Progeria risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
The most potent risk factor in the development of [[Hutchinson-Gilford progeria syndrome]] is [[mutation]] in [[LMNA]] [[gene]]. | |||
The most potent risk factor in the development of Hutchinson-Gilford progeria syndrome is mutation in LMNA gene. | |||
==Risk Factors== | ==Risk Factors== | ||
* The most potent risk factor in the development of Hutchinson-Gilford progeria syndrome is mutation in LMNA gene. | * The most potent risk factor in the development of [[Hutchinson-Gilford progeria syndrome]] is [[mutation]] in [[LMNA]] [[gene]]. | ||
*Other than genetic | *Other than [[Genetics|genetic]] there are no other [[Risk factor|risk factors]] mentioned | ||
==References== | ==References== | ||
Revision as of 14:02, 21 July 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]
Overview
The most potent risk factor in the development of Hutchinson-Gilford progeria syndrome is mutation in LMNA gene.
Risk Factors
- The most potent risk factor in the development of Hutchinson-Gilford progeria syndrome is mutation in LMNA gene.
- Other than genetic there are no other risk factors mentioned