Hutchinson-Gilford Progeria Syndrome: Clinical and Molecular Characterization.

HGPS genetic assessment laminopathy premature aging progeria treatment

Journal

The application of clinical genetics
ISSN: 1178-704X
Titre abrégé: Appl Clin Genet
Pays: New Zealand
ID NLM: 101579789

Informations de publication

Date de publication:
2020
Historique:
received: 15 11 2019
accepted: 13 05 2020
entrez: 18 9 2020
pubmed: 19 9 2020
medline: 19 9 2020
Statut: epublish

Résumé

Hutchinson-Gilford progeria syndrome (HGPS) is a rare congenital disease caused by mutations in the

Identifiants

pubmed: 32943904
doi: 10.2147/TACG.S238715
pii: 238715
pmc: PMC7481268
doi:

Types de publication

Case Reports

Langues

eng

Pagination

159-164

Informations de copyright

© 2020 Pachajoa et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

Références

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Auteurs

Harry Pachajoa (H)

Faculty of Health Sciences, Congenital Anomalies and Rare Diseases Investigation Center (CIACER), Universidad Icesi, Cali, Colombia.
Genetic Department, Fundacion Valle del Lili, Cali, Colombia.

Angelica Claros-Hulbert (A)

Pediatric Palliative Care Department, Fundacion Valle del Lili, Cali, Colombia.
Clinical Investigation Center (CIC), Fundacion Valle del Lili, Cali, Colombia.

Ximena García-Quintero (X)

Pediatric Palliative Care Department, Fundacion Valle del Lili, Cali, Colombia.
Clinical Investigation Center (CIC), Fundacion Valle del Lili, Cali, Colombia.

Lina Perafan (L)

Faculty of Health Sciences, Congenital Anomalies and Rare Diseases Investigation Center (CIACER), Universidad Icesi, Cali, Colombia.

Andres Ramirez (A)

Faculty of Health Sciences, Praxis Jessen² + Kollegen, Berlin, Germany.

Andres F Zea-Vera (AF)

Faculty of Health Sciences, Universidad del Valle, Cali, Colombia.

Classifications MeSH