Description, Causes and Risk Factors:
Alagille syndrome is an inherited disorder that mimics other forms of prolonged liver disease seen in infants and young children. However, a group of unusual features in other organ systems distinguishes Alagille syndrome from other liver and bile duct diseases in infants. Specifically, Alagille syndrome is also associated with cardiac disease, eye and skeletal findings and a characteristic facial appearance. The blood vessels and kidneys may also be involved in a smaller proportion of cases.
Children with Alagille syndrome usually have a liver disease characterized by a progressive loss of the bile ducts within the liver over the first year of life. This leads to a buildup of bile in the liver, causing damage to liver cells. Scarring may occur and lead to cirrhosis in about 30 to 50 per cent of affected children.
Alagille syndrome is caused by changes, or mutations, in one of two genes, usually JAGGED1 or occasionally NOTCH2. In approximately 60 per cent of the cases of Alagille syndrome, the gene change is the result of a new mutation that occurs in that baby. In other 40 per cent of cases, the gene mutation is inherited from one of the parents. A parent carrying a disease-causing mutation has a 50 percent chance of transmitting that gene to any subsequent children. Each affected adult or child may have all or only a few of the features of the syndrome. Even individuals in the same family, sharing the same gene mutation have variable manifestations in each of the affected organ systems.
The syndrome occurs in about one in every 70,000 births and is equally common in boys and girls. The symptoms of Alagille syndrome are usually seen in the first 2 years of life.
Not all individuals with Alagille syndrome have significant liver disease, though probably the majority does. Typically, symptoms of the illness are jaundice and poor growth within the first three months of life. Later, there is persistent jaundice, severe itching, fatty deposits in the skin (xanthomas) and poor growth during early childhood. Frequently the disease stabilizes between ages five and eight with an improvement in symptoms.
Other features which help establish the diagnosis include abnormalities in the cardiovascular system, the spinal bones, the eye and the kidneys. Heart involvement typically involves narrowing of the blood vessel connecting the heart to the lungs (pulmonary artery) which ranges in severity, but may also include a simple heart murmur or a severe congenital heart problem. The shape of the bones of the spinal column may often look like the wings of a butterfly on x-ray, but this does not cause any problems. There is also a specific facial appearance shared by children with Alagille syndrome that makes them easily recognizable. The features include a prominent, broad forehead, deep-set eyes, a straight nose and a small pointed chin.
The majority of children with Alagille syndrome have an abnormality of the eyes in which an extra, circular line on the surface of the eye can be detected by a specialized eye examination. However, it does not lead to any vision problems.
In addition, some children have various abnormalities in their kidneys. In approximately 15 per cent of individuals with Alagille syndrome there is a risk of bleeding in the head and brain (stroke).
Because the symptoms of Alagille syndrome vary and because the syndrome is sorare, the disorder can be difficult to diagnose. The doctor will perform a thoroughphysical examination to look for clinicalsymptoms of the disorder. If Alagille syndrome is suspected, the doctor will orderone or more of the following tests andexaminations:
An abdominal ultrasound to look for liver enlargement and to rule out otherconditions.
A liver biopsy to check for decreased number of hepatic ducts.
A cardiology examination to check for heart problems.
An eye examination to check for posterior embryotoxon.
An x-ray of the spine to look for abnormalities.
Examinations of the blood vessels and kidneys to check for abnormalities.
Blood tests to check liver function and nutritional status.
To make a diagnosis of Alagille syndrome,a positive liver biopsy and the presence ofthree of the following symptoms are usuallyrequired:
Heart abnormalities or murmurs.
The doctor may also have a blood sampletested to look for the JAG1 gene mutation. The gene mutation can be identifiedin 95 percent of people with a diagnosis ofAlagille syndrome based on signs and symptoms.A person can also be diagnosed withAlagille syndrome if the JAG1 gene mutation alone is present—even when no majorsymptoms of the disorder are evident.
Treatment of Alagille syndrome is primarily medical and not surgical and is based on trying to increase the flow of bile from the liver, maintain normal growth and development, and prevent or correct any of the specific nutritional deficiencies that often develop. Because bile flow from the liver to the intestine is slow in Alagille syndrome, medications designed to increase the flow of bile are frequently prescribed. This may decrease the damage in the liver and improve the digestion of fat and fat soluble vitamins.
Itching caused by the buildup of bile in the blood and skin may be relieved by medications (e.g. ursodeoxycholic acid, cholestyramine). Elevations in blood cholesterol also respond to the medications used to increase bile flow. Elevated blood cholesterol levels can lead to small yellow deposits of cholesterol on the skin of knees, elbows, palms, eyelids and other surfaces that are frequently rubbed (xanthomas).
Although reduced flow of bile into the intestine leads to poor digestion of dietary fat, a specific type of fat can still be well digested and therefore infant formulas containing high levels of medium-chain triglycerides (MCT) are usually substituted for conventional formulas in infants. Some infants can grow adequately on breast milk if additional MCT oil is given. Foods containing high fat levels may lead to looser, greasy stools later in childhood. However, the benefits from the calories and vitamins in the fat that is absorbed usually leads to the recommendation that the child not be put on a low-fat diet. There are no other dietary restrictions. Occasionally, MCT oil is also prescribed as a nutritional supplement in infancy.
Problems with fat digestion and absorption may lead to a deficiency of fat-soluble vitamins (A, D, E and K). Vitamin A deficiency causes night blindness and red eyes. Vitamin D deficiency causes softening and fractures of the bones and teeth. Vitamin E deficiency causes a disabling disease of the nervous system and muscles, and vitamin K deficiency causes bleeding problems and has been associated with poor bone health as well. Deficiencies of these vitamins can be diagnosed by blood tests and usually can be corrected by vitamin supplements.
There is presently no procedure that can correct the loss of the bile ducts within the liver. In 20 to 30 per cent of patients, liver cirrhosis advances to a stage where the liver fails to perform its functions. Liver transplantation is then considered.
The overall life expectancy for children with Alagille syndrome is unknown, but depends on several factors: the severity of scarring in the liver and/or the need for liver transplantation, the risk of stroke and whether heart or lung problems develop because of the narrowing in the pulmonary artery. Many adults with Alagille syndrome are leading normal lives.
NOTE: The above information is for processing purpose. The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition.
DISCLAIMER: This information should not substitute for seeking responsible, professional medical care.
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