Wikisage, the free encyclopedia of the second generation, is digital heritage

Hutchinson-Gilford Progeria: Difference between revisions

From Wikisage
Jump to navigation Jump to search
m (File:Nihms-803560-f0004.jpg)
mNo edit summary
 
Line 1: Line 1:
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
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 [[Hastings Gilford|H. Gilford]] <ref>Dictionary of Medical eponyms Firkin BG and JA Whitworth Roche </ref>
Progeria was first described in 1886 by two English surgeons Jonathan Hutchinson (Sir) and [[Hastings Gilford|H. Gilford]] <ref>Dictionary of Medical eponyms Firkin BG and JA Whitworth Roche </ref>



Latest revision as of 13:30, 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

PMC5195863

miniature

Q213098 at Wikidata  Interwiki via Wikidata


  1. Dictionary of Medical eponyms Firkin BG and JA Whitworth Roche