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Alagille Syndrome: Causes, Symptoms, Diagnosis, and Treatment

April 18, 2025

Alagille Syndrome: Causes, Symptoms, Diagnosis, and Treatment
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Alagille Syndrome is a congenital syndrome that usually affects the heart and the liver. Signs of it first show up in infancy or childhood. It is a rare condition, affecting one person in every 100,000. It destroys the bile duct progressively when it culminates in liver disease.

It also affects other organs of the body, such as the spine, kidneys, heart, and eyes. Generally, children who have this syndrome have the same facial characteristics: wide-set eyes, a sharp chin, and broad brows. This condition is seen equally among boys and girls of all ethnicities.

Causes

Alagille Syndrome is a congenital disease that is inherited from one’s parents. If one parent has the gene mutation for this disease, the child has a 50 per cent chance of being born with it. They may not develop the syndrome’s symptoms, yet the child is said to suffer from this condition and has a 50 per cent chance of passing it on to their next generation.

Symptoms

Its symptoms vary from child to child and are more or less severe than others. The first sign of this condition is jaundice and poor growth of the child during the first few months after detection. For children over three months of age, the symptoms of Alagille Syndrome are:

  • Severe body itch
  • Continuous jaundice
  • Fat deposits in the skin
  • Dark urine
  • White or grey stools
  • Poor weight gain
  • Poor body development
  • Heart murmur
  • Butterfly-shaped bones in the spine
  • Characteristic features: sharp chin, broad brow, and wide-set eyes

As a child with this syndrome grows, he will exhibit the following complications:

  • Diarrhoea
  • Problems relating to blood vessels and the heart
  • Delayed puberty
  • Liver failure
  • Kidney disease
  • Portal hypertension
  • kidney disease

Diagnosis

Though difficult to diagnose because its symptoms resemble other types of liver disease, Alagille’s Syndrome can be identified due to several other features. The doctor will usually ask for blood tests, an ultrasound, and a liver biopsy to be done. To know how much bile flows from the liver, a nuclear scan should be performed. In order to check the bile ducts and liver, surgery could also be performed.

Treatment

Alagille’s Syndrome has no cure, but surgery is not an answer to manage its symptoms. The doctor’s main goal is to ensure that there are no complications of the disease. Since there is less bile flow in this condition, patients of Alagille’s Syndrome could easily develop fat-soluble vitamin deficiency. The solution to this is to have fat-soluble Vitamins A, D, E, and K, which help digest fat faster.

Medication is given to reduce the body itch, and surgery is the answer if the heart needs to be surgically corrected. Liver transplantation is resorted to when the liver disease becomes chronic and cirrhosis sets in. 

Why Rela Hospital

When a baby is diagnosed with a rare condition, it’s a matter of grave concern for the whole family. Few people know of Alagille Syndrome, which only makes it worse. But with the patient counselling team at Dr Rela Hospital, Chennai, all your problems are eased with our counsellor explaining the nuances of this syndrome to you. This makes acceptance of the child’s problem easier for the parents to bear, while our expert surgeons play their role with confidence.

Parents of patients with these rare liver conditions need not worry because when they place their child in our care, we realize that it’s a huge responsibility and carry it out to perfection. Put this down to our team of expert liver surgeons who come to you with years of practice in foreign environments.

Plus, our hospital was founded by a world-renowned liver specialist, Dr. Rela, under whose guidance the hospital functions. With so much going for your baby, the infant can only go home well again soon.

We have a reputation for being the best in Alagille Syndrome treatment in India because of our team of experts who keep abreast of techniques in this field. Add to that, our hospital is completely outfitted with the latest technology, equipment, and trained nursing and support staff. These reasons make us the right choice for Paediatric liver transplantation in India, among other liver conditions.

Frequently Asked Questions

1. What is the life expectancy of an individual diagnosed with Alagille syndrome?

Individuals with mild Alagille syndrome often live a normal lifespan. However, those with more severe complications may have a shortened life expectancy. It’s important to discuss your specific symptoms with your healthcare provider, who will monitor your organ function through regular screening tests. The goal of treatment is to control symptoms and prevent serious health complications.

2. Can Alagille syndrome be prevented?

Alagille syndrome cannot be prevented because it is caused by genetic mutations. However, if you have a family history of the condition or are planning to have a child, consult your healthcare provider about genetic testing to better understand your risk of passing it on.

Disclaimer: We recommend consulting a Doctor before taking any action based on the above shared information.


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Department

HPB Surgery & Liver Transplantation

HPB Surgery & Liver Transplantation

Liver Disease & Transplantation

Liver Disease & Transplantation