15

Is Hereditary Angioedema contagious?

Is Hereditary Angioedema transmitted from person to person? Is Hereditary Angioedema contagious? What are the routes of contagion? People with experience in Hereditary Angioedema help solve this question.

Is Hereditary Angioedema contagious?

Hereditary Angioedema (HAE) is not contagious. It is a rare genetic disorder characterized by recurrent episodes of swelling in various body parts, including the face, hands, feet, and airways. HAE is caused by a deficiency or dysfunction of certain proteins in the blood. It is not transmitted through contact or exposure to affected individuals. HAE is an inherited condition, meaning it is passed down from parents to their children through specific genetic mutations.



Is Hereditary Angioedema contagious?


Hereditary Angioedema (HAE) is a rare genetic disorder that affects the immune system and causes recurrent episodes of swelling in various parts of the body. It is important to note that HAE is not contagious and cannot be transmitted from one person to another.


HAE is an inherited condition, meaning it is passed down from parents to their children through specific genetic mutations. It is caused by a deficiency or dysfunction of a protein called C1 inhibitor, which plays a crucial role in regulating the immune response and preventing excessive swelling.


The symptoms of HAE typically include sudden and severe swelling in the hands, feet, face, gastrointestinal tract, or airways. These episodes can be unpredictable and may last for several days. The swelling can be painful, disfiguring, and potentially life-threatening, especially if it affects the airways and leads to difficulty breathing.


While HAE is not contagious, it is important to understand that it is a chronic condition that requires ongoing management and treatment. Individuals with HAE may experience frequent episodes of swelling, which can significantly impact their quality of life. It is crucial for them to work closely with healthcare professionals to develop a personalized treatment plan.


Diagnosis and Treatment


Diagnosing HAE can be challenging because its symptoms can resemble those of other conditions. However, a thorough medical evaluation, including a detailed family history, blood tests, and specialized laboratory tests, can help confirm the diagnosis.


Once diagnosed, treatment options for HAE aim to prevent or manage swelling episodes and minimize their impact. This may involve the use of medications such as C1 inhibitor replacement therapy, which helps restore the deficient protein and reduce the frequency and severity of attacks. Other medications, such as bradykinin receptor antagonists, may also be prescribed to alleviate symptoms during an acute attack.


Additionally, individuals with HAE are often advised to identify and avoid triggers that may precipitate swelling episodes. Common triggers include stress, trauma, hormonal changes, certain medications, and infections. By understanding and managing these triggers, individuals with HAE can potentially reduce the frequency and severity of their symptoms.


Conclusion


In summary, Hereditary Angioedema is a genetic disorder that is not contagious. It is caused by a deficiency or dysfunction of the C1 inhibitor protein and leads to recurrent episodes of swelling. While HAE can significantly impact an individual's life, it can be managed with appropriate treatment and lifestyle modifications. If you suspect you or someone you know may have HAE, it is important to consult with a healthcare professional for an accurate diagnosis and personalized management plan.


Diseasemaps
4 answers
No , it cannot be spread through germs

Posted May 23, 2017 by Donna 2250
No.. it is either inherented from a parent or it can spontaneously mutate

Posted Nov 29, 2017 by [email protected] 2300
Hereditary Angioedema is not contagious. It’s a hereditary condition.

Posted Nov 29, 2017 by Cham 100

Is Hereditary Angioedema contagious?

Hereditary Angioedema life expectancy

What is the life expectancy of someone with Hereditary Angioedema?

9 answers
Celebrities with Hereditary Angioedema

Celebrities with Hereditary Angioedema

1 answer
Is Hereditary Angioedema hereditary?

Is Hereditary Angioedema hereditary?

6 answers
Natural treatment of Hereditary Angioedema

Is there any natural treatment for Hereditary Angioedema?

5 answers
ICD9 and ICD10 codes of Hereditary Angioedema

ICD10 code of Hereditary Angioedema and ICD9 code

4 answers
Living with Hereditary Angioedema

Living with Hereditary Angioedema. How to live with Hereditary Angioedema?

8 answers
Hereditary Angioedema diet

Hereditary Angioedema diet. Is there a diet which improves the quality of l...

8 answers
History of Hereditary Angioedema

What is the history of Hereditary Angioedema?

3 answers

World map of Hereditary Angioedema

Find people with Hereditary Angioedema through the map. Connect with them and share experiences. Join the Hereditary Angioedema community.

Stories of Hereditary Angioedema

HEREDITARY ANGIOEDEMA STORIES
Hereditary Angioedema stories
Mine started in 2009 with my first swell, it was my lips and cheek. That is the same time the ucartia started also. It took my Dr. 5 years to find something to help me control and survive my Angioedema. I never knew how bad this could be till I was d...
Hereditary Angioedema stories
Desde niño tuve que soportar los diversos episodios de AEH sin saberlo, pasando de medico en medico con diversidad de diagnosticos y ordenes de cirugias innecesarias, gracias a Dios no acudi a ninguna. Fue hace tres años que optuve el diagnostico r...
Hereditary Angioedema stories
My earliest memory of HAE symptoms was when I was about 6 or 7.  I would occasionally get the abdomen swelling, be sick and sweating all day, then I would finally vomit and then feel better, go to sleep and be better the next morning.  I consider m...
Hereditary Angioedema stories
I was diagnosed accidentally, after seeing a TV show where the host talked about her HAE in 2014. My first attack was at 8, when I was mistakenly hospitalized with appendicitis.  The surgery wasn't done, because I felt better in 3 days.  Next reme...
Hereditary Angioedema stories
i was dx in 2008 with my first fasel swell . im hae type 2 . im co founder of the facebook group ( https://www.facebook.com/groups/156649074393978/ )

Tell your story and help others

Tell my story

Hereditary Angioedema forum

HEREDITARY ANGIOEDEMA FORUM
Hereditary Angioedema forum
Hi All, Is anyone aware of Cinryze experiencing a shortage supply? If so, why and where is this shortage (US or Europe)?   Thanks!
Hereditary Angioedema forum
Hi All, Is anyone aware of Cinryze experiencing a shortage supply? If so, why and where is this shortage (US or Europe)?   Thanks!
Hereditary Angioedema forum
Hi All, For those of you currently (or in the past) taking Cinryze, Firazyr, or Kalbitor, has Shire always paid for your co-pays through the co-pay assistance program or was there a limit to how much they paid? I've also heard that the case managers...
Hereditary Angioedema forum
Hi Everyone, I am interested in understanding and learning about your perspective on treatments and services available for HAE. What happens when you lose insurance and you need to obtain treatment? During this time, are you given treatment fre...
Hereditary Angioedema forum
Hi Everyone, I'm trying to understand what it is like for people with HAE. Therefore, would you ever switch treatment? Why or why not? What happens if you lose insurance coverage? Are you still recieving treatment? Was there a time where you had to ...

Ask a question and get answers from other users.

Ask a question

Find your symptoms soulmates

From now on you can add your symptoms in diseasemaps and find your symptoms soulmates. Symptoms soulmates are people with similar symptoms to you.

Symptoms soulmates

Add your symptoms and discover your soulmates map

Soulmates map