gamete, there will be an unequal number of chromosomes in all the resulting cells of the new individual.
- Symptoms of the XXY condition
In general, there is a delay in physical development in males who have the genetic abnormality. Normal physical milestones such as sitting, crawling, and walking are achieved at older ages in Klinefelter’s patients. Weak muscles and reduced strength are usually observed in babies and toddlers with the syndrome. They tend to be taller with less muscular development, less hair on face and body, and broader hips. Also they usually have less energy than regular boys. In adulthood, XXY males are taller and tend to develop health issues such as autoimmune disorders, breast cancer, vein diseases, osteoporosis, and tooth decay.Male infertility is the most common issue in males with Klinefelter's disease.
XXY males usually have language problems. They learn to speak late and have problems using language to express thoughts. Also, Klinefelter's males have a harder time at reading and writing assignments.