Hutchinson-Gilford Progeria Syndrome: A Premature Aging Disease.

doi:10.1007/s12035-017-0610-7

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Article

Hutchinson-Gilford Progeria Syndrome: A Premature Aging Disease.

Molecular neurobiology - 1 May 2018

Ahmed Muhammad Saad, Ikram Sana, Bibi Nousheen, Mir Asif

Abstract excerpt

Progeria is sporadic, very rare, autosomal dominant, deadly childhood disorder. It is one of the progeroid syndromes also known as Hutchinson-Gilford progeria syndrome (HGPS). Aging is a developmental process that begins with fertilization and ends up with death involving a lot of environmental and genetic factors. The disease firstly involves premature aging and then death from complications of atherosclerosis...

Topics

Aging, Premature
Genetic Predisposition to Disease
Humans
Inheritance Patterns
Prenatal Diagnosis
Progeria

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Open in PubMed

Identifiers

PMID: 28660486
DOI: 10.1007/s12035-017-0610-7

Genes

LMNA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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