Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: Clinical aspects

R. C.M. Hennekam*, M. Tilanus, B. C.J. Hamel, H. Voshart-van Heeren, E. C.M. Mariman, S. E.C. Van Beersum, M. J.H. Van den Boogaard, M. H. Breuning

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

58 Citations (Scopus)


In the accompanying paper, a chromosomal localization of the Rubinstein- Taybi syndrome by cytogenetic investigations with fluorescence in situ hybridization techniques at chromosome 16p13.3 is described. We investigated 19 of these patients and their parents (a) to ascertain the parental origin of the chromosome with the deletion in families where such a deletion was detected, (b) to disclose whether uniparental disomy plays a role in etiology, and (c) to compare clinical features in patients with a deletion to those in individuals in whom deletions were not detectable. Molecular studies showed a copy of chromosome 16 from each parent in all 19 patients. Uniparental disomy was also excluded for five other chromosome arms known to be imprinted in mice. None of the probes used for determining the origin of the deleted chromosome proved to be informative. The clinical features were essentially the same in patients with and without visible deletion, with a possible exception for the incidence of microcephaly, angulation of thumbs and halluces, and partial duplication of the halluces. A small deletion at 16p13.3 may be found in some patients with Rubinstein-Taybi syndrome. Cytogenetically undetectable deletions, point mutations, mosaicism, heterogeneity, or phenocopy by a nongenetic cause are the most probable explanations for the absence of cytogenetic or molecular abnormalities in other patients with Rubinstein-Taybi syndrome.

Original languageEnglish
Pages (from-to)255-262
Number of pages8
JournalAmerican Journal of Human Genetics
Issue number2
Publication statusPublished - 1 Jan 1993


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