Pcd and cystic fybrosis: Hi is it... - PCD Family Suppor...

PCD Family Support Group (UK)

618 members302 posts

Pcd and cystic fybrosis

Chrisjudy profile image
2 Replies

Hi is it possible that my child could have pcd and cystic fibroses becouse his doctor did genetic tests on him and this is what she said is the results.

" His results are positive for primary ciliary dyskinesia, the cystic fibrosis studies are inconclusive and I have asked the geneticist to look at the results again."

Written by
Chrisjudy profile image
Chrisjudy
To view profiles and participate in discussions please or .
2 Replies
fionac66 profile image
fionac66

Hi - I am sorry I don't know enough about CF genetic tests to answer this.

Where are you having the tests done? Here in the UK they don't normally test for PCD with genetic tests as they can only find 70% of PCD cases - it is normally confirmed using nasal brushing analysis.

Whatever the diagnosis is the most important thing is that you start physiotherapy treatment asap to get the secretions moving out of the lungs and treat any chest infection asap with targeted antibiotics.

Good luck!

Fiona

fionac66 profile image
fionac66 in reply tofionac66

Hi - sorry just realised we have been in contact before and that you are in South Africa. If you find out a bit more about the genetic test (e.g. which Gene they think is causing the PCD) I can probably be of more help.

Not what you're looking for?

You may also like...

PCD and Diabetes

Hi, I am currently in hospital due to an exercbation related to my PCD and Bronchietasis. I have...
Rach29 profile image

PCD and IVF Funding

Hello, I was hoping to get some advice from anyone that might be or have been in a similar...
Freddo_8 profile image

Our baby has PCD

Are there any parents on here with babies that have PCD. Olivia is 6 months old We found out she...
Jpeas profile image

Fertility and PCD

Hi are there any mothers here with PCD. I would really appreciate anyone who can talk to me about...
Emily_sa profile image

PCD/Bronchiectasis and headaches

Hi everyone, I have PCD and bronchiectasis and regularly get headaches which stems from my shoulder...
Iram_sa profile image

Moderation team

TerryBun profile image
TerryBunAdministrator
LD28 profile image
LD28Administrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.