Does ANYONE know about these.....

steffer73

New member
Hey there,
I have a 14 yr old son w/ CF and he has had a pretty hard time the past 3 yrs. We have been sent to get the double lung evaluation. We have started the prelim. tests to find out where he stands, but I was just told his genotypes (R560T/621+1G).....AND I can't find any info!!! I just want to know some stuff about them and all I can find is info on delta F508.
If you know where I can get some info I would greatly appreciate it<img src="i/expressions/face-icon-small-smile.gif" border="0">

Thanks
Stephanie
Mom of 14 yr old son w/ CF
 

steffer73

New member
Hey there,
I have a 14 yr old son w/ CF and he has had a pretty hard time the past 3 yrs. We have been sent to get the double lung evaluation. We have started the prelim. tests to find out where he stands, but I was just told his genotypes (R560T/621+1G).....AND I can't find any info!!! I just want to know some stuff about them and all I can find is info on delta F508.
If you know where I can get some info I would greatly appreciate it<img src="i/expressions/face-icon-small-smile.gif" border="0">

Thanks
Stephanie
Mom of 14 yr old son w/ CF
 

steffer73

New member
Hey there,
I have a 14 yr old son w/ CF and he has had a pretty hard time the past 3 yrs. We have been sent to get the double lung evaluation. We have started the prelim. tests to find out where he stands, but I was just told his genotypes (R560T/621+1G).....AND I can't find any info!!! I just want to know some stuff about them and all I can find is info on delta F508.
If you know where I can get some info I would greatly appreciate it<img src="i/expressions/face-icon-small-smile.gif" border="0">

Thanks
Stephanie
Mom of 14 yr old son w/ CF
 

steffer73

New member
Hey there,
I have a 14 yr old son w/ CF and he has had a pretty hard time the past 3 yrs. We have been sent to get the double lung evaluation. We have started the prelim. tests to find out where he stands, but I was just told his genotypes (R560T/621+1G).....AND I can't find any info!!! I just want to know some stuff about them and all I can find is info on delta F508.
If you know where I can get some info I would greatly appreciate it<img src="i/expressions/face-icon-small-smile.gif" border="0">

Thanks
Stephanie
Mom of 14 yr old son w/ CF
 

steffer73

New member
Hey there,
I have a 14 yr old son w/ CF and he has had a pretty hard time the past 3 yrs. We have been sent to get the double lung evaluation. We have started the prelim. tests to find out where he stands, but I was just told his genotypes (R560T/621+1G).....AND I can't find any info!!! I just want to know some stuff about them and all I can find is info on delta F508.
If you know where I can get some info I would greatly appreciate it<img src="i/expressions/face-icon-small-smile.gif" border="0">

Thanks
Stephanie
Mom of 14 yr old son w/ CF
 
M

Mommafirst

Guest
I did a quick search. I didn't find any that articles that discuss both, but only looked quickly. Here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=280">R560T</a>


and here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=112">621+1G</a>

with both you can click on the click here at the bottom to see any current pubmed articles on the mutation.

Hope this helps.
 
M

Mommafirst

Guest
I did a quick search. I didn't find any that articles that discuss both, but only looked quickly. Here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=280">R560T</a>


and here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=112">621+1G</a>

with both you can click on the click here at the bottom to see any current pubmed articles on the mutation.

Hope this helps.
 
M

Mommafirst

Guest
I did a quick search. I didn't find any that articles that discuss both, but only looked quickly. Here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=280">R560T</a>


and here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=112">621+1G</a>

with both you can click on the click here at the bottom to see any current pubmed articles on the mutation.

Hope this helps.
 
M

Mommafirst

Guest
I did a quick search. I didn't find any that articles that discuss both, but only looked quickly. Here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=280">R560T</a>


and here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=112">621+1G</a>

with both you can click on the click here at the bottom to see any current pubmed articles on the mutation.

Hope this helps.
 
M

Mommafirst

Guest
I did a quick search. I didn't find any that articles that discuss both, but only looked quickly. Here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=280">R560T</a>


and here are the results for the <a target=_blank class=ftalternatingbarlinklarge href="http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=112">621+1G</a>

with both you can click on the click here at the bottom to see any current pubmed articles on the mutation.

Hope this helps.
 

steffer73

New member
Thanks for the help<img src="i/expressions/face-icon-small-smile.gif" border="0"> I had gone to those sites, but the "medical talk" had my head swimming...LOL! I just wish they would explain it to me in normal terms or pictures. I know I sound pathetic, but since he was diagnosed before birth, I have had to learn a whole new "language" and I am finally getting tired the more they throw at me. He is my inspiration, so I will continue to look for as much info as possible<img src="i/expressions/face-icon-small-smile.gif" border="0">
Thanks again...You Rock<img src="i/expressions/face-icon-small-smile.gif" border="0">

Stephanie
Mom of 14 yr old son w/ CF
 

steffer73

New member
Thanks for the help<img src="i/expressions/face-icon-small-smile.gif" border="0"> I had gone to those sites, but the "medical talk" had my head swimming...LOL! I just wish they would explain it to me in normal terms or pictures. I know I sound pathetic, but since he was diagnosed before birth, I have had to learn a whole new "language" and I am finally getting tired the more they throw at me. He is my inspiration, so I will continue to look for as much info as possible<img src="i/expressions/face-icon-small-smile.gif" border="0">
Thanks again...You Rock<img src="i/expressions/face-icon-small-smile.gif" border="0">

Stephanie
Mom of 14 yr old son w/ CF
 

steffer73

New member
Thanks for the help<img src="i/expressions/face-icon-small-smile.gif" border="0"> I had gone to those sites, but the "medical talk" had my head swimming...LOL! I just wish they would explain it to me in normal terms or pictures. I know I sound pathetic, but since he was diagnosed before birth, I have had to learn a whole new "language" and I am finally getting tired the more they throw at me. He is my inspiration, so I will continue to look for as much info as possible<img src="i/expressions/face-icon-small-smile.gif" border="0">
Thanks again...You Rock<img src="i/expressions/face-icon-small-smile.gif" border="0">

Stephanie
Mom of 14 yr old son w/ CF
 

steffer73

New member
Thanks for the help<img src="i/expressions/face-icon-small-smile.gif" border="0"> I had gone to those sites, but the "medical talk" had my head swimming...LOL! I just wish they would explain it to me in normal terms or pictures. I know I sound pathetic, but since he was diagnosed before birth, I have had to learn a whole new "language" and I am finally getting tired the more they throw at me. He is my inspiration, so I will continue to look for as much info as possible<img src="i/expressions/face-icon-small-smile.gif" border="0">
Thanks again...You Rock<img src="i/expressions/face-icon-small-smile.gif" border="0">

Stephanie
Mom of 14 yr old son w/ CF
 

steffer73

New member
Thanks for the help<img src="i/expressions/face-icon-small-smile.gif" border="0"> I had gone to those sites, but the "medical talk" had my head swimming...LOL! I just wish they would explain it to me in normal terms or pictures. I know I sound pathetic, but since he was diagnosed before birth, I have had to learn a whole new "language" and I am finally getting tired the more they throw at me. He is my inspiration, so I will continue to look for as much info as possible<img src="i/expressions/face-icon-small-smile.gif" border="0">
Thanks again...You Rock<img src="i/expressions/face-icon-small-smile.gif" border="0">

Stephanie
Mom of 14 yr old son w/ CF
 

CFHockeyMom

New member
Both are in the top 10 most common CF genes and both splicing genes which are Classs I genes which means they result in total deficiency or unstable/non-functional CFTR protein.

Allie posted this a while ago...

<div class="FTQUOTE"><begin quote>Genotype-phenotype correlation for pulmonary function in cystic fibrosis.de Gracia J, Mata F, Alvarez A, Casals T, Gatner S, Vendrell M, de la Rosa D, Guarner L, Hermosilla E.
Department of Pneumology, Hospital general Vall d'Hebron, Barcelona, Spain. jgracia@separ.es

BACKGROUND: Since the CFTR gene was cloned, more than 1000 mutations have been identified. To date, a clear relationship has not been established between genotype and the progression of lung damage. A study was undertaken of the relationship between genotype, progression of lung disease, and survival in adult patients with cystic fibrosis (CF). METHODS: A prospective cohort of adult patients with CF and two CFTR mutations followed up in an adult cystic fibrosis unit was analysed. Patients were classified according to functional effects of classes of CFTR mutations and were grouped based on the CFTR molecular position on the epithelial cell surface (I-II/I-II, I-II/III-V). Spirometric values, progression of lung disease, probability of survival, and clinical characteristics were analysed between groups. RESULTS: Seventy four patients were included in the study. Patients with genotype I-II/I-II had significantly lower current spirometric values (p < 0.001), greater loss of pulmonary function (p < 0.04), a higher proportion of end-stage lung disease (p < 0.001), a higher risk of suffering from moderate to severe lung disease (odds ratio 7.12 (95% CI 1.3 to 40.5)) and a lower probability of survival than patients with genotype I-II/III, I-II/IV and I-II/V (p < 0.001). CONCLUSIONS: The presence of class I or II mutations on both chromosomes is associated with worse respiratory disease and a lower probability of survival.</end quote></div>

Specific gene types/classes don't guarantee the severity of the disease or the progression however, the info can be referred to as a "rule of thumb". Environment, treatment quality, and treatment compliance are equally important in determining long term prognosis.
 

CFHockeyMom

New member
Both are in the top 10 most common CF genes and both splicing genes which are Classs I genes which means they result in total deficiency or unstable/non-functional CFTR protein.

Allie posted this a while ago...

<div class="FTQUOTE"><begin quote>Genotype-phenotype correlation for pulmonary function in cystic fibrosis.de Gracia J, Mata F, Alvarez A, Casals T, Gatner S, Vendrell M, de la Rosa D, Guarner L, Hermosilla E.
Department of Pneumology, Hospital general Vall d'Hebron, Barcelona, Spain. jgracia@separ.es

BACKGROUND: Since the CFTR gene was cloned, more than 1000 mutations have been identified. To date, a clear relationship has not been established between genotype and the progression of lung damage. A study was undertaken of the relationship between genotype, progression of lung disease, and survival in adult patients with cystic fibrosis (CF). METHODS: A prospective cohort of adult patients with CF and two CFTR mutations followed up in an adult cystic fibrosis unit was analysed. Patients were classified according to functional effects of classes of CFTR mutations and were grouped based on the CFTR molecular position on the epithelial cell surface (I-II/I-II, I-II/III-V). Spirometric values, progression of lung disease, probability of survival, and clinical characteristics were analysed between groups. RESULTS: Seventy four patients were included in the study. Patients with genotype I-II/I-II had significantly lower current spirometric values (p < 0.001), greater loss of pulmonary function (p < 0.04), a higher proportion of end-stage lung disease (p < 0.001), a higher risk of suffering from moderate to severe lung disease (odds ratio 7.12 (95% CI 1.3 to 40.5)) and a lower probability of survival than patients with genotype I-II/III, I-II/IV and I-II/V (p < 0.001). CONCLUSIONS: The presence of class I or II mutations on both chromosomes is associated with worse respiratory disease and a lower probability of survival.</end quote></div>

Specific gene types/classes don't guarantee the severity of the disease or the progression however, the info can be referred to as a "rule of thumb". Environment, treatment quality, and treatment compliance are equally important in determining long term prognosis.
 

CFHockeyMom

New member
Both are in the top 10 most common CF genes and both splicing genes which are Classs I genes which means they result in total deficiency or unstable/non-functional CFTR protein.

Allie posted this a while ago...

<div class="FTQUOTE"><begin quote>Genotype-phenotype correlation for pulmonary function in cystic fibrosis.de Gracia J, Mata F, Alvarez A, Casals T, Gatner S, Vendrell M, de la Rosa D, Guarner L, Hermosilla E.
Department of Pneumology, Hospital general Vall d'Hebron, Barcelona, Spain. jgracia@separ.es

BACKGROUND: Since the CFTR gene was cloned, more than 1000 mutations have been identified. To date, a clear relationship has not been established between genotype and the progression of lung damage. A study was undertaken of the relationship between genotype, progression of lung disease, and survival in adult patients with cystic fibrosis (CF). METHODS: A prospective cohort of adult patients with CF and two CFTR mutations followed up in an adult cystic fibrosis unit was analysed. Patients were classified according to functional effects of classes of CFTR mutations and were grouped based on the CFTR molecular position on the epithelial cell surface (I-II/I-II, I-II/III-V). Spirometric values, progression of lung disease, probability of survival, and clinical characteristics were analysed between groups. RESULTS: Seventy four patients were included in the study. Patients with genotype I-II/I-II had significantly lower current spirometric values (p < 0.001), greater loss of pulmonary function (p < 0.04), a higher proportion of end-stage lung disease (p < 0.001), a higher risk of suffering from moderate to severe lung disease (odds ratio 7.12 (95% CI 1.3 to 40.5)) and a lower probability of survival than patients with genotype I-II/III, I-II/IV and I-II/V (p < 0.001). CONCLUSIONS: The presence of class I or II mutations on both chromosomes is associated with worse respiratory disease and a lower probability of survival.</end quote></div>

Specific gene types/classes don't guarantee the severity of the disease or the progression however, the info can be referred to as a "rule of thumb". Environment, treatment quality, and treatment compliance are equally important in determining long term prognosis.
 

CFHockeyMom

New member
Both are in the top 10 most common CF genes and both splicing genes which are Classs I genes which means they result in total deficiency or unstable/non-functional CFTR protein.

Allie posted this a while ago...

<div class="FTQUOTE"><begin quote>Genotype-phenotype correlation for pulmonary function in cystic fibrosis.de Gracia J, Mata F, Alvarez A, Casals T, Gatner S, Vendrell M, de la Rosa D, Guarner L, Hermosilla E.
Department of Pneumology, Hospital general Vall d'Hebron, Barcelona, Spain. jgracia@separ.es

BACKGROUND: Since the CFTR gene was cloned, more than 1000 mutations have been identified. To date, a clear relationship has not been established between genotype and the progression of lung damage. A study was undertaken of the relationship between genotype, progression of lung disease, and survival in adult patients with cystic fibrosis (CF). METHODS: A prospective cohort of adult patients with CF and two CFTR mutations followed up in an adult cystic fibrosis unit was analysed. Patients were classified according to functional effects of classes of CFTR mutations and were grouped based on the CFTR molecular position on the epithelial cell surface (I-II/I-II, I-II/III-V). Spirometric values, progression of lung disease, probability of survival, and clinical characteristics were analysed between groups. RESULTS: Seventy four patients were included in the study. Patients with genotype I-II/I-II had significantly lower current spirometric values (p < 0.001), greater loss of pulmonary function (p < 0.04), a higher proportion of end-stage lung disease (p < 0.001), a higher risk of suffering from moderate to severe lung disease (odds ratio 7.12 (95% CI 1.3 to 40.5)) and a lower probability of survival than patients with genotype I-II/III, I-II/IV and I-II/V (p < 0.001). CONCLUSIONS: The presence of class I or II mutations on both chromosomes is associated with worse respiratory disease and a lower probability of survival.</end quote>

Specific gene types/classes don't guarantee the severity of the disease or the progression however, the info can be referred to as a "rule of thumb". Environment, treatment quality, and treatment compliance are equally important in determining long term prognosis.
 

CFHockeyMom

New member
Both are in the top 10 most common CF genes and both splicing genes which are Classs I genes which means they result in total deficiency or unstable/non-functional CFTR protein.

Allie posted this a while ago...

<div class="FTQUOTE"><begin quote>Genotype-phenotype correlation for pulmonary function in cystic fibrosis.de Gracia J, Mata F, Alvarez A, Casals T, Gatner S, Vendrell M, de la Rosa D, Guarner L, Hermosilla E.
Department of Pneumology, Hospital general Vall d'Hebron, Barcelona, Spain. jgracia@separ.es

BACKGROUND: Since the CFTR gene was cloned, more than 1000 mutations have been identified. To date, a clear relationship has not been established between genotype and the progression of lung damage. A study was undertaken of the relationship between genotype, progression of lung disease, and survival in adult patients with cystic fibrosis (CF). METHODS: A prospective cohort of adult patients with CF and two CFTR mutations followed up in an adult cystic fibrosis unit was analysed. Patients were classified according to functional effects of classes of CFTR mutations and were grouped based on the CFTR molecular position on the epithelial cell surface (I-II/I-II, I-II/III-V). Spirometric values, progression of lung disease, probability of survival, and clinical characteristics were analysed between groups. RESULTS: Seventy four patients were included in the study. Patients with genotype I-II/I-II had significantly lower current spirometric values (p < 0.001), greater loss of pulmonary function (p < 0.04), a higher proportion of end-stage lung disease (p < 0.001), a higher risk of suffering from moderate to severe lung disease (odds ratio 7.12 (95% CI 1.3 to 40.5)) and a lower probability of survival than patients with genotype I-II/III, I-II/IV and I-II/V (p < 0.001). CONCLUSIONS: The presence of class I or II mutations on both chromosomes is associated with worse respiratory disease and a lower probability of survival.</end quote>

Specific gene types/classes don't guarantee the severity of the disease or the progression however, the info can be referred to as a "rule of thumb". Environment, treatment quality, and treatment compliance are equally important in determining long term prognosis.
 
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