MstrssPassion
Posts: 2444
Joined: 1/1/2004 From: West Palm Beach, FL Status: offline
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The following comes from several sources... The presence of one or two additional X chromosomes in a male (XXY or XXXY) may cause Klinefelter's syndrome. A single X chromosome (XO) is called Turner's syndrome. Is characterized by a lack or incomplete development of certain primary and secondary female characteristics and is associated with a range of medical issues. sex chromosomal mosaicism can cause what was once called "true hermaphroditism", the presence of both testicular and ovarian tissue in one individual One of the most common cases is a fetus with XY chromosomes but where for some reason a fertile male child does not develop. In the following cases the child retains an outward male appearance: Swyer syndrome - damaged testis-determining factor on their Y chromosome. Persistent mullerian duct syndrome: Child has internal uterus and fallopian tubes because Y chromosome fails to produce Mullerian inhibiting factor. The following further XY cases leads to intersexuality: Androgen insensitivity syndrome. They develop either partially or fully as females, due to their bodies failing to respond to testosterone. In the case of complete androgen insensitivity syndrome (CAIS), their tissues are totally insensitive to androgens, and they will develop as females, with normal female external organs. However, they will not develop a uterus or fallopian tubes, due to the production of Mullerian inhibiting factor by their testes. At puberty breasts will develop due to the production of estrogen by the testes; but no menstruation will occur due to the lack of a uterus. The tissues of individuals with partial androgen insensitivity, by contrast, have partial sensitivity to testosterone, but it is reduced compared to the male normal. These individuals can develop with either male external anatomy, or female external anatomy, or some combination, depending on the degree of insensitivity. 5-alpha-reductase deficiency. In this condition, individuals have testes, as well as vagina and labia, but with a small penis capable of ejaculation instead of a clitoris (this penis, however, appears to be a clitoris at birth). These individuals are normally raised as girls. However, come puberty, their testes will descend, their voice will deepen and they often will develop a male sexual identity. But they develop only limited facial hair. The number of people with this condition varies geographically, depending on how much of a given population is interrelated. Excessive in utero exposure to androgens may lead to intersexuality in XX cases: Congenital adrenal hyperplasia: Female internal anatomy, but ambiguous or male external genitalia, and develop male secondary sexual characteristics. Progestin-induced virilisation. In this case, the male hormones are caused by use of progestin, a drug that was used in the 1950s and 1960s in order to prevent miscarriage. These individuals have internal and external female anatomy. They develop however some male secondary characteristics, and they frequently have unusually large clitorises. In XX male syndrome (also called de la Chapelle syndrome) the resulting child is usually a phenotypically normal male, but without sperm production. This syndrome is sometimes the result of an abnormal There is a website that contains very easy to read information on this subject. http://www.isna.org/faq/what_is_intersex MstrssPassion
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