Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome

Keyphrases

• Jaundice 100%
• β-Thalassemia (β-thal) 100%
• Crigler-Najjar Syndrome 100%
• UGT1A1 66%
• Novel mutation 33%
• Coinheritance 33%
• Gene Coding 33%
• Hyperbilirubinemia 33%
• Exon 3 33%
• Rare Disorders 33%
• Gilbert Syndrome 33%
• Bilirubin Metabolism 33%
• Base Substitution 33%

Medicine and Dentistry

• Jaundice 100%
• Crigler-Najjar Syndrome 100%
• Thalassemia Major 100%
• Base 33%
• Orphan Disorder 33%
• Gilbert's Syndrome 33%
• Hyperbilirubinemia 33%
• Bilirubin Metabolism 33%
• Exon 33%