Haemochromatosis - Learn more
Birth defects and genetics collection
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Animation, Educational, Special Interest
Haemochromatosis is a hereditary condition that causes your body to absorb too much iron from your diet. Over time it accumulates in tissues and certain organs, including your heart, liver and pancreas. If undetected and untreated, this excess iron can damage tissues and organs.
Up Next in Birth defects and genetics collection
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Phenylketonuria - Learn more
Phenylketonuria (PKU) is a genetic condition that prevents the breakdown of phenylalanine, an amino acid that plays an important role in metabolism. A build-up of phenylalanine in the body can lead to an intellectual disability.
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Progeria - Learn more
Progeria is a rare genetic disorder that causes a child to age rapidly, giving them an average life expectancy of 13 years. Symptoms begin to appear in the first two years of life. It’s also known as Hutchinson-Gilford progeria syndrome, or HGPS.
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Spina bifida - Learn more
Spina bifida is a birth defect involving the spine, spinal cord and the protective covering of the spinal cord, called the meninges. It is part of a group of disorders called neural tube defects that can occur to a foetus during pregnancy.
