Please Identify

>what the FUCK is wrong with this girl

She's from Georgia. Next question.

File: autismspeaks.gif (2MB, 480x270px)

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>igor has a job and you don't

>Loves: God
he doesn't love you back sweetheart

Featle Alchohol Syndndrome or Fraigile X. Why? Are you thinking of fucking her? Don't worry she wont remember,

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>tinder account
>"hurr fuck me, chad! fuck me, chad!"

It's absolutely disgusting to see how entitled she is. Is she cognizant of how off-puting her face is?
Atleast we robots have enough decency to hole ourselves off from the normie-world instead of subjecting others to eye torture.

>>34374921

>her inbox is full anyway
>she won't settle for less than a 8/10

>>34375049
>Featle Alchohol Syndndrome or Fraigile X
There is so much wrong with this post

>>34374921
URUK!!!

>>34375567
GRAVEWALKER

>>34374921
please swipe right anon
or superlike
I really want to see this

>>34374921
>Gordon State College
>Barnesville, Georgia
>the south
mystery solved

Somebody call that girl who fucked the downy kid in that other thread, I think I found a girl she can experiment with.

>>34375547
There is nothing wrong with this post m8 unless you're talking up the ass or down the cunt. As far as I'm concerned you're a great fucking bunch of pissfaps conectected like a sprinkler.

>>34376339
it was the spelling of the disorders, dumbass, not that anon was pointing out the likelihoods of her having them

>>34374921

Crouzon Syndrome

It is an autosomal dominant genetic disorder also known as branchial arch syndrome.

This syndrome is caused by a mutation in the fibroblast growth factor receptor II, located on chromosome 10.

Incidence of Crouzon syndrome is currently estimated to occur in 1.6 out of every 100,000 people. It tends to run in families, specifically those practicing consanguinity.

For reasons that are not entirely clear, most Crouzon patients also have noticeably shorter humerus and femur bones relative to the rest of their bodies than members of the general population. A small percentage of Crouzon patients also have what is called "Type II" Crouzon syndrome, distinguished by partial syndactyly.

If treated with surgery while still very young, a person with Crouzon Syndrome, can be expected to live a normal lifespan, depending upon the severity of any neruological impairment most Crouzon Syndrome patients may need only minor assistance to function independently as adults.