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Bookmark or Share- Alagille Syndrome - Johns Hopkins MedicineAlagille syndrome is a genetic disorder in which you have fewer bile ducts than normal in your liver. Alagille syndrome can be passed from parent to child or happen naturally. Alagille syndrome not only affects the liver, it can also cause skin, heart, facial, kidney, and eye abnormalities.
- Alagille Syndrome - Children's Hospital of PhiladelphiaAlagille syndrome — also known as Alagille-Watson syndrome, syndromic bile duct paucity and arteriohepatic dysplasia — is an inherited liver disorder that also affects the heart, eyes, bones, kidneys, vasculature and other organs.
- Alagille Syndrome - GeneReviews® - NCBI BookshelfAlagille syndrome (ALGS) is a multisystem disorder with a wide spectrum of clinical variability ranging from life-threatening liver or cardiac disease to only subclinical manifestations (e.g., butterfly vertebrae, posterior embryotoxon, characteristic facial features) [Mitchell et al 2018, Kohut et al 2021].
- Alagille Syndrome: Symptoms, Causes & Treatment - Cleveland ClinicAlagille syndrome, also called Alagille-Watson syndrome, is a genetic condition that affects your liver and heart, along with other parts of your body. The condition can cause liver damage and structural heart abnormalities.
- Alagille syndrome | About the Disease | GARD - Genetic and Rare ...Alagille syndrome is a genetic syndrome that can affect the liver and other parts of the body. The liver problems result from having fewer small bile ducts than normal in the liver. This leads to bile building-up inside the liver, which in turn causes liver scarring and damage.
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