Novel Heterozygous Mutations in JAG1 and NOTCH2 Genes in a Neonatal Patient with Alagille Syndrome
Alagille Syndrome (ALGS) is a rare autosomal dominant disorder that affects multiple organ systems. Cholestasis as a result of a paucity of intrahepatic bile ducts and congenital heart defects are the two most common features of ALGS. We describe a case of ALGS with novel mutations of JAG1 and NOTCH...
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Hindawi Limited,
2017-01-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |