Alien DNA Found In A Two Year Old Boy

[Savwafair2012 Profile]

Two Year Old Child Becomes First Person in the world To Have Extra Strand Of DNA!!!



Is this the beginnings of Human NovaMan Mutations!?

"His parents Gemma and Richard Clamp only discovered something was wrong with their son after they first took him home.

Within days, he was rushed back to hospital after he stopped breathing and his lips turned blue.

Then when he was six weeks old, doctors discovered he had a rare abnormality in his DNA."

A two-year-old boy has become the only person in the world to be diagnosed with an extra strand in his DNA.
Brave Alfie Clamp was born blind and with severe disabilities, which led doctors to carry out various tests.

They revealed his seventh chromosome has an extra strand of material which has never been documented anywhere in the world before.
Doctors are baffled at his condition, which is so rare it does not have a name.
Baffling: Alfie Clamp, two, has an extra 'arm' on one of his chromosomes
Medics also have no idea whether his condition will improve or reduce his life expectancy.
Alfie, from Nuneaton, Warks., can now see and he will have an operation this month to fix an intestinal problem caused by his condition.
His parents Gemma and Richard Clamp only discovered something was wrong with their son after they first took him home.
Within days, he was rushed back to hospital after he stopped breathing and his lips turned blue.
Then when he was six weeks old, doctors discovered he had a rare abnormality in his DNA.
Mrs Clamp said: 'When the doctors told us I was absolutely devastated. As a pregnant mum you spend nine months thinking about what it will be like when your baby takes their first step or claps their hands.
'Having a boy like Alfie makes you appreciate the little things. He didn't roll over until he was 18 months old, but we were so excited when he did.'


A microscopic image of human chromosomes. Little Alfie Clamp has an 'extra arm' on one of his, in what is believed to be a world first.

His condition left Alfie unable to see until he was three months old and his muscles were so weak he could not roll over on his own.
He still suffers serious digestive problems and needs a cocktail of drugs every day to help his body absorb vital nutrients.

He also suffers fits which sparked by high temperatures and metabolic problems stop him from eating or drinking.

Since he was born, Alfie has been rushed to hospital six times - including twice just last month - when he stopped breathing.

His parents even believed he was dying twice and were stunned when Alfie made a full recovery after spending time in hospital.

Mr and Mrs Clamp, who also have 10-year-old daughter Georgia who is perfectly healthy, had their DNA tested but were not carriers of the faulty gene.
Mr Clamp said: 'The doctors told us there is nothing we could have done to prevent it. I don't think we'll ever know why it happened.

'I was holding him in my arms and I could see his eyes start to focus on me. It was a massive milestone for us because we didn't know if that would ever happen.
'We even took a photograph of the two of us sat there, looking at each other. Having Alfie has changed our lives - everything revolves around him. But he is such a happy boy and he has brought a lot of joy to our lives.

'Whenever we go to hospital, all the doctors and nurses say what a pleasure it is to see Alfie.'

http://www.dailymail.co.uk/health/artic ... d-DNA.html

[99socks Profile]

This isn't as weird as the article wants to make you think. Most people are not aware than it is quite possible to have two completely different sets of DNA, sitting in different parts of the body. It is more common than you think that some people's hair has DNA that is different from their kidneys. The fact that there is an "extra" strand isn't that weird either, considering that a duplicate copy of a chromosome is responsible for such disorders as Down's syndrome and more. The only thing that is unique is that in THIS situation, the child most likely has two sets of DNA, and that a cross-pollination of these has caused him to carry an extra piece in the set that was analyzed. Which of course, is a form of mutation.....

[Gunzenbomz Profile]

If you look deep enough you will find, humans on Earth have had Alien dna attached to the long arm dna for around 120-150 thousand years.

[Punjedi Profile Website]

I was about to start thinking, finally. Something that may lead to some real disclosure.


Wrong again. Once we do a little research into Chromosome 7, it starts to become
evident that this particular Chromosome has quite a long list of issues.

Almost all of them relating to developmental issues.


Firt off.

Chromosome 7 is one of the 23 pairs, it also happens to represent approx. 5.25 percent
of the total DNA in cells.

What is also interesting to note is that people normally have two copies of this Chromosome.


This leads one to wonder, did they test both pairs? Did both pairs exist? If so, did one pair reflect
the same anomoly as the other?

From Wiki -

The following diseases are some of those related to genes on chromosome 7:

argininosuccinic aciduria
cerebral cavernous malformation
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease, type 2
citrullinemia
congenital bilateral absence of vas deferens
cystic fibrosis
distal spinal muscular atrophy, type V
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome, arthrochalasia type
Ehlers-Danlos syndrome, classical type
hemochromatosis
hemochromatosis, type 3
hereditary nonpolyposis colorectal cancer
lissencephaly
maple syrup urine disease
maturity onset diabetes of the young type 2
mucopolysaccharidosis type VII or Sly syndrome
myelodysplastic syndrome
nonsyndromic deafness
nonsyndromic deafness, autosomal dominant
nonsyndromic deafness, autosomal recessive
osteogenesis imperfecta
osteogenesis imperfecta, type I
osteogenesis imperfecta, type II
osteogenesis imperfecta, type III
osteogenesis imperfecta, type IV
p47-phox-deficient chronic granulomatous disease
Pendred syndrome
Romano-Ward syndrome
Shwachman-Diamond syndrome
Schizophrenia
Tritanopia or tritanomaly color blindness
Williams syndrome


and these are some the Gene labels within Chromosome 7

ACHE acetylcholinesterase (Yt blood group) 7q22
1749 DLX5 distal-less homeobox 5 7q22
1750 DLX6 distal-less homeobox 6 7q22
2050 EPHB4 EPH receptor B4 7q22
3912 LAMB1 laminin, beta 1 7q22
4034 LRCH4 leucine-rich repeats and calponin homology (CH) domain containing 4 7q22
5649 RELN reelin 7q22
7205 TRIP6 thyroid hormone receptor interactor 6 7q22
10156 RASA4 RAS p21 protein activator 4 7q22
10603 SH2B2 SH2B adaptor protein 2 7q22
11062 DUS4L dihydrouridine synthase 4-like (S. cerevisiae) 7q22-q31

http://bioinfo.mc.vanderbilt.edu/SZGR/display/showGeneset.jsp?page=1


The point of all this is that within Chromosome 7 there are 189 Genes.

Each and every one of those Genes can create problems if it is either
missing/damaged/mutated.


For instance.

Gene Name: C7orf16 (Id) GSBS.

Long term depression.
http://www.genome.jp/dbget-bin/www_bget?hsa:10842


Gene Name: NDUFB2 (Id) 4708

KEGG Pathway info includes Alzheimer's and Parkinson's.
http://bioinfo.mc.vanderbilt.edu/SZGR/displayGenePage.do?geneid=4708



The overall point is that this is appears to be a problem within a Chromosome
that is already prone to mutations, genetic defects, and protein-protein interaction
problems.

Granted, they mentioned that this extra "arm" was not found in any of the parents/siblings
but had it been any other Chromosome I would think that there would be something of
extra-terrestrial value.

As it stands, I believe that once more is done to find out what caused this and what long-term
effects it will have, we will see it labeled as "Clamp's Disease".

Also, in case your wondering....

http://www.rsc.org/chemistryworld/Issues/2005/July/DNA.asp

"The DNA double helix can under certain conditions accommodate a third strand in its major groove. Researchers in the UK have now presented a complete set of four variant nucleotides that makes it possible to use this phenomenon in gene regulation and mutagenesis."


I think we will start to see more and more "mutations" of ourselves as we are constantly inundated
with chemicals, carcinogens, manufactured products and edibles, and the rise of high level science
that does admit to spraying, seeding, genetically altering our grains and crops.

Add that to the constant dizzying array of absolute junk that parents will feed their children or allow
them to consume and then wonder why they have developmental issues or problems with growth.

I am not saying that the Clamp's were in any way neglectful, but that it is possible through simple
"being unaware" of the contents and products that we give our children to eat, apply to their body/skin, or give them in some form of medication to fight whatever ails them, that the child
had to undergo a drastic genetic mutation to compensate or as a direct result of said product/produce.

The only thing alien about this story is that not one single doctor or DNA specialist has released
any periodical or study on this child, or at least one that can be found.

This is "world breaking news" but yet every single article I find is just either a re-hash or an exact
cut and copy of the same article, which naturally is found on everything from here to GLP, ATS, and many, many other "fringe" sites.

Yet again, another viral headline to overshadow the mundane and rather complex truth of the matter.

None of which, anyone really cares to find out.

It's so much COOLER to think of aliens and ufos right? Because, God forbid, anyone take an interest in real life and try and accomplish something worthwhile.

Like, learn how to truly map the Human Genome and find the benefits within.

Not posting headlines like "Alien in my DNA" or "Look who I just started having a crush on because FaceBook told me to"

-Peace-

[Ufologist Profile]

Not quite new...there are 2 other reports that I know of...one in Ohio, USA, and the other is in Puerto Rico. Both are female.

[Ademu Profile]

I was about to start thinking, finally. Something that may lead to some real disclosure.


Wrong again. Once we do a little research into Chromosome 7, it starts to become
evident that this particular Chromosome has quite a long list of issues.

Almost all of them relating to developmental issues.


Firt off.

Chromosome 7 is one of the 23 pairs, it also happens to represent approx. 5.25 percent
of the total DNA in cells.

What is also interesting to note is that people normally have two copies of this Chromosome.


This leads one to wonder, did they test both pairs? Did both pairs exist? If so, did one pair reflect
the same anomoly as the other?

From Wiki -

The following diseases are some of those related to genes on chromosome 7:

argininosuccinic aciduria
cerebral cavernous malformation
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease, type 2
citrullinemia
congenital bilateral absence of vas deferens
cystic fibrosis
distal spinal muscular atrophy, type V
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome, arthrochalasia type
Ehlers-Danlos syndrome, classical type
hemochromatosis
hemochromatosis, type 3
hereditary nonpolyposis colorectal cancer
lissencephaly
maple syrup urine disease
maturity onset diabetes of the young type 2
mucopolysaccharidosis type VII or Sly syndrome
myelodysplastic syndrome
nonsyndromic deafness
nonsyndromic deafness, autosomal dominant
nonsyndromic deafness, autosomal recessive
osteogenesis imperfecta
osteogenesis imperfecta, type I
osteogenesis imperfecta, type II
osteogenesis imperfecta, type III
osteogenesis imperfecta, type IV
p47-phox-deficient chronic granulomatous disease
Pendred syndrome
Romano-Ward syndrome
Shwachman-Diamond syndrome
Schizophrenia
Tritanopia or tritanomaly color blindness
Williams syndrome


and these are some the Gene labels within Chromosome 7

ACHE acetylcholinesterase (Yt blood group) 7q22
1749 DLX5 distal-less homeobox 5 7q22
1750 DLX6 distal-less homeobox 6 7q22
2050 EPHB4 EPH receptor B4 7q22
3912 LAMB1 laminin, beta 1 7q22
4034 LRCH4 leucine-rich repeats and calponin homology (CH) domain containing 4 7q22
5649 RELN reelin 7q22
7205 TRIP6 thyroid hormone receptor interactor 6 7q22
10156 RASA4 RAS p21 protein activator 4 7q22
10603 SH2B2 SH2B adaptor protein 2 7q22
11062 DUS4L dihydrouridine synthase 4-like (S. cerevisiae) 7q22-q31

http://bioinfo.mc.vanderbilt.edu/SZGR/display/showGeneset.jsp?page=1


The point of all this is that within Chromosome 7 there are 189 Genes.

Each and every one of those Genes can create problems if it is either
missing/damaged/mutated.


For instance.

Gene Name: C7orf16 (Id) GSBS.

Long term depression.
http://www.genome.jp/dbget-bin/www_bget?hsa:10842


Gene Name: NDUFB2 (Id) 4708

KEGG Pathway info includes Alzheimer's and Parkinson's.
http://bioinfo.mc.vanderbilt.edu/SZGR/displayGenePage.do?geneid=4708



The overall point is that this is appears to be a problem within a Chromosome
that is already prone to mutations, genetic defects, and protein-protein interaction
problems.

Granted, they mentioned that this extra "arm" was not found in any of the parents/siblings
but had it been any other Chromosome I would think that there would be something of
extra-terrestrial value.

As it stands, I believe that once more is done to find out what caused this and what long-term
effects it will have, we will see it labeled as "Clamp's Disease".

Also, in case your wondering....

http://www.rsc.org/chemistryworld/Issues/2005/July/DNA.asp

"The DNA double helix can under certain conditions accommodate a third strand in its major groove. Researchers in the UK have now presented a complete set of four variant nucleotides that makes it possible to use this phenomenon in gene regulation and mutagenesis."


I think we will start to see more and more "mutations" of ourselves as we are constantly inundated
with chemicals, carcinogens, manufactured products and edibles, and the rise of high level science
that does admit to spraying, seeding, genetically altering our grains and crops.

Add that to the constant dizzying array of absolute junk that parents will feed their children or allow
them to consume and then wonder why they have developmental issues or problems with growth.

I am not saying that the Clamp's were in any way neglectful, but that it is possible through simple
"being unaware" of the contents and products that we give our children to eat, apply to their body/skin, or give them in some form of medication to fight whatever ails them, that the child
had to undergo a drastic genetic mutation to compensate or as a direct result of said product/produce.

The only thing alien about this story is that not one single doctor or DNA specialist has released
any periodical or study on this child, or at least one that can be found.

This is "world breaking news" but yet every single article I find is just either a re-hash or an exact
cut and copy of the same article, which naturally is found on everything from here to GLP, ATS, and many, many other "fringe" sites.

Yet again, another viral headline to overshadow the mundane and rather complex truth of the matter.

None of which, anyone really cares to find out.

It's so much COOLER to think of aliens and ufos right? Because, God forbid, anyone take an interest in real life and try and accomplish something worthwhile.

Like, learn how to truly map the Human Genome and find the benefits within.

Not posting headlines like "Alien in my DNA" or "Look who I just started having a crush on because FaceBook told me to"

-Peace-

Damn Pun you had to ruin this thread by using your brain and a little science. Shame on you sir