A little hope

B

BaylorCrew07

New member
ADawn00 - I'm sorry for the limbo you guys have been in and everything you are going through. Congrats on the good news. <img src="i/expressions/face-icon-small-smile.gif" border="0">

I have NEVER heard anything like this; I always though 2 mutations = CF regardless.

This <a target=_blank class=ftalternatingbarlinklarge href="http://www.rmlonline.com/patientCen.asp?id=ss161">info</a> seems to imply that that is not always the case.

"This [genetic] test will detect the <b>F508C MUTATION, a non-cystic fibrosis (CF)-causing variant</b>. When the F508C mutation is paired with a CF-causing mutation, it has been associated with congenital bilateral absence or atresia of the vas deferens (CBAVD). "
 
B

BaylorCrew07

New member
ADawn00 - I'm sorry for the limbo you guys have been in and everything you are going through. Congrats on the good news. <img src="i/expressions/face-icon-small-smile.gif" border="0">

I have NEVER heard anything like this; I always though 2 mutations = CF regardless.

This <a target=_blank class=ftalternatingbarlinklarge href="http://www.rmlonline.com/patientCen.asp?id=ss161">info</a> seems to imply that that is not always the case.

"This [genetic] test will detect the <b>F508C MUTATION, a non-cystic fibrosis (CF)-causing variant</b>. When the F508C mutation is paired with a CF-causing mutation, it has been associated with congenital bilateral absence or atresia of the vas deferens (CBAVD). "
 
B

BaylorCrew07

New member
ADawn00 - I'm sorry for the limbo you guys have been in and everything you are going through. Congrats on the good news. <img src="i/expressions/face-icon-small-smile.gif" border="0">

I have NEVER heard anything like this; I always though 2 mutations = CF regardless.

This <a target=_blank class=ftalternatingbarlinklarge href="http://www.rmlonline.com/patientCen.asp?id=ss161">info</a> seems to imply that that is not always the case.

"This [genetic] test will detect the <b>F508C MUTATION, a non-cystic fibrosis (CF)-causing variant</b>. When the F508C mutation is paired with a CF-causing mutation, it has been associated with congenital bilateral absence or atresia of the vas deferens (CBAVD). "
 
B

BaylorCrew07

New member
ADawn00 - I'm sorry for the limbo you guys have been in and everything you are going through. Congrats on the good news. <img src="i/expressions/face-icon-small-smile.gif" border="0">

I have NEVER heard anything like this; I always though 2 mutations = CF regardless.

This <a target=_blank class=ftalternatingbarlinklarge href="http://www.rmlonline.com/patientCen.asp?id=ss161">info</a> seems to imply that that is not always the case.

"This [genetic] test will detect the <b>F508C MUTATION, a non-cystic fibrosis (CF)-causing variant</b>. When the F508C mutation is paired with a CF-causing mutation, it has been associated with congenital bilateral absence or atresia of the vas deferens (CBAVD). "
 
B

BaylorCrew07

New member
ADawn00 - I'm sorry for the limbo you guys have been in and everything you are going through. Congrats on the good news. <img src="i/expressions/face-icon-small-smile.gif" border="0">
<br />
<br />I have NEVER heard anything like this; I always though 2 mutations = CF regardless.
<br />
<br />This <a target=_blank class=ftalternatingbarlinklarge href="http://www.rmlonline.com/patientCen.asp?id=ss161">info</a> seems to imply that that is not always the case.
<br />
<br />"This [genetic] test will detect the <b>F508C MUTATION, a non-cystic fibrosis (CF)-causing variant</b>. When the F508C mutation is paired with a CF-causing mutation, it has been associated with congenital bilateral absence or atresia of the vas deferens (CBAVD). "
 
You must log in or register to reply here.
Top