Crigler-Najjar Syndrome

A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.

Also Known As:

Crigler Najjar Syndrome; Crigler Najjar Syndrome, Type 1; Crigler-Najar Syndrome; Crigler-Najjar Syndrome, Type I; Familial Nonhemolytic Unconjugated Hyperbilirubinemia; Hereditary Unconjugated Hyperbilirubinemia; Crigler Najar Syndrome; Crigler Najjar Syndrome, Type I; Crigler Najjar Syndromes; Hereditary Unconjugated Hyperbilirubinemias; Hyperbilirubinemia, Hereditary Unconjugated; Najjar Syndrome, Crigler; Syndrome, Crigler Najjar; Unconjugated Hyperbilirubinemia, Hereditary

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inborn Errors Metabolism: 1183
    - Hereditary Hyperbilirubinemia: 38
      - Crigler-Najjar Syndrome: 247
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10634
  - Inborn Errors Metabolism: 1183
    - Hereditary Hyperbilirubinemia: 38
      - Crigler-Najjar Syndrome: 247

Francisco Cañabate Reche Selected Research

Francisco Cañabate Reche Research Topics

Disease

Drug/Important Bio-Agent (IBA)