Neonatal hemochromatosis

A hereditary autosomal recessive disorder characterized by LIVER FAILURE in the neonatal period and heavy iron staining in the liver. There are also iron deposits in extrahepatic tissues, including the heart and pancreas. OMIM: 231100

Also Known As:

Alloimmune Hepatitis, Congenital; Giant cell hepatitis; Hemochromatosis, Neonatal; Idiopathic Neonatal Hemochromatosis; Neonatal hepatitis; PIGCH post infantile giant cell hepatitis

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Metal Metabolism
      - Hemochromatosis: 4165
        Neonatal hemochromatosis: 387
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Metal Metabolism
      - Hemochromatosis: 4165
        Neonatal hemochromatosis: 387
  - Iron Metabolism Disorders: 78
    - Iron Overload: 7614
      - Hemochromatosis: 4165
        Neonatal hemochromatosis: 387

Maria V Escolano-Margarit Selected Research

Maria V Escolano-Margarit Research Topics

Disease

Therapy/Procedure