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    WNT4 Deficiency: Difference between revisions

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    [[File:Wnt4.jpg|thumb|200x200px|The WNT4 Deficency flag.]]
    [[File:Wnt4.jpg|thumb|200x200px|The WNT4 Deficency flag.]]
    '''WNT4 Deficiency''' is an [[intersex]] condition that effects [[CTF]] individuals. Those with this condition usually also have [[Müllerian Agenesis]], however this condition is rarer than Müllerian Agenesis, meaning those with Müllerian Agenesis usually do not have this condition.
    '''WNT4 Deficiency''' is an [[intersex]] variation that effects [[CTF]] individuals. Those with this variation usually also have [[Müllerian Agenesis]], however this variation is rarer than Müllerian Agenesis, meaning those with Müllerian Agenesis usually do not have this variation.


    Those with this condition have an [[Agenital|underdeveloped or absent vagina]], [[Ambiguous Genitalia|ambiguous genitals]], an underdeveloped or absent uterus, and [[hyperandrogenism]]. Because of this, they develop acne, amenorrhea, and extra body hair.
    Those with this variation have an [[Agenital|underdeveloped or absent vagina]], [[Ambiguous Genitalia|ambiguous genitals]], an underdeveloped or absent uterus, and [[hyperandrogenism]]. Because of this, they develop acne, amenorrhea, and extra body hair.


    They may experience pain during sexual intercourse, urinary tract infections, and/or kidney stones however this is not always the case.
    They may experience pain during sexual intercourse, urinary tract infections, and/or kidney stones however this is not always the case.


    == Causes ==
    == Causes ==
    WNT4 Deficiency is caused by mutations in the ''WNT4'' gene. This genetic mutation can occur randomly as a spontaneous event (i.e., new mutation) or it can be inherited from parents. This is due to an abnormal gene that one or both parents could have within their system. If both parents have it, the condition will be more severe when passed down to the child.
    WNT4 Deficiency is caused by mutations in the ''WNT4'' gene. This genetic mutation can occur randomly as a spontaneous event (i.e., new mutation) or it can be inherited from parents. This is due to an abnormal gene that one or both parents could have within their system. If both parents have it, the variation will be more severe when passed down to the child.


    == Flag ==
    == Flag ==
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