Literature DB >> 30820928

Telomeropathies: Etiology, diagnosis, treatment and follow-up. Ethical and legal considerations.

Romina G Armando1, Diego L Mengual Gomez1, Julián Maggio1, María C Sanmartin1, Daniel E Gomez1.   

Abstract

Telomeropathies involve a wide variety of infrequent genetic diseases caused by mutations in the telomerase maintenance mechanism or the DNA damage response (DDR) system. They are considered a family of rare diseases that often share causes, molecular mechanisms and symptoms. Generally, these diseases are not diagnosed until the symptoms are advanced, diminishing the survival time of patients. Although several related syndromes may still be unrecognized this work describes those that are known, highlighting that because they are rare diseases, physicians should be trained in their early diagnosis. The etiology and diagnosis are discussed for each telomeropathy and the treatments when available, along with a new classification of this group of diseases. Ethical and legal issues related to this group of diseases are also considered.
© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  DNA damage response system; laminopathies; legal issues; rare diseases; telomere; telomere biology disorders; telomere maintenance; telomeropathies

Year:  2019        PMID: 30820928     DOI: 10.1111/cge.13526

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  5 in total

1.  Telomere and Centromere Staining Followed by M-FISH Improves Diagnosis of Chromosomal Instability and Its Clinical Utility.

Authors:  Radhia M'kacher; Bruno Colicchio; Claire Borie; Steffen Junker; Valentine Marquet; Leonhard Heidingsfelder; Kevin Soehnlen; Wala Najar; William M Hempel; Noufissa Oudrhiri; Nadège Wilhelm-Murer; Marguerite Miguet; Micheline Arnoux; Catherine Ferrapie; Wendy Kerbrat; Andreas Plesch; Alain Dieterlen; Theodore Girinsky; Philippe Voisin; Georges Deschenes; Anne-Claude Tabet; Catherine Yardin; Annelise Bennaceur-Griscelli; Michael Fenech; Patrice Carde; Eric Jeandidier
Journal:  Genes (Basel)       Date:  2020-04-27       Impact factor: 4.096

Review 2.  Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms.

Authors:  Megan Schmit; Anja-Katrin Bielinsky
Journal:  Int J Mol Sci       Date:  2021-01-18       Impact factor: 5.923

Review 3.  Immune Phenomena in Myeloid Neoplasms: An "Egg or Chicken" Question.

Authors:  Wilma Barcellini; Bruno Fattizzo
Journal:  Front Immunol       Date:  2021-09-29       Impact factor: 7.561

4.  Patient-Derived iPSCs Reveal Evidence of Telomere Instability and DNA Repair Deficiency in Coats Plus Syndrome.

Authors:  Noufissa Oudrhiri; Radhia M'kacher; Diana Chaker; Bruno Colicchio; Claire Borie; Eric Jeandidier; Alain Dieterlen; Frank Griscelli; Annelise Bennaceur-Griscelli; Ali G Turhan
Journal:  Genes (Basel)       Date:  2022-08-05       Impact factor: 4.141

Review 5.  Effector immune cells in chronic lung allograft dysfunction: A systematic review.

Authors:  Saskia Bos; Andrew J Filby; Robin Vos; Andrew J Fisher
Journal:  Immunology       Date:  2022-03-01       Impact factor: 7.215

  5 in total

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