×
Create a new article
Write your page title here:
We currently have 7,591 articles on LGBTQIA+ Wiki. Type your article name above or create one of the articles listed here!



    LGBTQIA+ Wiki
    7,591Articles

    H Syndrome: Difference between revisions

    Content added Content deleted
    (Created page with "'''H Syndrome''', '''Histiocytosis-lymphadenopathy plus syndrome''', or '''PHID''' that may or may not be considered an intersex condition, or it may be considered a condi...")
     
    m (added category)
     
    (13 intermediate revisions by 4 users not shown)
    Line 1: Line 1:
    [[File:H syndrome.jpg|thumb|The H syndrome flag.]]
    '''H Syndrome''', '''Histiocytosis-lymphadenopathy plus syndrome''', or '''PHID''' that may or may not be considered an [[intersex]] condition, or it may be considered a condition that comes with intersex traits, depending on who you ask.
    '''H Syndrome''', '''Histiocytosis-Lymphadenopathy Plus Syndrome''', or '''PHID''', is a syndrome that may or may not be considered an [[intersex]] variation, or it may be considered a syndrome that comes with intersex traits, depending on who you ask.<ref>https://en.wikipedia.org/wiki/H_syndrome</ref>


    Those with this condition tend to have [[hypogonadism]], darker than usual skin (hyperpigmentation,) more hair growth than usual (hypertrichosis,) hearing loss, heart anomalies, low height, hyperglycemia, hallux valgus, and hepatosplenomegaly (enlarged spleen and liver.)
    Those with this syndrome tend to have [[hypogonadism]], darker skin than usual for their race (hyperpigmentation), more hair growth than usual (hypertrichosis), hearing loss, heart anomalies, low height, hyperglycemia, hallux valgus, and hepatosplenomegaly (enlarged spleen and liver).

    It is important to note that not all the symptoms listed in this page are guaranteed to occur in someone with this syndrome, as someone may only experience one or several of these symptoms, yet still hold the syndrome.


    == Causes ==
    == Causes ==
    This condition is caused by a mutation within the SLC29A3 gene, which is a gene that helps encode important proteins within the human body.
    This syndrome is caused by a mutation within the ''SLC29A3'' gene, which is a gene that helps encode important proteins within the biological human body.


    == History ==
    == History ==
    This condition was first described in 1998.
    This syndrome was first described in 1998.<ref>https://en.wikipedia.org/wiki/H_syndrome#History</ref>

    == Flag ==
    The H Syndrome flag was coined by [[User:Reign of the breadsticcs|Reign of the breadsticcs]] on May 7th of 2021. It has no confirmed meaning.<ref>https://lgbta.wikia.org/f/p/4400000000000137332/r/4400000000000449105</ref>


    == Etymology ==
    == Etymology ==
    This condition was named "H Syndrome" due to most of the symptoms starting with the letter H.
    This syndrome was named "H Syndrome" due to most of the symptoms starting with the letter H.


    == Resources ==
    == Resources ==
    <references />

    [[Category:Intersex Traits]]
    * https://en.wikipedia.org/wiki/H_syndrome
    [[Category:Verified Resources]]
    * https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838761/#:~:text=H%20syndrome%20is%20a%20rare,low%20height%2C%20and%20hallux%20valgus.
    [[Category:Sex Category]]
    * https://ped-rheum.biomedcentral.com/articles/10.1186/s12969-017-0204-y
    [[Category:Identities With unarchived resources]]

    Latest revision as of 22:16, 7 February 2022

    The H syndrome flag.

    H Syndrome, Histiocytosis-Lymphadenopathy Plus Syndrome, or PHID, is a syndrome that may or may not be considered an intersex variation, or it may be considered a syndrome that comes with intersex traits, depending on who you ask.[1]

    Those with this syndrome tend to have hypogonadism, darker skin than usual for their race (hyperpigmentation), more hair growth than usual (hypertrichosis), hearing loss, heart anomalies, low height, hyperglycemia, hallux valgus, and hepatosplenomegaly (enlarged spleen and liver).

    It is important to note that not all the symptoms listed in this page are guaranteed to occur in someone with this syndrome, as someone may only experience one or several of these symptoms, yet still hold the syndrome.

    Causes

    This syndrome is caused by a mutation within the SLC29A3 gene, which is a gene that helps encode important proteins within the biological human body.

    History

    This syndrome was first described in 1998.[2]

    Flag

    The H Syndrome flag was coined by Reign of the breadsticcs on May 7th of 2021. It has no confirmed meaning.[3]

    Etymology

    This syndrome was named "H Syndrome" due to most of the symptoms starting with the letter H.

    Resources

    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.