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'''17-AH Deficiency''' or '''17-alpha-hydroxylase deficiency''' is an [[intersex]] variation in which the adrenal glands- the glands that regulate the production of certain horomones- do not properly function. Because of this, the reproductive system does not grow very strongly. This condition is estimates to effect 1 in a million individuals at birth.
Those with XX chromosomes ([[CTF]]) have abnormally small ovaries and an abnormally small uterus. Because of this, they [[Secondary Sex Agenesis|do not develop many secondary sex traits]], such as breasts, pubic hair, or menstruation cycles. From this, they are unable to
Those with XY chromosomes ([[CTM]]) usually have [[Ambiguous Genitalia|ambiguous genitals]] or a vagina, and because of this, they are often mistaken as female. Those that do have a penis often have a [[Agenital|micropenis, cryptorchidism,]] and/or [[hypospadias]]. They are also infertile, and often fall under [[AMAB Hypogonadism]].
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== Genetics ==
This variation is inherited in an ''autosomal recessive pattern,'' which means both parents have a copy of the gene mutation that causes this, and both of their genes combined is what effected the child when being
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