BibTex RIS Kaynak Göster

Smith-Magenis Sendrom’lu Bir Olgu

Yıl 2018, Cilt: 7 Sayı: 2, 63 - 65, 01.10.2018

Öz

Smith-Magenis senromu SMS fasiyal dismorfizm, gelişim basamaklarında gecikme, bilişsel gerilik, karakteristik davranış paterni ve uyku bozuklukları ile karakterize genetik bir hastalıktır. Bu olgu sunumunda fasiyal dismorfizm, gelişimsel gecikme ve bilişsel gerilik nedeni ile SMS tanısı alan bir olgu sunulmuştur.

Kaynakça

  • Potocki L, Shaw CJ, Stankiewicz P, et al. Variability in clinical phenotype despite common chromosomal deletion in Smith- Magenis syndrome [del(17)(p11.2p11.2)]. Genet Med 2003; 5(6): 430-4.
  • Edelman EA, Girirajan S, Finucane B, et al. Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases. Clin Genet 2007; 71(6): 540-50.
  • Vilboux T, Ciccone C, Blancato JK, et al. Molecular analysis of the Retinoic Acid Induced 1 gene (RAI1) in patients with suspected Smith- Magenis syndrome without the 17p11.2 deletion. PLoS One 2011; 6(8): e22861.
  • Greenberg F, Guzzetta V, Montes de Oca-Luna R, et al. Molecular analysis of the Smith- Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2). Am J Hum Genet 1991; 49(6): 1207-18.
  • Williams SR, Zies D, Mullegama SV, et al. Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity. Am J Hum Genet 2012; 90(6): 941-9.
  • Laje G, Bernert R, Morse R, et al. Pharmacological treatment of disruptive behavior in Smith-Magenis syndrome. Am J Med Genet C Semin Med Genet 2010; 154C(4): 463-8.
  • De Leersnyder H, De Blois MC, Claustrat B, et al. Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome. J Pediatr 2001; 139(1): 111-6.
  • De Leersnyder H, Bresson JL, de Blois MC, et al. "Beta 1-adrenergic antagonists and melatonin reset the clock and restore sleep in a circadian disorder, Smith-Magenis syndrome." J Med Genet 2003; 40(1): 74-8.
  • Zori RT, Lupski JR, Heju Z, et al. Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion. Am J Med Genet 1993; 47(4): 504-11.

A Case of Smith-Magenis Syndrome

Yıl 2018, Cilt: 7 Sayı: 2, 63 - 65, 01.10.2018

Öz

Smith-Magenis syndrome is a genetic disorder characterized by facial dysmorphism, developmental delay, cognitive retardation, characteristic behavior pattern and sleep disturbance. In this study we report a Smith Magenis Syndrome patient with facial dysmorphism, developmental delay and cognitive retardation.

Kaynakça

  • Potocki L, Shaw CJ, Stankiewicz P, et al. Variability in clinical phenotype despite common chromosomal deletion in Smith- Magenis syndrome [del(17)(p11.2p11.2)]. Genet Med 2003; 5(6): 430-4.
  • Edelman EA, Girirajan S, Finucane B, et al. Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases. Clin Genet 2007; 71(6): 540-50.
  • Vilboux T, Ciccone C, Blancato JK, et al. Molecular analysis of the Retinoic Acid Induced 1 gene (RAI1) in patients with suspected Smith- Magenis syndrome without the 17p11.2 deletion. PLoS One 2011; 6(8): e22861.
  • Greenberg F, Guzzetta V, Montes de Oca-Luna R, et al. Molecular analysis of the Smith- Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2). Am J Hum Genet 1991; 49(6): 1207-18.
  • Williams SR, Zies D, Mullegama SV, et al. Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity. Am J Hum Genet 2012; 90(6): 941-9.
  • Laje G, Bernert R, Morse R, et al. Pharmacological treatment of disruptive behavior in Smith-Magenis syndrome. Am J Med Genet C Semin Med Genet 2010; 154C(4): 463-8.
  • De Leersnyder H, De Blois MC, Claustrat B, et al. Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome. J Pediatr 2001; 139(1): 111-6.
  • De Leersnyder H, Bresson JL, de Blois MC, et al. "Beta 1-adrenergic antagonists and melatonin reset the clock and restore sleep in a circadian disorder, Smith-Magenis syndrome." J Med Genet 2003; 40(1): 74-8.
  • Zori RT, Lupski JR, Heju Z, et al. Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion. Am J Med Genet 1993; 47(4): 504-11.
Toplam 9 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Olgu Sunumu
Yazarlar

Zeynep Esener Bu kişi benim

İbrahim Tekedereli Bu kişi benim

Yayımlanma Tarihi 1 Ekim 2018
Yayımlandığı Sayı Yıl 2018 Cilt: 7 Sayı: 2

Kaynak Göster

APA Esener, Z., & Tekedereli, İ. (2018). Smith-Magenis Sendrom’lu Bir Olgu. Annals of Health Sciences Research, 7(2), 63-65.
AMA Esener Z, Tekedereli İ. Smith-Magenis Sendrom’lu Bir Olgu. Ann Health Sci Res. Ekim 2018;7(2):63-65.
Chicago Esener, Zeynep, ve İbrahim Tekedereli. “Smith-Magenis Sendrom’lu Bir Olgu”. Annals of Health Sciences Research 7, sy. 2 (Ekim 2018): 63-65.
EndNote Esener Z, Tekedereli İ (01 Ekim 2018) Smith-Magenis Sendrom’lu Bir Olgu. Annals of Health Sciences Research 7 2 63–65.
IEEE Z. Esener ve İ. Tekedereli, “Smith-Magenis Sendrom’lu Bir Olgu”, Ann Health Sci Res, c. 7, sy. 2, ss. 63–65, 2018.
ISNAD Esener, Zeynep - Tekedereli, İbrahim. “Smith-Magenis Sendrom’lu Bir Olgu”. Annals of Health Sciences Research 7/2 (Ekim 2018), 63-65.
JAMA Esener Z, Tekedereli İ. Smith-Magenis Sendrom’lu Bir Olgu. Ann Health Sci Res. 2018;7:63–65.
MLA Esener, Zeynep ve İbrahim Tekedereli. “Smith-Magenis Sendrom’lu Bir Olgu”. Annals of Health Sciences Research, c. 7, sy. 2, 2018, ss. 63-65.
Vancouver Esener Z, Tekedereli İ. Smith-Magenis Sendrom’lu Bir Olgu. Ann Health Sci Res. 2018;7(2):63-5.