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Blackpill 22q gene deletion - you probably have it! (very popular gene defect)

AsiaCel

AsiaCel

Genocide all non-Mongoloid (and mutts) out of Asia
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My youngest brother has almost all symptoms of 22q. Mentally retarded, autistic, ADHD and associated facial traits. His face is gracile, with the tradesmark hooded eyes associated with the disorder.

Since 30% of the forum is autistic....

That has led me to do a little bit of research on 22q deletion syndrome....

1748017992317


It varies from person to person, but can have mild symptoms.
The phenotype of 22q11DS varies widely and across the age spectrum but usually includes hypocalcaemia with hypoparathyroidism, congenital heart defects (CHDs), typically conotruncal anomalies, palatal abnormalities, intellectual disability, variable facial dysmorphism and developmental delay, as well as thymic

People diagnosed are commonly associated with autism spectrum disorders
22q11.2 deletion syndrome (22q11.2DS) is a genomic disorder reported to associate with autism spectrum disorders (ASDs) in 15–50% of cases; however, others suggest that individuals with 22q11.2DS present psychiatric or behavioral features associated with ASDs, but do not meet full criteria for ASD diagnoses. Such wide variability in findings may arise in part due to methodological differences across studies. Our study sought to determine whether individuals with 22q11.2DS meet strict ASD diagnostic criteria using research-based guidelines from the Collaborative Programs of Excellence in Autism (CPEA), which required a gathering of information from three sources: the Autism Diagnostic Interview-Revised (ADI-R), the Autism Diagnostic Observational Schedule (ADOS), and a clinician’s best-estimate diagnosis. Our study examined a cohort of children, adolescents, and young adults (n = 56) with 22q11.2DS, who were ascertained irrespective of parents’ behavioral or developmental concerns, and found that 17.9% (n = 10) of the participants met CPEA criteria for an ASD diagnosis, and that a majority showed some level of social-communication impairment or the presence of repetitive behaviors. We conclude that strictly defined ASDs occur in a substantial proportion of individuals with 22q11.2DS, and recommend that all individuals with 22q11.2DS be screened for ASDs during early childhood.

This gene defect is very popular population speaking, because most indivdiuals live normal lives with minor defects and never got diagnosed. However, it has 50% of passing down to a child, and how the child gets affected is a guessing game.

Something to comfort you about: 90% is a new mutant of the new birth itself. Only 10% are inherited.

We can only pray for genetic engineering to advance...
 
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I hope CRISPR will save us from this nightmare! :feelsautistic::feelsautistic::feelsautistic:
Yeah, it's a very cruel disorder. I hope my youngest brother dies peacefully in a sleep (since heart disorders are common) He's clearly suffering a lot, and is a burden to the rest of us. When a case of severe disorder happens, it wrecks havoc on everyone around them.
 
I hope CRISPR will save us from this nightmare! :feelsautistic::feelsautistic::feelsautistic:
Furthermore, I'm convinced that most people carry some form of genetic defect, with minor phenotypical expression. Ready to strike at any moment (newbirths)
 
i probably have this . sterilise everyone who possesses this defect
 
and euthanise them too
 

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