Genetic Counseling and Family Screening Recommendations in Patients with Telomere Biology Disorders

Curr Hematol Malig Rep. 2023 Dec;18(6):273-283. doi: 10.1007/s11899-023-00713-8. Epub 2023 Oct 3.

Abstract

Purpose of review: Telomere biology disorders (TBDs) encompass a spectrum of genetic diseases with a common pathogenesis of defects in telomerase function and telomere maintenance causing extremely short telomere lengths. Here, we review the current literature surrounding genetic testing strategies, cascade testing, reproductive implications, and the role of genetic counseling.

Recent findings: The understanding of the genetic causes and clinical symptoms of TBDs continues to expand while genetic testing and telomere length testing are nuanced tools utilized in the diagnosis of this condition. Access to genetic counseling is becoming more abundant and is valuable in supporting patients and their families in making informed decisions. Patient resources and support groups are valuable to this community. Defining which populations should be offered genetic counseling and testing is imperative to provide proper diagnoses and medical management for not only the primary patient, but also their biological relatives.

Keywords: Dyskeratosis congenita; Genetic counseling; Genetic testing; Short telomere syndrome; Telomere biology disorder (TBD).

Publication types

  • Review

MeSH terms

  • Genetic Counseling*
  • Genetic Testing
  • Humans
  • Mutation
  • Telomerase* / genetics
  • Telomerase* / metabolism
  • Telomere / genetics
  • Telomere / metabolism

Substances

  • Telomerase