Alagille Syndrome

(Medicine) genetic condition characterized by facial and skeletal abnormalities and stricture of the pulmonary artery and bile ducts (often causes jaundice in newborn infants)

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 disorder is inherited in an autosomal dominant pattern, and the estimated prevalence of Alagille syndrome is 1 in every 70,000 live births.
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Syndrome /syn·drome/ a set of symptoms occurring together; the sum of signs of any morbid state; a symptom complex. See also entries under disease. [more]Alagille syndrome - Community and Resources