Hutchinson-Gilford syndrome

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Hutch·in·son-Gil·ford syndrome (h

n-s

n-g

rd)

See progeria.

[After Sir Jonathan Hutchinson (1828-1913) and Hastings Gilford (1861-1941), British physicians.]

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progeria

This PA is a new initiative to support research to understand how mutations in the gene for lamin A/C affect nuclear structure, thus leading to bothdysfunction of the nuclear envelope, and depending on the mutation, Hutchinson-Gilford syndrome in humans (Eriksson et al.

The Biological Basis of Hutchinson-Gilford Syndrome (HGS): ... by Environmental Health Perspectives

These range from Down Syndrome (1 in 660 live births) to Hutchinson-Gilford Syndrome (1 in 250,000 live births).

Another look at facial disfigurement by Elks, Martin A. / The Journal of Rehabilitation

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