Biliary atresia differential diagnosis: Difference between revisions
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Causes of neonatal cholestasis that should be distinguished from biliary atresia include | Causes of neonatal cholestasis that should be distinguished from biliary atresia include | ||
* [[Alagille syndrome|Alagille Syndrome]] | |||
*Byler disease | |||
*Congenital biliary dilatation | |||
*[[Choledochal cysts|Choledochal Cysts]] | |||
*Cholestasis | |||
* | *Galactose-1-Phosphate Uridyltransferase Deficiency (Galactosemia) | ||
* | *Idiopathic neonatal hepatitis | ||
* [[Choledochal cysts|Choledochal Cysts]] | *Inborn errors of bile acid synthesis | ||
* Cholestasis | *Neonatal Hemochromatosis | ||
* Galactose-1-Phosphate Uridyltransferase Deficiency (Galactosemia) | *Intrahepatic bile duct hypoplasia | ||
* Idiopathic neonatal hepatitis | *Lipid Storage Disorders | ||
* Inborn errors of bile acid synthesis | *[[Caroli's disease|Caroli]] Disease | ||
*Cystic Fibrosis | |||
* Neonatal Hemochromatosis | *Toxoplasmosis, other infections, rubella, cytomegalovirus infection, and herpes simplex [TORCH] | ||
* | |||
* | |||
* | |||
* Toxoplasmosis | |||
==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]