Alagille syndrome and Wilson disease in siblings: A diagnostic conundrum

Keyphrases

• 18 Years Old 20%
• 24-hour Urine Collection 20%
• Abnormal Liver Function 20%
• Alagille Syndrome 100%
• ATP7B 20%
• Ceruloplasmin 20%
• Cholestasis 20%
• Copper Concentration 20%
• Disease Genes 20%
• Disease Screening 20%
• Family Members 20%
• Heterozygote 20%
• Liver 20%
• Liver Function 20%
• Liver Function Tests 20%
• Rare Genetic Disease 20%
• Recently Diagnosed 20%
• Somatic mutation Analysis 20%
• Synthetic Function 20%
• Urine Copper 20%
• Ursodiol 20%
• Wilson Disease 100%
• Young Men 20%

Medicine and Dentistry

• Alagille Syndrome 100%
• Ceruloplasmin 20%
• Cholestasis 20%
• Clinician 20%
• Diagnosis 100%
• Disease 20%
• Gene Mutation 20%
• Heterozygote 20%
• Index Case 20%
• Liver Function 40%
• Liver Function Test 20%
• Ursodeoxycholic Acid 20%
• Wilson's Disease 100%