15

Is Congenital Sucrase Isomaltase Deficiency contagious?

Is Congenital Sucrase Isomaltase Deficiency transmitted from person to person? Is Congenital Sucrase Isomaltase Deficiency contagious? What are the routes of contagion? People with experience in Congenital Sucrase Isomaltase Deficiency help solve this question.

Is Congenital Sucrase Isomaltase Deficiency contagious?

Congenital Sucrase Isomaltase Deficiency (CSID) is a rare genetic disorder that affects the ability to digest certain sugars. It is not contagious and cannot be transmitted from person to person. CSID is an inherited condition caused by mutations in the sucrase-isomaltase gene. Individuals with CSID lack or have reduced levels of the sucrase-isomaltase enzyme, leading to difficulty in breaking down sucrose and starch. This condition is not contagious and is present from birth.



Congenital Sucrase Isomaltase Deficiency (CSID) is a rare genetic disorder that affects the digestive system. It is characterized by the body's inability to properly break down and absorb certain sugars, such as sucrose and maltose. This deficiency is caused by mutations in the sucrase-isomaltase gene.



CSID is not contagious. It is an inherited condition, meaning it is passed down from parents to their children through genetic factors. The disorder is present from birth and affects individuals throughout their lifetime. It is important to note that CSID is not caused by any external factors or infectious agents.



Individuals with CSID may experience a range of symptoms, including diarrhea, abdominal pain, bloating, and gas, after consuming foods or drinks containing sucrose or maltose. These symptoms can vary in severity and may require dietary modifications and enzyme replacement therapy to manage.



While CSID itself is not contagious, it is important for individuals with the condition to be aware of their dietary restrictions and to communicate them to others. This can help prevent misunderstandings and ensure that appropriate accommodations are made when it comes to shared meals or food preparation.


Diseasemaps
3 answers
No, nope, nada, not in the slightest.

Posted Mar 8, 2019 by Simone 3215
It is not contagious

Posted Nov 15, 2021 by Tracey 3000

Is Congenital Sucrase Isomaltase Deficiency contagious?

Congenital Sucrase Isomaltase Deficiency life expectancy

What is the life expectancy of someone with Congenital Sucrase Isomaltase D...

4 answers
Celebrities with Congenital Sucrase Isomaltase Deficiency

Celebrities with Congenital Sucrase Isomaltase Deficiency

2 answers
Is Congenital Sucrase Isomaltase Deficiency hereditary?

Is Congenital Sucrase Isomaltase Deficiency hereditary?

4 answers
Natural treatment of Congenital Sucrase Isomaltase Deficiency

Is there any natural treatment for Congenital Sucrase Isomaltase Deficiency...

3 answers
ICD9 and ICD10 codes of Congenital Sucrase Isomaltase Deficiency

ICD10 code of Congenital Sucrase Isomaltase Deficiency and ICD9 code

3 answers
Living with Congenital Sucrase Isomaltase Deficiency

Living with Congenital Sucrase Isomaltase Deficiency. How to live with Cong...

3 answers
Congenital Sucrase Isomaltase Deficiency diet

Congenital Sucrase Isomaltase Deficiency diet. Is there a diet which improv...

3 answers
History of Congenital Sucrase Isomaltase Deficiency

What is the history of Congenital Sucrase Isomaltase Deficiency?

2 answers

World map of Congenital Sucrase Isomaltase Deficiency

Find people with Congenital Sucrase Isomaltase Deficiency through the map. Connect with them and share experiences. Join the Congenital Sucrase Isomaltase Deficiency community.

Stories of Congenital Sucrase Isomaltase Deficiency

CONGENITAL SUCRASE ISOMALTASE DEFICIENCY STORIES
Congenital Sucrase Isomaltase Deficiency stories
Diagnosed at age 6 in Melbourne. No known family history of disease. No sucraid available in Australia so diet only to treat condition. Normal lactase enzyme but sucrase and maltase levels extremely low or non existent.  
Congenital Sucrase Isomaltase Deficiency stories
My son has CSID. Diagnosed at 5 years of age. It's been a long journey to get to this point.  As there is no access to sucraid in Australia, we are purely trying to manage by diet alone.  As a mother, I will always be a voice for my young son and...
Congenital Sucrase Isomaltase Deficiency stories
my name is Millie and I was diagnosed with SI at age 18 months as I didn't fall under the top four genetic mutations of CSID and it was too expensive to continue testing, but I follow the exact same diet and can't have sucrose or much starch. I have ...

Tell your story and help others

Tell my story

Congenital Sucrase Isomaltase Deficiency forum

CONGENITAL SUCRASE ISOMALTASE DEFICIENCY FORUM
Congenital Sucrase Isomaltase Deficiency forum
Hello, Just curious, do any of you struggle with UHT milk? I am fine with all other dairy but for some reason UHT is a no go for me. For the life of me I can't figure out why, there are no added sugars. I'm wondering if this is a 'CSID thin...

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