Webhits early to Jan The graph below shows the number of accesses hits per month to the contents list, general pages, and graphics on the site. Up to January the figures were provided by medhelp. The numbers started off lower than those provided by medhelp. African medal-winning runner accused of not being a woman and AIS was mentioned quite a lot in the media.
This topic is continued from the previous essay. This section of the ReligiousTolerance. Most transgender people were identified by physicians as male at birth, and recorded as male on their birth certificate. However, often as children from 3 to 5 years-of-age, they will personally identify as female.
Many will say that they have female brain trapped in a male body. A large minority of transgender people were identified as female at birth, were observed as having "lady parts," but now identify as male.
Small percentages of transgender persons will identify themselves as both male and female, or neither male nor female gender. People with CAIS have many similarities to transgender persons.
CAIS causes them to appear female at birth, be identified as female Androgen insensitivity syndrome ais essay their birth certificate, and self-identify as female during their childhood. They are typically raised as girls by their parents.
However, later in life, a medical concern will usually surface. Their menstruation cycles may not begin as expected, or they may find it impossible to become pregnant.
About one in three persons with CAIS do not develop armpit hair. A doctor may order a DNA test and find that the patient's sex chromosomes are not the expected XX female pattern. Their chromosomes are XY, or some other pattern that contains a Y chromosome.
That is, the person is a genetic or biological male! Needless to say, this is a very difficult finding for a physician to communicate to their patient. It almost always will be a serious shock to the patient with CAIS.
It takes time for them to accept and understand their situation. People with CAIS are not considered to be transgender.
However, we will describe it here because the syndrome creates an emotional conflict that is very similar to being transgender. People with CAIS don't usually go through a gender identity transition after they find out that they are genetic males.
They continue their female gender identity, gender presentation, and female appearance, after their diagnosis. The presence of one or rarely more than one "Y" chromosome in an individual's DNA indicates that their biological sex is male.
This causes their body's cells to be unable to respond to androgens. The result is that these biological males typically look female, act female, have a female body, are brought up as female, and identify themselves as female throughout their life.
Their main deviations from a "standard" female body is that they have no uterus, ovaries or fallopian tubes. However, they do have a pair of undescended testicles in their body. These are internal organs and thus are not obvious at birth. Thus, a person with CAIS is usually assumed to be female, are registered as such on their birth certificate, and raised as a girl.
Their genitals appear female. That is because the genitals of all embryos start off as female. It is only when embryos with male sex chromosomes in their DNA start producing testosterone that the embryo normally begins to develop male genital structures. Since genetic males who have CAIS cannot respond to male hormones, they continue developing with a female body.
Usually, none of the medical professionals attending their birth will suspect that the newborn is a genetic male. Babies with CAIS are generally raised as girls. As they go through puberty, female secondary sexual characteristics, including breasts, lack of an Adam's Apple laryngeal prominenceetc.
Often, the first indication of CAIS occurs when their periods do not start when expected. They might go to a doctor, have their DNA checked, and be totally shocked to find out that they are biologically male.
During the yeara small scale study of 20 children and 10 adult women with CAIS found that: Emotional reactions were more long-lasting in mothers and adult patients than in fathers.hora May 18, at Tigger, I think there is indeed a strain within trans sctivism (and, more generally, gay male culture as epitomized by drag) that truly does hate women so much that they feel driven to re-make what womanhood IS.
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Androgen Insensitivity Syndrome, Androgen Resistance Syndrome, Testicular Feminization Syndrome (Testicular Feminisation Syndrome), Feminizing Testes Syndrome (Feminising Testes Syndrome), Male Pseudo-hermaphroditism, Morris’s Syndrome (CAIS), Goldberg-Maxwell Syndrome, Reifenstein Syndrome (PAIS), Gilbert-Dreyfus Syndrome (PAIS), Rosewater Syndrome (PAIS), Lubs Syndrome . Androgen insensitivity syndrome (AIS) is a congenital disorder in which a defect in the androgen receptor (AR) gene leads to cellular resistance to androgens. Defects in the AR gene, located on the X chromosome, result in the development of a feminine phenotype in . Androgen insensitivity syndrome (AIS) is an intersex condition that results in the partial or complete inability of the cell to respond to androgens.
Psychogeography essay Psychogeography essay wolfgang stossel yunusemremert.comophy essay on death altazor o el viaje en paracaidas analysis essay the fall of france essay dissertation agregation histoire geographie. Overview of people with Complete Androgen Insensitivity Syndrome (CAIS): This section of the yunusemremert.com web site deals with transgender persons.
Most transgender people were identified by physicians as male at birth, and recorded as male on their birth certificate. Androgen insensitivity syndrome (AIS) is typically characterized by evidence of feminization (i.e., undermasculinization) of the external genitalia at birth, abnormal secondary sexual development in puberty, and infertility in individuals with a 46,XY karyotype.
Androgen Insensitivity Syndrome, Androgen Resistance Syndrome, Testicular Feminization Syndrome (Testicular Feminisation Syndrome), Feminizing Testes Syndrome (Feminising Testes Syndrome), Male Pseudo-hermaphroditism, Morris’s Syndrome (CAIS), Goldberg-Maxwell Syndrome, Reifenstein Syndrome (PAIS), Gilbert-Dreyfus Syndrome (PAIS), Rosewater Syndrome (PAIS), Lubs Syndrome .
Androgen insensitivity syndrome (AIS) is a congenital disorder in which a defect in the androgen receptor (AR) gene leads to cellular resistance to androgens. Defects in the AR gene, located on the X chromosome, result in the development of a feminine phenotype in .