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Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to similar to 650 kb

Schoumans, J; Staaf, Johan LU ; Jönsson, Göran B LU ; Rantala, J; Zimmer, K S; Borg, Åke LU ; Nordenskjold, M and Anderlid, B M (2005) In European Journal of Medical Genetics 48(3). p.290-300
Abstract
Smith-Magenis syndrome (SMS) is a multiple congenital anomaly/mental retardation syndrome and it is characterized by an interstitial deletion of chromosome 17p11.2. SMS patients have a distinct phenotype which is believed to be caused by haploinsufficiency of one or more genes in the associated deleted region. Five non-deletion patients with classical phenotypic features of SMS have been reported with mutations in the retinoic acid induced I (RAII) gene, located within the SMS critical interval. Happloinsufficiency of the RAII gene is likely to be the responsible gene for the majority of the SMS features, but other deleted genes in the SMS region may modify the overall phenotype in the patients with 17p11.2 deletions. SMS is usually... (More)
Smith-Magenis syndrome (SMS) is a multiple congenital anomaly/mental retardation syndrome and it is characterized by an interstitial deletion of chromosome 17p11.2. SMS patients have a distinct phenotype which is believed to be caused by haploinsufficiency of one or more genes in the associated deleted region. Five non-deletion patients with classical phenotypic features of SMS have been reported with mutations in the retinoic acid induced I (RAII) gene, located within the SMS critical interval. Happloinsufficiency of the RAII gene is likely to be the responsible gene for the majority of the SMS features, but other deleted genes in the SMS region may modify the overall phenotype in the patients with 17p11.2 deletions. SMS is usually diagnosed in the clinical genetic setting by FISH analysis using commercially available probes. We detected a submicroscopic deletion in 17p11.2 using array-CGH with a resolution of approximately 1 Mb in a patient with the SMS phenotype, who was not deleted for the commercially available SMS microdeletion FISH probe. Delineation of the deletion was performed using a 32K tiling BAC-array, containing 32,500 BAC clones. The deletion in this patient was size mapped to 2.7 Mb and covered the RAII gene. This case enabled the refinement of the SMS minimum deletion to similar to 650 kb containing eight putative genes and one predicted gene. In addition, it demonstrates the importance to investigate deletion of RAII in SMS patients. (Less)
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author
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Smith-Magenis syndrome, array-CGH, RAI1, SMS, deletion 17p11.2
in
European Journal of Medical Genetics
volume
48
issue
3
pages
290 - 300
publisher
Elsevier
external identifiers
  • wos:000232614200008
  • scopus:25144519604
ISSN
1769-7212
DOI
10.1016/j.ejmg.2005.05.004
language
English
LU publication?
yes
id
ede9d31b-0d3c-482d-a994-02a527a8970a (old id 218822)
date added to LUP
2007-08-10 09:10:39
date last changed
2017-01-08 04:01:48
@article{ede9d31b-0d3c-482d-a994-02a527a8970a,
  abstract     = {Smith-Magenis syndrome (SMS) is a multiple congenital anomaly/mental retardation syndrome and it is characterized by an interstitial deletion of chromosome 17p11.2. SMS patients have a distinct phenotype which is believed to be caused by haploinsufficiency of one or more genes in the associated deleted region. Five non-deletion patients with classical phenotypic features of SMS have been reported with mutations in the retinoic acid induced I (RAII) gene, located within the SMS critical interval. Happloinsufficiency of the RAII gene is likely to be the responsible gene for the majority of the SMS features, but other deleted genes in the SMS region may modify the overall phenotype in the patients with 17p11.2 deletions. SMS is usually diagnosed in the clinical genetic setting by FISH analysis using commercially available probes. We detected a submicroscopic deletion in 17p11.2 using array-CGH with a resolution of approximately 1 Mb in a patient with the SMS phenotype, who was not deleted for the commercially available SMS microdeletion FISH probe. Delineation of the deletion was performed using a 32K tiling BAC-array, containing 32,500 BAC clones. The deletion in this patient was size mapped to 2.7 Mb and covered the RAII gene. This case enabled the refinement of the SMS minimum deletion to similar to 650 kb containing eight putative genes and one predicted gene. In addition, it demonstrates the importance to investigate deletion of RAII in SMS patients.},
  author       = {Schoumans, J and Staaf, Johan and Jönsson, Göran B and Rantala, J and Zimmer, K S and Borg, Åke and Nordenskjold, M and Anderlid, B M},
  issn         = {1769-7212},
  keyword      = {Smith-Magenis syndrome,array-CGH,RAI1,SMS,deletion 17p11.2},
  language     = {eng},
  number       = {3},
  pages        = {290--300},
  publisher    = {Elsevier},
  series       = {European Journal of Medical Genetics},
  title        = {Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to similar to 650 kb},
  url          = {http://dx.doi.org/10.1016/j.ejmg.2005.05.004},
  volume       = {48},
  year         = {2005},
}