Iron is an essential micronutrient and a critical component of oxygen transport, numerous metabolic enzymes, and reaction centers of redox enzymes. Elevated iron can lead to iron accumulation in parenchymal organs, which can result in cardiac symptoms, diabetes, and severe liver diseases. Moreover, it is associated with severe infections, neurodegenerative disorders, musculoskeletal disorders, and other forms of cancer. Iron overload is related to many genetic and inherited conditions, including hereditary hemochromatosis. It is imperative that healthcare providers are familiar with hereditary hemochromatosis as early detection and therapeutic phlebotomy can prevent complications of iron overload when initiated before organ damage occurs. T...
Recent years have witnessed tremendous advances in the fields of pathophysiology, diagnosis and mana...
Homozygosity for the C282Y mutation is one of the most common genetic disorders, which predisposes t...
Haemochromatosis is most commonly due to the autosomal recessive inheritance of a C282Y substitution...
ABSTRACT: Hereditary Hemochromatosis (HH) is an autosomal recessive genetic disease characterized by...
Due to its pivotal role in orchestrating vital cellular functions and metabolic processes, iron is a...
Due to its pivotal role in orchestrating vital cellular functions and metabolic processes, iron is a...
Hemochromatosis, or iron accumulation, is an inherited disorder characterized by an excessively high...
Hereditary hemochromatosis is the most common cause of iron overload in adults and is probably the s...
Hereditary hemochromatosis (HH) comprises a group of inherited disorders of iron metabolism that can...
Hereditary hemochromatosis (HH) comprises a group of inherited disorders of iron metabolism that can...
Hereditary hemochromatosis is a disorder that causes the body to absorb too much iron from the diet....
Hemochromatosis comprises a group of inherited disorders resulting from mutations of genes involved ...
Hereditary hemochromatosis is a common inherited disorder of the iron metabolism. Screening studies ...
HFE-related hereditary haemochromatosis (HH) is an iron overload disease attributed to the highly pr...
Hereditary hemochromatosis is a common inherited disorder of the iron metabolism. Screening studies ...
Recent years have witnessed tremendous advances in the fields of pathophysiology, diagnosis and mana...
Homozygosity for the C282Y mutation is one of the most common genetic disorders, which predisposes t...
Haemochromatosis is most commonly due to the autosomal recessive inheritance of a C282Y substitution...
ABSTRACT: Hereditary Hemochromatosis (HH) is an autosomal recessive genetic disease characterized by...
Due to its pivotal role in orchestrating vital cellular functions and metabolic processes, iron is a...
Due to its pivotal role in orchestrating vital cellular functions and metabolic processes, iron is a...
Hemochromatosis, or iron accumulation, is an inherited disorder characterized by an excessively high...
Hereditary hemochromatosis is the most common cause of iron overload in adults and is probably the s...
Hereditary hemochromatosis (HH) comprises a group of inherited disorders of iron metabolism that can...
Hereditary hemochromatosis (HH) comprises a group of inherited disorders of iron metabolism that can...
Hereditary hemochromatosis is a disorder that causes the body to absorb too much iron from the diet....
Hemochromatosis comprises a group of inherited disorders resulting from mutations of genes involved ...
Hereditary hemochromatosis is a common inherited disorder of the iron metabolism. Screening studies ...
HFE-related hereditary haemochromatosis (HH) is an iron overload disease attributed to the highly pr...
Hereditary hemochromatosis is a common inherited disorder of the iron metabolism. Screening studies ...
Recent years have witnessed tremendous advances in the fields of pathophysiology, diagnosis and mana...
Homozygosity for the C282Y mutation is one of the most common genetic disorders, which predisposes t...
Haemochromatosis is most commonly due to the autosomal recessive inheritance of a C282Y substitution...