Biliary atresia differential diagnosis: Difference between revisions
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*[[Caroli's disease|Caroli]] Disease | *[[Caroli's disease|Caroli]] Disease | ||
*Cystic Fibrosis | *Cystic Fibrosis | ||
*Toxoplasmosis, other infections, rubella, cytomegalovirus infection, and herpes simplex [TORCH] | *Toxoplasmosis, other infections, rubella, cytomegalovirus infection, and herpes simplex [TORCH]<ref name="pmid15817506">{{cite journal| author=Mack CL, Sokol RJ| title=Unraveling the pathogenesis and etiology of biliary atresia. | journal=Pediatr Res | year= 2005 | volume= 57 | issue= 5 Pt 2 | pages= 87R-94R | pmid=15817506 | doi=10.1203/01.PDR.0000159569.57354.47 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15817506 }} </ref> | ||
==References== | ==References== |
Revision as of 10:35, 17 February 2022
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Causes of neonatal cholestasis that should be distinguished from biliary atresia include
- Byler disease
- Congenital biliary dilatation
- Choledochal Cysts
- Cholestasis
- Galactose-1-Phosphate Uridyltransferase Deficiency (Galactosemia)
- Idiopathic neonatal hepatitis
- Inborn errors of bile acid synthesis
- Neonatal Hemochromatosis
- Intrahepatic bile duct hypoplasia
- Lipid Storage Disorders
- Caroli Disease
- Cystic Fibrosis
- Toxoplasmosis, other infections, rubella, cytomegalovirus infection, and herpes simplex [TORCH][1]
References
- ↑ Mack CL, Sokol RJ (2005). "Unraveling the pathogenesis and etiology of biliary atresia". Pediatr Res. 57 (5 Pt 2): 87R–94R. doi:10.1203/01.PDR.0000159569.57354.47. PMID 15817506.