- 06 May 2019 02:20
#15002987
It constituted family violence because the father talked to conservative media outlets, thus exposing his child to significant harm. Probably this girl is a XY female with Swyer syndrome. In Swyer syndrome, individuals with a X chromosome and a Y chromosome, which are typically found in boys and men, have female external genitalia. If the girl is formally diagnosed with Swyer syndrome after a genetic test, it would be much easier for the father to accept her.
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A messy legal dispute between a 14-year-old transgender boy and his father, who rejects the child’s gender identity, has expanded into a fight over freedom of expression.
In a recent decision, a B.C. Supreme Court judge ordered the father to stop publicly discussing the case after finding some of his actions, including interviews with conservative media outlets, exposed his child to significant harm and constituted “family violence.”
https://nationalpost.com/news/canada/le ... expression
It constituted family violence because the father talked to conservative media outlets, thus exposing his child to significant harm. Probably this girl is a XY female with Swyer syndrome. In Swyer syndrome, individuals with a X chromosome and a Y chromosome, which are typically found in boys and men, have female external genitalia. If the girl is formally diagnosed with Swyer syndrome after a genetic test, it would be much easier for the father to accept her.
Swyer syndrome is a condition that affects sexual development. Sexual development is usually determined by an individual's chromosomes; however, in Swyer syndrome, sexual development does not match the affected individual's chromosomal makeup.
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). In Swyer 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.
https://ghr.nlm.nih.gov/condition/swyer-syndrome
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