Human genome 6
postmaster at 127.0.0.1
Tue Jul 10 11:14:13 EST 2001
Anders Gorm Pedersen wrote:
> Gandalf Parker wrote:
> > I have a son who was diagnosed C6p+ 20 years ago by military doctors.
> > They did a few papers on him and had us prepare for an early death. They
> > did some searchs of world medical librarys and found no matchs (none
> > that werent ummmm trans-locates? something like that)
> - Gandalf (very nice name by the way!)
Well it used to be unique until I got on the internet. Now I cant use it
anywhere because some kid has snagged it as a handle. But as far as I know Im
oneof the few people who really have it as a name. Love the looks when they say
"is that german?" and I reply "no, its elvan".
> genetic material, compared to a normal chromosome 6. In some cases this can
> be caused by a so-called translocation. Put simply, that's when a piece of
> one chromosome has "broken off" and gotten attached to another chromosome.
> (But apparently that was not the case for your son.)
Good read. Yes its extra protein with no trans-locate. We dont really consider
it a disorder. It has its Pros and Cons. Dont want to set anyone off here since
this isnt my group but they referred to it as "spontaneus natural mutation"
which I was actualy able to accept easier than disorder.
> There has been tremendous progress in the ability of doctors to analyze
> chromosomes over the past 20 years, and chances are that a lot more
> information is available now. However, there are two caveats: (1) there are
> so many possible chromosomal disorders that any particular one may be
> unique, having no exact matches in any other person. (2) The ability
> to characterize chromosome aberrations does far from always translate into
> knowledge about how to best help a person with that particular disorder.
He is 22 years old now. Wasnt supposed to live past 6 based on the only info
availalble at the time but all of those were trans-locates. Its just that since
I retired from the military there isnt really any doctors forwarding info or
watching for any. Im wondering if I should get in contact with anyone to insure
that info he can provide the databases is being included. Is there a central
clearing house in the USA for the human phenome project?
Oh, thank you for the RareChromo.org link. That looks quite interesting.
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