Cystic fibrosis

[Guest guest]

All three of mine have been tested - I sort of assumed it was standard

protocol.

Dayna

Cystic Fibrosis

Hi!

Have any of your children ever been tested for Cystic Fibrosis?

is being sent for a sweat test to rule out CF. I don't see

that it's a possibility although I agree that he meets the

qualifications of being tested (frequent upper respiratory illnesses,

chronic greasy diarrhea, slowed growth/weight gain).

All of these could be related to his mild immune deficiency, so I'm

not too worried -- just would rather not have to deal with the stress

of thinking that Cystic Fibrosis is a possibility (however small of a

possibility).

I was just curious if any of your kids have been tested for it

Thanks,

Connie (Mommy to - 19 months old with low IgG)

This forum is open to parents and caregivers of children diagnosed with

a Primary Immune Deficiency. Opinions or medical advice stated here are

the sole responsibility of the poster and should not be taken as

professional advice.

To unsubscribe -unsubscribegroups (DOT)

To search group archives go to:

/messages

[Guest guest]

was tested at 2 months because of his failure to thrive. It was

negative. But, he sure sweats a lot when he sleeps, so it is something

that I'm going to mention next week to the immuno.

, 2yo, cyclic neutropenia, IgG deficiency with sub class 3

deficiency, Secretory IgA deficient, Low T cells, Low C4, Iron

deficiency anemia (resolved)

igh, 4 3/4, Mild CP, Chronic ear and sinus infections IgE deficient.

Libby, 10 y/o, healthy who loves playing basketball and tap dancing.

Kaitlyn, 13 y/o, mild asthma, otherwise healthy with a typical 13 going

on 30 attitude.....

Warren, husband of 6 years, IDDM using an insulin pump at present.

Cystic Fibrosis

Hi!

Have any of your children ever been tested for Cystic Fibrosis?

is being sent for a sweat test to rule out CF. I don't see

that it's a possibility although I agree that he meets the

qualifications of being tested (frequent upper respiratory illnesses,

chronic greasy diarrhea, slowed growth/weight gain).

All of these could be related to his mild immune deficiency, so I'm

not too worried -- just would rather not have to deal with the stress

of thinking that Cystic Fibrosis is a possibility (however small of a

possibility).

I was just curious if any of your kids have been tested for it

Thanks,

Connie (Mommy to - 19 months old with low IgG)

This forum is open to parents and caregivers of children diagnosed with

a Primary Immune Deficiency. Opinions or medical advice stated here are

the sole responsibility of the poster and should not be taken as

professional advice.

To unsubscribe -unsubscribegroups (DOT)

To search group archives go to:

/messages

[Guest guest]

Connor was tested for CF as well, I think when he was about 15 months

old. As I recall, it was one of the early tests we had done--of

course they want to rule out something like this early on (or,

alternately, diagnose it early to get proper treatment).

, mom of (5 y.o. ballet school dropout) and Connor (3 y.

o. currently chewing on my bedspread, hyper IgM, PDD-NOS)

>

> Hi!

>

> Have any of your children ever been tested for Cystic Fibrosis?

> is being sent for a sweat test to rule out CF. I don't see

> that it's a possibility although I agree that he meets the

> qualifications of being tested (frequent upper respiratory

illnesses,

> chronic greasy diarrhea, slowed growth/weight gain).

>

> All of these could be related to his mild immune deficiency, so I'm

> not too worried -- just would rather not have to deal with the

stress

> of thinking that Cystic Fibrosis is a possibility (however small of

a

> possibility).

>

> I was just curious if any of your kids have been tested for it

>

> Thanks,

> Connie (Mommy to - 19 months old with low IgG)

[Guest guest]

Connie,

has been tested twice for CF. Actually, 2 sweat tests, both neg, and

DNA testing, she came back with one mutation, you need 2 for a definitive

diagnosis. the pulmonologist said he can't totally rule it out because they only

test for 77 mutations and there may be more. I try not to worry about it, the

PID is bad enough.

, mom to - CVID, asthma, GERD

Cystic Fibrosis

Hi!

Have any of your children ever been tested for Cystic Fibrosis?

is being sent for a sweat test to rule out CF. I don't see

that it's a possibility although I agree that he meets the

qualifications of being tested (frequent upper respiratory illnesses,

chronic greasy diarrhea, slowed growth/weight gain).

All of these could be related to his mild immune deficiency, so I'm

not too worried -- just would rather not have to deal with the stress

of thinking that Cystic Fibrosis is a possibility (however small of a

possibility).

I was just curious if any of your kids have been tested for it

Thanks,

Connie (Mommy to - 19 months old with low IgG)

This forum is open to parents and caregivers of children diagnosed with a

Primary Immune Deficiency. Opinions or medical advice stated here are the sole

responsibility of the poster and should not be taken as professional advice.

To unsubscribe

-unsubscribe@groups<mailto:-unsubscribe@groups>.

To search group archives go to:

/messages<PedP\

ID/messages>

[Guest guest]

has been tested twice for CF. Both times negative. It is one of the

easier tests we have ever had to go thru.

Amy, mom to:

, 21 months old. CVID, MSPI, GERD, Asthma.. On claritin, flovent,

xopenex, and IVIG sub Q every two weeks (Carimune NF)

visit Nick's website:

http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.org/ne/nicho\

lasb/>

Cystic Fibrosis

Hi!

Have any of your children ever been tested for Cystic Fibrosis?

is being sent for a sweat test to rule out CF. I don't see

that it's a possibility although I agree that he meets the

qualifications of being tested (frequent upper respiratory illnesses,

chronic greasy diarrhea, slowed growth/weight gain).

All of these could be related to his mild immune deficiency, so I'm

not too worried -- just would rather not have to deal with the stress

of thinking that Cystic Fibrosis is a possibility (however small of a

possibility).

I was just curious if any of your kids have been tested for it

Thanks,

Connie (Mommy to - 19 months old with low IgG)

This forum is open to parents and caregivers of children diagnosed with a

Primary Immune Deficiency. Opinions or medical advice stated here are the sole

responsibility of the poster and should not be taken as professional advice.

To unsubscribe -unsubscribegroups (DOT)

To search group archives go to:

/messages<PedP\

ID/messages>

[Guest guest]

-Hi I just wanted to ask why did they test your son twice for CF? We

were told that once our daughter was tested for CF that they rule

that out and she would not ever need to be tested again.

-- In , " Amy Bolich " <amyjo4181@m...> wrote:

> has been tested twice for CF. Both times negative. It is

one of the easier tests we have ever had to go thru.

>

> Amy, mom to:

> , 21 months old. CVID, MSPI, GERD, Asthma.. On claritin,

flovent, xopenex, and IVIG sub Q every two weeks (Carimune NF)

>

> visit Nick's website:

http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.or

g/ne/nicholasb/>

> Cystic Fibrosis

>

>

>

> Hi!

>

> Have any of your children ever been tested for Cystic Fibrosis?

> is being sent for a sweat test to rule out CF. I don't

see

> that it's a possibility although I agree that he meets the

> qualifications of being tested (frequent upper respiratory

illnesses,

> chronic greasy diarrhea, slowed growth/weight gain).

>

> All of these could be related to his mild immune deficiency, so

I'm

> not too worried -- just would rather not have to deal with the

stress

> of thinking that Cystic Fibrosis is a possibility (however small

of a

> possibility).

>

> I was just curious if any of your kids have been tested for it

>

> Thanks,

> Connie (Mommy to - 19 months old with low IgG)

>

>

>

>

>

> This forum is open to parents and caregivers of children

diagnosed with a Primary Immune Deficiency. Opinions or medical

advice stated here are the sole responsibility of the poster and

should not be taken as professional advice.

>

> To unsubscribe -unsubscribegroups (DOT)

> To search group archives go to:

/messages<

group//messages>

>

>

>

[Guest guest]

They did the test when he was 5months old and then he had a bronchoscopy that

showed sever redness and mucous in the lungs so they repeated it at 6 months to

be sure since the scope showed what looked like CF. We still don't know what

causes the build up of mucous in his lungs, they thought maybe a cilliary

disfunction, the little hairs that are in the lungs that are supposed to push

the mucous out. We haven't tested for it yet. And to be honest since starting

the Sub Q he hasn't had many problems with the rattling in his chest.

Amy, mom to:

, 21 months old. CVID, MSPI, GERD, Asthma.. On claritin, flovent,

xopenex, and IVIG sub Q every two weeks (Carimune NF)

visit Nick's website:

http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.org/ne/nicho\

lasb/>

Cystic Fibrosis

>

>

>

> Hi!

>

> Have any of your children ever been tested for Cystic Fibrosis?

> is being sent for a sweat test to rule out CF. I don't

see

> that it's a possibility although I agree that he meets the

> qualifications of being tested (frequent upper respiratory

illnesses,

> chronic greasy diarrhea, slowed growth/weight gain).

>

> All of these could be related to his mild immune deficiency, so

I'm

> not too worried -- just would rather not have to deal with the

stress

> of thinking that Cystic Fibrosis is a possibility (however small

of a

> possibility).

>

> I was just curious if any of your kids have been tested for it

>

> Thanks,

> Connie (Mommy to - 19 months old with low IgG)

>

>

>

>

>

> This forum is open to parents and caregivers of children

diagnosed with a Primary Immune Deficiency. Opinions or medical

advice stated here are the sole responsibility of the poster and

should not be taken as professional advice.

>

> To unsubscribe -unsubscribegroups (DOT)

> To search group archives go to:

/messages<PedP\

ID/messages><<>

group//messages>

>

>

>

[Guest guest]

Hi,

My daughter was also tested for cystic fibrosis by her

pulmonologist. It is a standard test that they do as soon as they

see characteristic symptoms. It didn't hurt at all there were no

injections or anything, they just apply heat or electric stimulation

and make the child's hands sweat, then test the sweat that was

collected and see if it is positive for cystic fibrosis. The test

took less than an hour, we went on a weekday and the doctor called

ahead so it was really not even a long wait at the children's

hospital. She was negative.

I make sure I get copies of all her hospital and test records and

when we went to her current specialist I gave him a copy of the

results of the cystic fibrosis test, so they are on her chart. There

is no need to test more than once for cystic fibrosis, from what I

was told by the doctors. So I have copies of the results and the

information from the hospital where she took the test (which is the

best one in our area for that test) and when the doctors say, " has

she been tested for cystic fibrosis? " I say, " yes, she was negative "

and I fax over or hand them the results and they don't require

another test they just put the results in her file/on her chart.

Please dont' worry too much about the test. My daughter was a little

freaked out by it, due to the fact that we were in a hospital and

there was this strange man in a white coat doing funny things to her

hands, and not sure what the electrical stuff was about but it was

not a big shock or jolt or anything at all, just a warm tingle like

when you shave with an electric shaver, and it was over in less than

10 minutes and she was fine, not a tear was shed. It didn't hurt, it

really didnt'. I would say it did if it did. No injections, she was

fine. We stayed there in the room with her, both me and my husband,

while the test was administered, and we talked to her and asked what

she was feeling and stuff and she was ok.

It is important to know if there is cystic fibrosis because early

detection of this particular illness is key. But they test only to

rule it out, it is standard procedure, once it is ruled out they move

on to other things, which in our case was checking her

immunoglobulins, and that was a more traumatic thing because my

daughter hates the needles, hates to give blood, screams and kicks

and demands to go home, and we have to hold her down. If your child

has PID this is truly the mildest test the child will probably deal

with. Please don't worry, it will be ok. Explain to the child what

to expect and that might help. It won't hurt. I had him buzz me

with the test node before he tested my daughter, and it really didn't

hurt at all.

[Guest guest]

there you are I was wondering when you'd post up...

For my friends in the group, is my husband.

Yeah I remember the doctor saying once she was tested she never had

to retest so I was confused by this too. We have to fax the CF test

results to the pulmonologist - please remind me to do that.

/Day

> > has been tested twice for CF. Both times negative. It

is

> one of the easier tests we have ever had to go thru.

> >

> > Amy, mom to:

> > , 21 months old. CVID, MSPI, GERD, Asthma.. On claritin,

> flovent, xopenex, and IVIG sub Q every two weeks (Carimune NF)

> >

> > visit Nick's website:

>

http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.or

> g/ne/nicholasb/>

> > Cystic Fibrosis

> >

> >

> >

> > Hi!

> >

> > Have any of your children ever been tested for Cystic

Fibrosis?

> > is being sent for a sweat test to rule out CF. I don't

> see

> > that it's a possibility although I agree that he meets the

> > qualifications of being tested (frequent upper respiratory

> illnesses,

> > chronic greasy diarrhea, slowed growth/weight gain).

> >

> > All of these could be related to his mild immune deficiency, so

> I'm

> > not too worried -- just would rather not have to deal with the

> stress

> > of thinking that Cystic Fibrosis is a possibility (however

small

> of a

> > possibility).

> >

> > I was just curious if any of your kids have been tested for it

> >

> > Thanks,

> > Connie (Mommy to - 19 months old with low IgG)

> >

> >

> >

> >

> >

> > This forum is open to parents and caregivers of children

> diagnosed with a Primary Immune Deficiency. Opinions or medical

> advice stated here are the sole responsibility of the poster and

> should not be taken as professional advice.

> >

> > To unsubscribe -unsubscribegroups (DOT)

> > To search group archives go to:

>

/messages<

> group//messages>

> >

> >

> >

[Guest guest]

Hi Sue,

I did, someone on one of my cf support groups mentioned it. I believe they are passing a law here in CA doing the same. They will use the same spot of blood as they use for PKU and all the other testing. Those of us in the cf community are pleased as it is best if babies with cf are diagnosed early and treatment is started ASAP. It sure would have saved us a lot of grief, my daughter was quite ill for two months before she was dxed.

love,

[Guest guest]

i have not heard this but definately will check into it. being that i live in ohio i think that this is wonderful. i think the key thing in cystic fibrosis is treatment and proper treatment. an earlier diagnosis can mean proper ontime treatment. evelynSue <sweetsueohio2002@...> wrote: I just heard on the news, as of now ALL newborns in Ohio HAVE to be tested for Cystic Fibrosis at birth. Did anyone else hear anything about this? Sue For a REALLY HOT time check out http://www.peternoone.com and http://www.mikesmith1964.com

How low will we go? Check out Messenger’s low PC-to-Phone call rates.

[Guest guest]

While I totally agree with what you are saying about early diagnosis leading to earlier treatment, doesn't this also give medical insurance companies fuel to deny more people the right to insurance due to " pre-existing conditions " ? Please correct me if I'm wrong; I don't know much about how health insurance works because I don't go through regular insurance for my healthcare.

On 8/29/06, evelyn <peaches0106@...> wrote:

i have not heard this but definately will check into it. being that i live in ohio i think that this is wonderful. i think the key thing in cystic fibrosis is treatment and proper treatment. an earlier diagnosis can mean proper ontime treatment.

evelynSue <sweetsueohio2002 > wrote:

I just heard on the news, as of now ALL newborns in Ohio HAVE to be tested for Cystic Fibrosis at birth. Did anyone else hear anything about this? Sue

For a REALLY HOT time check out http://www.peternoone.com and

http://www.mikesmit

h1964.com How low will we go? Check out Messenger's low

PC-to-Phone call rates.

-- Tracey White (tracey.white@...)Life Partner to Piskur (Commitment Ceremony: 8/5/00) " They go dancing, around and around, without any cares; and her very first true love is holding her close; and for a moment, she isn't scared. " - Skin (Sarabeth) by Rascal Flatts

[Guest guest]

There was a new law passed (not sure if it is just my state or nationwide) that it is illegal to discriminate based on genetics, or the result of genetic testing. However...that still isn't enough for me to be covered for my diabetes supplies. I don't fully understand the law yet, I've been looking for a good explaination of it. I hope this is the start to making it illegal for insurance companies to deny anyone for any condition.

-----Original Message-----From: [mailto: ] On Behalf Of Tracey WhiteSent: Tuesday, August 29, 2006 9:14 PM Subject: Re: Cystic Fibrosis

While I totally agree with what you are saying about early diagnosis leading to earlier treatment, doesn't this also give medical insurance companies fuel to deny more people the right to insurance due to "pre-existing conditions"? Please correct me if I'm wrong; I don't know much about how health insurance works because I don't go through regular insurance for my healthcare.

On 8/29/06, evelyn <peaches0106 > wrote:

i have not heard this but definately will check into it. being that i live in ohio i think that this is wonderful. i think the key thing in cystic fibrosis is treatment and proper treatment. an earlier diagnosis can mean proper ontime treatment.

evelynSue <sweetsueohio2002 > wrote:

I just heard on the news, as of now ALL newborns in Ohio HAVE to be tested for Cystic Fibrosis at birth. Did anyone else hear anything about this?

Sue

For a REALLY HOT time check out http://www.peternoone.com and

http://www.mikesmit h1964.com

How low will we go? Check out Messenger's low PC-to-Phone call rates.

-- Tracey White (tracey.whitegmail)Life Partner to Piskur (Commitment Ceremony: 8/5/00) "They go dancing, around and around, without any cares; and her very first true love is holding her close; and for a moment, she isn't scared." - Skin (Sarabeth) by Rascal Flatts

[Guest guest]

hi, my name is evelyn and my son has cystic fibrosis. i sure do hope you are feeling better soon. keep us posted on how you are doing. evelynIsabell <qwerty_shy_strawberry06@...> wrote: Hey...I am liz... I have CF and i was diagnosed when i was six years old... I also have 8 other illness's but not as serious...i am currently not on any treatments but i got sick on christmas and i still am sick.... I been puking up mucus, coughing, wheezing, gasping for

air... ect.... i am slowly getting better __________________________________________________

[Guest guest]

I got worse today....I am wheezing.. alot more.... mucus.....I'm having a real hard time breathingevelyn <peaches0106@...> wrote: hi, my name is evelyn and my son has cystic fibrosis. i sure do hope you are feeling better soon. keep us posted on how you are doing. evelynIsabell <qwerty_shy_strawberry06 > wrote: Hey...I am liz... I have CF and i was diagnosed when i was six years old... I also have 8 other illness's but not as serious...i am currently not on any treatments but i got sick on christmas and i still am sick.... I been puking up mucus, coughing, wheezing, gasping for air... ect.... i am slowly getting better __________________________________________________

[Guest guest]

I got worse today....I am wheezing.. alot more.... mucus.....I'm having a real hard time breathingevelyn <peaches0106@...> wrote: hi, my name is evelyn and my son has cystic fibrosis. i sure do hope you are feeling better soon. keep us posted on how you are doing. evelynIsabell <qwerty_shy_strawberry06 > wrote: Hey...I am liz... I have CF and i was diagnosed when i was six years old... I also have 8 other illness's but not as serious...i am currently not on any treatments but i got sick on christmas and i still am sick.... I been puking up mucus, coughing, wheezing, gasping for air... ect.... i am slowly getting better __________________________________________________

[Guest guest]

Hi Liz and ,

My daughter has Cf and Down syndrome. We are doing great right now and just trying to recover from the Christmas holidays. Welcome to our group and feel free to ask questions or jump in anytime.

Peace and Blessings,

Dinkins-Borkowski; Nolan(4) nocf, Phoebe(2) Ds & Cf

Phoebe's Video: http://www.active.com/donate/buddywalk2006/phight4phoebe

Get Phoebe-Chic: http://www.cafepress.com/phoebesphight

Re: cystic fibrosis

hi, my name is evelyn and my son has cystic fibrosis. i sure do hope you are feeling better soon. keep us posted on how you are doing.

evelynIsabell <qwerty_shy_strawber ry06 (DOT) com> wrote:

Hey...I am liz... I have CF and i was diagnosed when i was six years old... I also have 8 other illness's but not as serious...i am currently not on any treatments but i got sick on christmas and i still am sick.... I been puking up mucus, coughing, wheezing, gasping for air... ect.... i am slowly getting better

____________ _________ _________ _________ _________ __

[Guest guest]

I am sorry that your faughter has CF....but I am glad thingswere doing good for you....things are not so hot with me right now...I'm having alot of breathing problems and i am coughing up alot of mucus Borkowski <julieborkowski@...> wrote: Hi Liz and , My daughter has Cf and Down syndrome. We are doing great right now and just trying to recover from the Christmas

holidays. Welcome to our group and feel free to ask questions or jump in anytime. Peace and Blessings, Dinkins-Borkowski; Nolan(4) nocf, Phoebe(2) Ds & Cf Phoebe's Video: http://www.active.com/donate/buddywalk2006/phight4phoebe Get Phoebe-Chic: http://www.cafepress.com/phoebesphight Re: cystic fibrosis hi, my name is evelyn and my son has cystic fibrosis. i sure do hope you are feeling better soon. keep us posted on how you are doing. evelynIsabell <qwerty_shy_strawber ry06 (DOT) com> wrote: Hey...I am liz... I have CF and i was diagnosed when i was six years old... I also have 8 other illness's but not as

serious...i am currently not on any treatments but i got sick on christmas and i still am sick.... I been puking up mucus, coughing, wheezing, gasping for air... ect.... i am slowly getting better ____________ _________ _________ _________ _________ __

[Guest guest]

hi julie. i think i have seen you on cf parents to. i have seen phoebes sight before. drop me a line some time. evelyn Borkowski <julieborkowski@...> wrote: Hi Liz and , My daughter has Cf and Down syndrome. We are doing great right now and just trying to recover from the Christmas holidays. Welcome to our

group and feel free to ask questions or jump in anytime. Peace and Blessings, Dinkins-Borkowski; Nolan(4) nocf, Phoebe(2) Ds & Cf Phoebe's Video: http://www.active.com/donate/buddywalk2006/phight4phoebe Get Phoebe-Chic: http://www.cafepress.com/phoebesphight Re: cystic fibrosis hi, my name is evelyn and my son has cystic fibrosis. i sure do hope you are feeling better soon. keep us posted on how you are doing. evelynIsabell <qwerty_shy_strawber ry06 (DOT) com> wrote: Hey...I am liz... I have CF and i was diagnosed when i was six years old... I also have 8 other illness's but not as serious...i am currently not on any treatments but i got sick on

christmas and i still am sick.... I been puking up mucus, coughing, wheezing, gasping for air... ect.... i am slowly getting better ____________ _________ _________ _________ _________ __

[Guest guest]

Do you have a vest?

Dinkins-Borkowski; Nolan(4) nocf, Phoebe(2) Ds & Cf

Phoebe's Video: http://www.active.com/donate/buddywalk2006/phight4phoebe

Get Phoebe-Chic: http://www.cafepress.com/phoebesphight

Re: cystic fibrosis

hi, my name is evelyn and my son has cystic fibrosis. i sure do hope you are feeling better soon. keep us posted on how you are doing.

evelynIsabell <qwerty_shy_strawber ry06 (DOT) com> wrote:

Hey...I am liz... I have CF and i was diagnosed when i was six years old... I also have 8 other illness's but not as serious...i am currently not on any treatments but i got sick on christmas and i still am sick.... I been puking up mucus, coughing, wheezing, gasping for air... ect.... i am slowly getting better

____________ _________ _________ _________ _________ __

[Guest guest]

No I do not.... Borkowski <julieborkowski@...> wrote: Do you have a vest? Dinkins-Borkowski; Nolan(4) nocf, Phoebe(2) Ds & Cf Phoebe's Video: http://www.active.com/donate/buddywalk2006/phight4phoebe Get Phoebe-Chic: http://www.cafepress.com/phoebesphight Re: cystic fibrosis hi, my name is evelyn and my son has cystic fibrosis. i sure do hope you are feeling better soon. keep us posted on how you are doing. evelynIsabell <qwerty_shy_strawber ry06 (DOT) com> wrote: Hey...I am liz... I have CF and i was diagnosed when i was six years old... I also have 8 other illness's but not as serious...i am currently not on any treatments but i got sick on christmas and i still am sick.... I been puking up mucus, coughing, wheezing, gasping for air... ect.... i am slowly getting better ____________ _________ _________ _________ _________

__

[Guest guest]

Plz help in this Q

Oral manifestation of cystic fibrosis include all the following except

A tend to be mouth breathers

B salivary gland enlarge

C increase in dental caries

D increase in calculus deposits

E Intrinsic teeth staining due to tetracycline

Thanks

Sent from my iPad

[Guest guest]

may be increase in calculus not present because in scully they said may they have xerostomia From: Balsam_Majid <balsam_majid@...> " " < > Sent: Saturday, April

14, 2012 10:45 AM Subject: Cystic fibrosis

Plz help in this Q

Oral manifestation of cystic fibrosis include all the following except

A tend to be mouth breathers

B salivary gland enlarge

C increase in dental caries

D increase in calculus deposits

E Intrinsic teeth staining due to tetracycline

Thanks

Sent from my iPad

[Guest guest]

Yes I agreeSent from my iPadOn 14 Apr 2012, at 09:59, Farah Hasan <farahghassanhasan@...> wrote:

may be increase in calculus not present because in scully they said may they have xerostomia From: Balsam_Majid <balsam_majid@...> " " < > Sent: Saturday, April

14, 2012 10:45 AM Subject: Cystic fibrosis

Plz help in this Q

Oral manifestation of cystic fibrosis include all the following except

A tend to be mouth breathers

B salivary gland enlarge

C increase in dental caries

D increase in calculus deposits

E Intrinsic teeth staining due to tetracycline

Thanks

Sent from my iPad