06 October 2022
: Case report
Pathogenic Novel Heterozygous Variant c.1076c>T p. (Ser359Phe) chr1: 120512166 in NOTCH2 Gene, Type 2 Alagille Syndrome Causing Neonatal Cholestasis: A Case Report
Unusual clinical course, Challenging differential diagnosis, Rare disease, Congenital defects / diseases
Mohammed Shahab Uddin


DOI: 10.12659/AJCR.935840
Am J Case Rep 2022; 23:e935840
Figure 2. Serum bilirubin curves from the first week of life till week 14. The red line represents the total serum bilirubin, and the blue line indicates direct serum bilirubin.