Iron overload in an HFE heterozygous carrier: A case report and literature review

Keyphrases

• Iron Overload 100%
• Heterozygous Carrier 100%
• C282Y 100%
• Hemochromatosis 66%
• Hereditary Hemochromatosis 66%
• H63D 66%
• S65C 66%
• Iron Absorption 66%
• Clinical Manifestations 33%
• Dysregulation 33%
• Phlebotomy 33%
• Gain-of-function mutation 33%
• Codon 33%
• Alanine Aminotransferase 33%
• Caucasian Women 33%
• Autosomal Recessive 33%
• Aminotransferase Levels 33%
• Aspartate Aminotransferase 33%
• Liver Function Tests 33%
• Serum Ferritin 33%
• Phenotypic Expression 33%
• Membrane Expression 33%
• HFE Gene 33%
• Hemochromatosis Gene 33%
• Iron Metabolism 33%
• Tissue Deposition 33%
• Transferrin Saturation 33%
• T-accounts 33%

Biochemistry, Genetics and Molecular Biology

• Iron Poisoning 100%
• Iron Overload 100%
• Genetic Carrier 100%
• Heterozygote 100%
• Iron Absorption 100%
• Codon 50%
• Autosomal Recessive Disorder 50%
• Ferritin Blood Level 50%
• Loss of Function Mutation 50%
• Alanine Transaminase 50%
• Phlebotomy 50%
• Liver Function Test 50%
• Iron Metabolism 50%
• Transferrin Saturation 50%
• Aspartate Aminotransferase Level 50%
• HFE (Gene) 50%

Medicine and Dentistry

• Iron Overload 100%
• Hemochromatosis 100%
• Heterozygote 100%
• Iron Absorption 40%
• Ferritin 20%
• Alanine Aminotransferase 20%
• Aspartate Aminotransferase 20%
• Liver Function Test 20%
• Autosomal Recessive Disorder 20%
• Codon 20%
• Phlebotomy 20%
• Loss of Function Mutation 20%
• Transferrin Saturation 20%
• Iron Metabolism 20%