It is named after two twins, Usually known as just Progeria, this condition is one that only affects one in about 8 million children born. on the other hand why are people not asking themselves , why are at least 2000/3000 people a day regeristing themselves and their fams’ with this disease. SETBP1 disorder is an extremely rare genetic neurodevelopmental disorder in which there is a variation (mutation) in the SETBP1 gene. Babies today are being born with this pathetic, horrid, disturbing disease which are causing all kinds of health problems to the child/ren ie severe headaches or burning pins nd needles to top/bk of head, nausia/stomach pains evry single day, numbness in joints, constant dental pain even after a visit to the dentist ( thnk they get fed up of seeing the same kids wk after wk/ or couple times a month because the dentist cant see anything wrong with the teeth and dont see anything wrong in painting there little teeth with ‘FLUORIDE’). there is a large amount of proof all over the internet, so if you cant be bothered to search and learn more about it or about the sane people who have it, well thats your lookout just plz leave the insults out, because youll be begging these sites for a cure for you soon enough.
Because of this, the disease is said to be extremely rare. I experience biting, crawling AND itching sensations and minor lesions resulting from scratching but not fatigue,memory loss i experience seems normal. In most cases, polio causes paralysis and muscle weakness. But then they didn’t recognize Lyme disease either for a long time.Alex my comment stands.
And since this list included congenital abnormalities, how about fetus in fetu and parasitic twins–both have only had 50-100 known in modern medicine.And one of the rarest of all–craniopagus parasiticus. Progeria is a genetic condition that occurs due to a new mutation characterized by the dramatic, rapid appearance of aging beginning in childhood. !ALEX, Have you met karma?
Sadly, the disease is usually disfiguring as well as disabling. :'( I researching for my project on gentic diseases. Those with Morgellons claim to find fibers in sores and whatnot and there is no medical truth to any of those claims.you are a typical stereotyped brainwashed good little American as I once was, I like you once believed what the major medical establishments claimed to be fact. This is the part that the extract for the pesticide. You are doing that to yourself just fine. I live in AZ and this summer i suffered when it was humid. Aboulomania; If you find it hard to make decisions, spare a thought for people with aboulomania. Keratinocytes, which are what make up the epidemus, separate from each other, leaving gaps. ?Field’s disease sure sounds like Lou Gerhig’s disease (ALS) to me.I thought this is an article on the rarest…..how did the last 3 count? The condition affects one in eight million live births and those born with progeria typically live to their mid-teens to early twenties.The condition occurs as a new mutation and is rarely inherited as carriers usually do not live to reproduce. This was all extremely helpful yet traumatizing to my emotions Morgellons is poorly known to most doctors because it doesn’t exist. The support groups for Morgellons are the same people who believe that the contrails from airplanes are really secret government chemicals that are dropped on the people, in fact they’re starting to say that that’s where Morgellons comes from.Alex go get yourself a life and if thats a wee bit hard for you why not try taking a parachute jump into the jungle, worst is that can happen is being caugt by cannibals or a lion, maybe a croc! How dare you insult the those suffering from morgs’ it is 100% real and you are arrogant. Take a second to support Toptenz.net on Patreon! I used to work with a guy who I think had Morgellons. There are still 30,000 to 50,000 cases of viral or aseptic meningitis every year. Many believe that smallpox was one of the deadliest diseases, killing around 300-500 million in the 20th century, in 400,000 each year throughout the 18th century. On the other hand there is a lot of proof that it is. Somewhat uncommon yet not as rare as Liam Hoekstra’s super strength, doctors know a great deal about this syndrome and how to treat those who have it.
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