Review
Copyright ©The Author(s) 2024.
World J Gastroenterol. Mar 7, 2024; 30(9): 1043-1072
Published online Mar 7, 2024. doi: 10.3748/wjg.v30.i9.1043
Table 3 Disorders associated with nonsyndromic bile duct paucity in children[109,110]
Disease type
Cause
Metabolic and genetic disordersAlpha-1 antitrypsin deficiency
Cystic fibrosis
Peroxisomal disorders
Niemann pick type C
Kabuki syndrome (rare)
Chromosomal abnormality (trisomy 17, 18, or 21) (rare)
InfectionsCongenital cytomegalovirus, syphilis, and rubella infection
Inflammatory and immune disordersHemophagocytic lymphohistiocytosis
Graft-versus-host disease
Chronic hepatic allograft rejection
Sclerosing cholangitis (primary or secondary)
Biliary atresia (late)
OthersDrug- or antibiotic-associated vanishing bile duct syndrome
Panhypopituitarism
Idiopathic