[A rare familial form of idiopathic pulmonary fibrosis with Poly(A)-specific ribonuclease (PARN) mutation].

Abstract

New techniques of DNA sequences allow to discover genetics mutations involved in familial pulmonary fibrosis. Among them, the PARN (Poly[A]-specific ribonuclease) mutation. Herein, we report the case of one patient who has pulmonary fibrosis with PARN mutation and the experience of our patient care.

• Authors: M Verduyn, M Rigaud, C Dromer
• Journal: Revue de pneumologie clinique (Rev Pneumol Clin) Vol. 73 Issue 5 Pg. 272-275 (Oct 2017) ISSN: 1776-2561 [Electronic] France
• Vernacular Title: Mutation poly(A)-specific ribonuclease (PARN) et fibrose pulmonaire idiopathique familiale : à propos d’un cas au centre hospitalier universitaire de Bordeaux.
• PMID: 29055513 (Publication Type: Case Reports, Journal Article)
• Copyright: Copyright © 2017 Elsevier Masson SAS. All rights reserved.

Chemical References

• Exoribonucleases
• poly(A)-specific ribonuclease

Topics

• Exoribonucleases (genetics)
• Female
• France
• Hospitals, University
• Humans
• Idiopathic Pulmonary Fibrosis (genetics, therapy)
• Middle Aged
• Mutation