A de novo direct duplication of 9p22→p24 was shown in a child with a duplication 9p phenotype by GTG banding and fluorescence in situ hybridization (FISH) using a chromosome-9 specific painting probe as well as 6 YAC DNA probes localized to the 9p13-9p23 region. The breakpoints in this patient and p
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism
✍ Scribed by Faivre, Laurence; Viot, G�raldine; Prieur, Marguerite; Turleau, Catherine; Gosset, Philippe; Romana, Serge; Munnich, Arnold; Vekemans, Michel; Cormier-Daire, Val�rie
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 23 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(20000410)91:4<273::aid-ajmg6>3.0.co;2-h
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✦ Synopsis
We report on a child with apparent Sotos syndrome (cerebral gigantism) and partial duplication of the short arm of chromosome 20 mosaicism. Trisomy 20p11.2-p12.1 was diagnosed using cytogenetic and FISH studies. The somatostatin receptor 4 (SSTR4) gene is included in the duplicated segment. This suggests that a dosage effect of this gene might be related to some of the clinical findings observed in our patient. The present observation emphasizes the importance of chromosome analysis in patients with well-delineated but sporadic conditions.
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