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my little ones mutations the docs say it is a rare one?????
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A
age
Guest
my little ones mutations the docs say it is a rare one?????
A
age
Guest
my little ones mutations the docs say it is a rare one?????
A
age
Guest
my little ones mutations the docs say it is a rare one?????
A
age
Guest
my little ones mutations the docs say it is a rare one?????
Hi,
I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
Good luck!
Sarah
(G551/R75Q, 32 years old, still awaiting official diagnosis)
I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
Good luck!
Sarah
(G551/R75Q, 32 years old, still awaiting official diagnosis)
Hi,
I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
Good luck!
Sarah
(G551/R75Q, 32 years old, still awaiting official diagnosis)
I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
Good luck!
Sarah
(G551/R75Q, 32 years old, still awaiting official diagnosis)
Hi,
I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
Good luck!
Sarah
(G551/R75Q, 32 years old, still awaiting official diagnosis)
I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
Good luck!
Sarah
(G551/R75Q, 32 years old, still awaiting official diagnosis)
Hi,
I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
Good luck!
Sarah
(G551/R75Q, 32 years old, still awaiting official diagnosis)
I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
Good luck!
Sarah
(G551/R75Q, 32 years old, still awaiting official diagnosis)
Hi,
<br />
<br />I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
<br />
<br />I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
<br />
<br />Good luck!
<br />Sarah
<br />(G551/R75Q, 32 years old, still awaiting official diagnosis)
<br />
<br />I don't have these mutations, but I wasn't able to find anyone with mine either. There are so many, you may not run across someone with the same combination as you, especially if one is really rare.
<br />
<br />I'm very new to this board, but from what I've learned so far, you really can't predict anything based on the mutations you have. So if you do find someone else with the same genotype, your little ones could still have an easier or a harder time of things.
<br />
<br />Good luck!
<br />Sarah
<br />(G551/R75Q, 32 years old, still awaiting official diagnosis)
Hi! my friend's baby has been diagnosed as genotype DF508/E831X, he is only 10 months old, but is in very good health, without any lung or pancreatic symptoms at present.
Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
Let's hope in a favourable prognosis!
ale
Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
Let's hope in a favourable prognosis!
ale
Hi! my friend's baby has been diagnosed as genotype DF508/E831X, he is only 10 months old, but is in very good health, without any lung or pancreatic symptoms at present.
Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
Let's hope in a favourable prognosis!
ale
Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
Let's hope in a favourable prognosis!
ale
Hi! my friend's baby has been diagnosed as genotype DF508/E831X, he is only 10 months old, but is in very good health, without any lung or pancreatic symptoms at present.
Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
Let's hope in a favourable prognosis!
ale
Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
Let's hope in a favourable prognosis!
ale
Hi! my friend's baby has been diagnosed as genotype DF508/E831X, he is only 10 months old, but is in very good health, without any lung or pancreatic symptoms at present.
Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
Let's hope in a favourable prognosis!
ale
Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
Let's hope in a favourable prognosis!
ale
Hi! my friend's baby has been diagnosed as genotype DF508/E831X, he is only 10 months old, but is in very good health, without any lung or pancreatic symptoms at present.
<br />Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
<br />Let's hope in a favourable prognosis!
<br />
<br />ale
<br />Doctors still wait for diagnosis, because few cases with such genotype have been detected until now and no one among these with classical CF symptoms..
<br />Let's hope in a favourable prognosis!
<br />
<br />ale
Sickkids database has the E831X mutation listed with G551D, but not paired with DF508.
<a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
Sickkids database has the E831X mutation listed with G551D, but not paired with DF508.
<a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
Sickkids database has the E831X mutation listed with G551D, but not paired with DF508.
<a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
Sickkids database has the E831X mutation listed with G551D, but not paired with DF508.
<a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
Sickkids database has the E831X mutation listed with G551D, but not paired with DF508.
<br />
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>
<br />
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://cvs.genet.sickkids.on.ca:8080/penguin/MutationDetailPage.external?sp=370">http://cvs.genet.sickkids.on.c...ilPage.external?sp=370</a>