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Overview: Alagille syndrome (AS) is an autosomal dominant disorder (OMIM 118450) associated with abnormalities of the liver, heart, skeleton, eye, and kidneys and a characteristic facial appearance.1 In 1973, Watson and Miller reported 9 cases of ... ... Presentation of Alagille syndrome (AS) varies.
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Alagille syndrome - Wikipedia, the free encyclopedia
Alagille syndrome is a genetic disorder that affects the liver, heart, and other systems of the body. Problems associated with the disorder generally become evident in infancy or early childhood. The...
en.wikipedia.org/wiki/Alagille_syndrome |
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Join the Alagille Syndrome Facebook Group: Click Here!; Join and/or donate to the Alagille Syndrome Alliance through our cause page: Click Here!; ... Do you belong to the Alagille Syndrome Alliance Facebook group? Please join the group now and donate to the Alliance through facebook. Just click on the links below.
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Describes Alagille syndrome, a rare, inherited disorder that affects the liver. Covers the causes, symptoms, diagnosis, treatment, and long-term outlook. ... What is Alagille syndrome?
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Alagille syndrome is a genetic disorder that can affect the liver, heart, and other systems of the body. ... Signs and symptoms arising from liver damage in Alagille syndrome may include a yellowish tinge in the skin and the whites of the eyes (jaundice), itching, and deposits of cholesterol in the skin (xanthomas).
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Symptoms, Treatment and Prevention of Alagille Syndrome ... Definition of Alagille Syndrome ... Causes and Risk Factors of Alagille Syndrome...
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The offspring of an individual with Alagille syndrome have a 50% chance of having Alagille syndrome. Prenatal testing is possible if the JAG1 disease-causing mutation or a deletion detected by FISH is identified in an affected family member.
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ClinicalTrials.gov: Alagille Syndrome (National Institutes of Health) ... Genetics Home Reference: Alagille syndrome (National Library of Medicine) ... Alagille Syndrome(American Liver Foundation)
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