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Alagille-Syndrom
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Beschreibung:
A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (), and malformations in the cardiovascular system, the eyes, the vertebral column, and the facies. Major clinical features include , and congenital heart disease with peripheral . Alagille syndrome may result from heterogeneous gene mutations, including mutations in JAG1 on (Type 1) and NOTCH2 on (Type 2).
Synonym(s):
Arteriohepatische Dysplasie /
Dysplasie, arteriohepatische /
Alagille-Syndrom 2 /
Alagille-Syndrom 1 /
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(NLM)®
(DIMDI - Deutsche Fassung)
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