Alagille syndromeis a rarelivercondition that is passed down through families.

This inability is triggered by a lack of enoughbile ductsto drain bile properly.

This article discusses the symptoms, causes, and treatment options for people with Alagille syndrome.

Jaundice mono enlarged liver hepatomegaly

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This pathway triggers certain actions within the body that are important for fetal development.

When they mutate, that pathway is compromised.This causes developmental issues.

The mutated gene needs to come from just one of the two biological parents.

This is accomplished through a liverbiopsy, which involves removing a sample of tissue for examination in a lab.

Other tests may be used to examine different parts of the body associated with characteristics of the disease.

Medications designed to treat certain symptoms may also be used.

Other treatment options involve:

Can Alagille Syndrome Be Fatal?

That said, many people with the disease have a typical life expectancy the same as anyone else.

Prognosis

The prognosis of Alagille syndrome depends greatly on the severity of the disease.

Coping

Coping with Alagille syndrome depends on how it affects you.

Each person with the condition will present differently, and many cases are mild.

However, this rare disease can cause serious and even life-threatening complications, so treatment is always necessary.

Frequently Asked Questions

Most people with the disease have a low life expectancy.

There is no cure for Alagille syndrome.

Alagille syndrome is a genetic condition, so people are born with it.

Symptoms usually develop anytime within the first three months of life.

Johns Hopkins Medicine.Alagille syndrome.

Turnpenny PD, Ellard S.Alagille syndrome: pathogenesis, diagnosis and management.Eur J Hum Genet.

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