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Hutchinson-Gilford Progeria: Difference between revisions
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[https://www.ncbi.nlm.nih.gov/pubmed/27374873 Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations] | [https://www.ncbi.nlm.nih.gov/pubmed/27374873 Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations] | ||
:[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5195863/ PMC5195863] | |||
{{Wikidata|Q213098}} | {{Wikidata|Q213098}} | ||
<references/> | <references/> | ||
Revision as of 13:23, 24 January 2019
Hutchinson-Gilford Disease (or syndrome) Progeria - early senescence in children with large skull, bird-like features, atrophy of skin, los subcutaneous fat, high serum lipid levels and early atherosclerotic changes in the vessels Progeria was first described in 1886 by two English surgeons Jonathan Hutchinson (Sir) and H. Gilford [1]
Hutchinson-Gilford progeria syndrome
Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations
- ↑ Dictionary of Medical eponyms Firkin BG and JA Whitworth Roche