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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 question “are men xx?” challenges this basic understanding by raising curiosity about exceptions or anomalies in chromosomal patterns [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.
Sex chromosomes are the genetic elements that define a person's biological sex Without this gene, the embryo usually develops female characteristics Learn about the xx and xy chromosomes, the sex determination system, and other chromosome combinations.
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.
A rare disorder where individuals with two x chromosomes develop male characteristics due to sry gene translocation. Xx male syndrome is defined as a disorder of sex development in which individuals have a 46,xx chromosomal pattern but present with male external genitalia and often experience conditions such as delayed puberty, infertility, or gynecomastia Ai generated definition based on What is xx male syndrome
Xx male syndrome is a rare intersex condition in which an individual with a 46,xx karyotype develops a male phenotype.
The presence of a y chromosome generally leads to male development because it carries the sry gene, a key factor in initiating testes formation
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