Customize Consent Preferences

We use cookies to help you navigate efficiently and perform certain functions. You will find detailed information about all cookies under each consent category below.

The cookies that are categorized as "Necessary" are stored on your browser as they are essential for enabling the basic functionalities of the site. ... 

Always Active

Necessary cookies are required to enable the basic features of this site, such as providing secure log-in or adjusting your consent preferences. These cookies do not store any personally identifiable data.

No cookies to display.

Functional cookies help perform certain functionalities like sharing the content of the website on social media platforms, collecting feedback, and other third-party features.

No cookies to display.

Analytical cookies are used to understand how visitors interact with the website. These cookies help provide information on metrics such as the number of visitors, bounce rate, traffic source, etc.

No cookies to display.

Performance cookies are used to understand and analyze the key performance indexes of the website which helps in delivering a better user experience for the visitors.

No cookies to display.

Advertisement cookies are used to provide visitors with customized advertisements based on the pages you visited previously and to analyze the effectiveness of the ad campaigns.

No cookies to display.

EU-PFF NEWS

When Pulmonary Fibrosis is a hereditary condition

20 Oct 2021 - 09:10

Share this

     

Longfibrose Patiëntenvereniging in the Netherlands has produced an information folder

The folder contains information about familial pulmonary fibrosis – what this is, how it can be diagnosed, and what it means for family members of familial pulmonary fibrosis patients. Most people with pulmonary fibrosis are the only one in their family with the disease. But in about 20% (1 in 5) there are also affected family members. If two or more family members have pulmonary fibrosis, familial pulmonary fibrosis is diagnosed, and there is a need for genetic testing.

Read about the symptoms, needs for genetic testing and regular follow-up if Pulmonary Fibrosis occurs in more family members in the folder, which you can download here.

Related News & Events

New President Elected!

New President Elected!

The European Pulmonary Fibrosis Federation (EU-PFF) is pleased to announce the appointment of John...