Biliary atresia differential diagnosis: Difference between revisions
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Causes of neonatal cholestasis that should be distinguished from biliary atresia include | |||
congenital biliary dilatation | |||
idiopathic neonatal hepatitis | |||
* [[Alagille syndrome|Alagille Syndrome]] | |||
* Byler disease | |||
* [[Choledochal cysts|Choledochal Cysts]] | |||
* Cholestasis | |||
* Galactose-1-Phosphate Uridyltransferase Deficiency (Galactosemia) | |||
* Idiopathic neonatal hepatitis | |||
* Inborn errors of bile acid synthesis | |||
* Lipid Storage Disorders | |||
* Neonatal Hemochromatosis | |||
* Nonsyndromic intrahepatic bile duct hypoplasia | |||
* Pediatric Caroli Disease | |||
* Pediatric Cytomegalovirus Infection | |||
* Pediatric Herpes Simplex Virus Infection | |||
* Pediatric Rubella | |||
* Sinonasal Manifestations of Cystic Fibrosis | |||
* Syphilis | |||
* Total parenteral nutrition–associated (TPN) cholestasis | |||
* Toxoplasmosis | |||
* Viral infections (eg, toxoplasmosis, other infections, rubella, cytomegalovirus infection, and herpes simplex [TORCH]) | |||
==References== | ==References== |
Revision as of 10:28, 17 February 2022
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Causes of neonatal cholestasis that should be distinguished from biliary atresia include
congenital biliary dilatation
idiopathic neonatal hepatitis
- Alagille Syndrome
- Byler disease
- Choledochal Cysts
- Cholestasis
- Galactose-1-Phosphate Uridyltransferase Deficiency (Galactosemia)
- Idiopathic neonatal hepatitis
- Inborn errors of bile acid synthesis
- Lipid Storage Disorders
- Neonatal Hemochromatosis
- Nonsyndromic intrahepatic bile duct hypoplasia
- Pediatric Caroli Disease
- Pediatric Cytomegalovirus Infection
- Pediatric Herpes Simplex Virus Infection
- Pediatric Rubella
- Sinonasal Manifestations of Cystic Fibrosis
- Syphilis
- Total parenteral nutrition–associated (TPN) cholestasis
- Toxoplasmosis
- Viral infections (eg, toxoplasmosis, other infections, rubella, cytomegalovirus infection, and herpes simplex [TORCH])