Alagille syndrome: Review of 14 patients

Alagille syndrome (AGS) Is a common form of familial intrahepatic choleslasis, an autosomal dominant disorder due to defects in Jagged1 gene. It Is characterized by at least 3 of 5 mator features. We reviewed two groups of patients with AGS. Group 1 comprised 12 AGS patients, retrospectively studied...

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Autori principali: Purnamawati S. Pujiarto (Autore), Arnold L. Smith (Autore)
Natura: Libro
Pubblicazione: Indonesian Pediatric Society Publishing House, 2017-02-01T00:00:00Z.
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