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Xx male syndrome, also known as de la chapelle syndrome or 46,xx testicular disorder of sex development (or 46,xx dsd) is a rare intersex condition in which an individual with a 46,xx karyotype develops a male phenotype The patients can live a fairly normal life but like all disorders, they require a strong social support system, in the presence of which the quality of life is greatly improved. [2][3][4][5][6] in 90 percent of these individuals, the syndrome is caused by the father's y chromosome 's sry gene being atypically included in the crossing over of genetic.
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In human biology, the typical understanding of sex determination is that biological men have xy chromosomes, while biological women have xx chromosomes. With hormonal replacement, therapy, surgery and multidisciplinary follow up the prognosis of xx male syndrome is good Sex chromosomes are the genetic elements that define a person's biological sex
Learn about the xx and xy chromosomes, the sex determination system, and other chromosome combinations.
Understanding xx male syndrome xx male syndrome, also known as de la chapelle syndrome, is a condition where an individual has two x chromosomes, which are typically associated with female genetic sex, but exhibits male external genitalia and internal reproductive structures. A rare disorder where individuals with two x chromosomes develop male characteristics due to sry gene translocation. Xx male syndromedefinitionxx male syndrome occurs when the affected individual appears as a normal male, but has female chromosomes Two types of xx male syndrome can occur
Those with detectable sry gene and those without detectable sry (sex determining region y) Sry is the main genetic switch for determining that a developing embryo will become male Source for information on xx male. What is the prognosis of xx male syndrome
