Progeria: Difference between revisions
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Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS) is a very rare [[Genetic disorders|genetic disorder]]. It is characterised by rapid ageing and becmes apparent within the first two of years of life. | Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS) is a very rare [[Genetic disorders|genetic disorder]]. It is characterised by rapid ageing and becmes apparent within the first two of years of life. The average life expectancy for children with progeria is 13. The condition is caused by a [[Mutation|mutation]] in the [[LMNA gene|LMNA gene]], this [[gene|gene]] encodes proteins required for the maintenance of the cell structure. <br> | ||
There are distinct physical characteristics associated with progeria: | There are distinct physical characteristics associated with progeria: | ||
Latest revision as of 17:52, 4 December 2017
Progeria, also known as Hutchinson-Gilford Progeria Syndrome (HGPS) is a very rare genetic disorder. It is characterised by rapid ageing and becmes apparent within the first two of years of life. The average life expectancy for children with progeria is 13. The condition is caused by a mutation in the LMNA gene, this gene encodes proteins required for the maintenance of the cell structure.
There are distinct physical characteristics associated with progeria:
- alopecia (hair loss)
- joint stiffness
- lack of adipose tissue
- increased risk of heart disease, angina, stroke
- stunted growth