×
Create a new article
Write your page title here:
We currently have 7,685 articles on LGBTQIA+ Wiki. Type your article name above or create one of the articles listed here!



    LGBTQIA+ Wiki
    7,685Articles

    Tetrasomy X: Difference between revisions

    Content added Content deleted
    No edit summary
    No edit summary
    Line 2: Line 2:
    '''Tetrasomy X''', '''XXXX syndrome''', '''quadruple X''', or '''48,XXXX''' is an [[intersex]] trait that occurs in [[AFAB]]/[[CTF]] individuals, in which they are born with four X chromosomes rather than only the expected two. It appears to be rare, as approximately 100 cases have been reported worldwide, however there may be unspoken cases of the past, as people with this condition can usually function decently well, despite the physical abnormalities that co-side this condition.<ref>https://en.wikipedia.org/wiki/Tetrasomy_X</ref>
    '''Tetrasomy X''', '''XXXX syndrome''', '''quadruple X''', or '''48,XXXX''' is an [[intersex]] trait that occurs in [[AFAB]]/[[CTF]] individuals, in which they are born with four X chromosomes rather than only the expected two. It appears to be rare, as approximately 100 cases have been reported worldwide, however there may be unspoken cases of the past, as people with this condition can usually function decently well, despite the physical abnormalities that co-side this condition.<ref>https://en.wikipedia.org/wiki/Tetrasomy_X</ref>


    The traits that usually come along with this condition is often very similar to traits within the [[Triple X Syndrome|triple X syndrome.]] They often are born with epicanthal folds, flat nasal bridges, a small mouth or underdeveloped face, delayed or absent teeth, enamel defects, joint and muscle tone abnormalities, spine and hip abnormalities, and are often taller than average. They may also have an abnormal nervous system, abnormal hearing/vision, abnormal circulatory systems, and abnormal kidneys.
    The traits that usually come along with this condition is often very similar to traits within the [[Triple X Syndrome|triple X syndrome.]] They often are born with epicanthal folds, flat nasal bridges, a small mouth or underdeveloped face, delayed or absent teeth, enamel defects, joint and [[Secondary Sex Agenesis|muscle tone abnormalities]], spine and hip abnormalities, and are often taller than average. They may also have an abnormal nervous system, abnormal hearing/vision, abnormal circulatory systems, and abnormal kidneys.


    Ones with this condition often experience mild delays in the areas of speech development and articulation, language expression and understanding, and reading skills. Delays in motor development are also present, with walking ages ranging from 16 months to 4.5 years. Despite this fact, brain scans haven't shown any abnormalities within the brain of these individuals.
    Ones with this condition often experience mild delays in the areas of speech development and articulation, language expression and understanding, and reading skills. Delays in motor development are also present, with walking ages ranging from 16 months to 4.5 years. Despite this fact, brain scans haven't shown any abnormalities within the brain of these individuals.
    Cookies help us deliver our services. By using our services, you agree to our use of cookies.
    Cookies help us deliver our services. By using our services, you agree to our use of cookies.