Table 1 Clinical diagnoses of the cohort of patients and PTCC findings (normal/abnormal)
Final Diagnosis | Number of Patients (%) | Normal PTCC | Abnormal PTCC |
|---|---|---|---|
Biliary Atresia | 26 (36%) | 0 | 26 |
TPN Cholestasis | 15 (21%) | 15 | 0 |
Neonatal Hepatitis | 12 (16%) | 12 | 0 |
Alagille Syndrome | 4 (5%) | 0 | 4 |
Progressive Familial Intrahepatic Cholestasis (PFIC) | 4 (5%) | 3 | 1 |
Williams Syndrome | 1 (1%) | 1 | 0 |
North American Indian Childhood Cirrhosis (NAICC) | 1 (1%) | 1 | 0 |
Alpha-1 Antitrypsin Deficiency | 1 (1%) | 0 | 1 |
G6PD Deficiency | 1 (1%) | 1 | 0 |
Hepatitis of Unknown Origin | 8 (11%) | 7 | 1 |
Total | 73 | 40 | 33 |