TY - JOUR
T1 - Telomeres
T2 - A diagnosis at the end of the chromosomes
AU - de Vries, BBA
AU - Winter, R
AU - Schinzel, A
AU - van Ravenswaaij-Arts, C
PY - 2003/6
Y1 - 2003/6
N2 - 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.
AB - 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.
KW - IDIOPATHIC MENTAL-RETARDATION
KW - ALBRIGHT HEREDITARY OSTEODYSTROPHY
KW - DIAMOND-BLACKFAN ANEMIA
KW - MILLER-DIEKER-SYNDROME
KW - FAMILIAL CRYPTIC TRANSLOCATION
KW - WOLF-HIRSCHHORN-SYNDROME
KW - IN-SITU HYBRIDIZATION
KW - COMPARATIVE GENOMIC HYBRIDIZATION
KW - SILVER-RUSSELL SYNDROME
KW - REGION-SPECIFIC PROBES
U2 - 10.1136/jmg.40.6.385
DO - 10.1136/jmg.40.6.385
M3 - Review article
SN - 0022-2593
VL - 40
SP - 385
EP - 398
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
IS - 6
ER -