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    Campomelic Dysplasia or Campomelic Syndrome is an intersex variation that effects 1 in 40,000 to 200,000 individuals in which ones reproductive system, bone structure, and genitals are developed oddly, underdeveloped, or extremely misplaced. This variation is known as the most dangerous intersex variations, as 95% of cases end in death during infancy. This variation can effect both AMAB/CTM and AFAB/CTF individuals.[1]

    Those with this variation usually have short legs, dislocated hips, underdeveloped shoulder blades, eleven ribs instead of the usual twelve, neck abnormalities, upward-turning feet, a small chin, prominent eyes, a flat face, and a larger head than usual. They may also have laryngotracheomalacia, which causes issues with breathing, and is the main cause of death within those with this variation. They may or may not be born with bent or bowed limbs, however the rest of the symptoms usually still apply regardless.[2]

    Among CTM individuals, 75% of individuals with this variation are born with ambiguous genitals or a vagina, despite their XY chromosomes. Among both CTM and CTF individuals, they can have either a wolffian reproductive system, a müllerian reproductive system, or a combination (ovotesticular.)

    Those who survive with this variation often grow up to have scoliosis, hearing issues, and mental disabilities. Some of the symptoms may classify one with this variation as physically disabled.

    Causes

    This variation is most often caused when ones SOX9 gene is mutated. This gene usually regulates protein production, and if it does not work properly, the protein may be overproduced or underproduced, causing physical abnormalities when one is still in the fetus stage.

    Etymology

    The term campomelic comes from the Greek words for "bent limb."

    References

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