Telomeres: A diagnosis at the end of the chromosomes

BBA de Vries*, R Winter, A Schinzel, C van Ravenswaaij-Arts

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

202 Citations (Scopus)

Abstract

In recent years, subtelomeric rearrangements have been identified as a major cause of mental retardation and/or malformation syndromes. So far, over 2500 subjects with mental retardation have been tested and reported of whom similar to5% appeared to have a subtelomeric rearrangement.

In this review, the clinical aspects of each known (submicroscopic) subtelomeric deletion will be presented and the various methods available for detecting subtelomeric abnormalities will be discussed. Not only will the patients and their families benefit from a good collection and report of the various telomeric abnormalities and their clinical phenotype, but it will also give more insight into the aetiology of mental retardation and malformation syndromes.

Original languageEnglish
Pages (from-to)385-398
Number of pages14
JournalJournal of Medical Genetics
Volume40
Issue number6
DOIs
Publication statusPublished - Jun-2003
Externally publishedYes

Keywords

  • IDIOPATHIC MENTAL-RETARDATION
  • ALBRIGHT HEREDITARY OSTEODYSTROPHY
  • DIAMOND-BLACKFAN ANEMIA
  • MILLER-DIEKER-SYNDROME
  • FAMILIAL CRYPTIC TRANSLOCATION
  • WOLF-HIRSCHHORN-SYNDROME
  • IN-SITU HYBRIDIZATION
  • COMPARATIVE GENOMIC HYBRIDIZATION
  • SILVER-RUSSELL SYNDROME
  • REGION-SPECIFIC PROBES

Fingerprint

Dive into the research topics of 'Telomeres: A diagnosis at the end of the chromosomes'. Together they form a unique fingerprint.

Cite this