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A CASE REPORT: GOLDENHAR’S SYNDROME

Yıl 2010, Cilt: 1 Sayı: 3, - , 03.03.2015

Öz

Oculo-auriculo-vertebral spectrum (OAVS), also known as Goldenhar's syndrome, involves often congenital defects in the first and second branchial arches. The incidence of Goldenhar’s syndrome has been reported to be ranged from 1:3500 to 1:5600. Goldenhar's syndrome is characterized as a disease which is accompanied by craniofacial abnormalities, cardiovascular, genitourinary and vertebral anomalies. Despite the manifestation of different chromosome abnormalities and inheritance patterns in Goldenhar's syndrome, most patients have no chromosomal abnormalities. This paper describes clinical and laboratory findings of a boy case aged 50 days with complaints of respiratory distress and difficulty of absorption from birth, and diagnosed with Goldenhar’s syndrome and emphasize crucial points to be considered in the following-up.

Kaynakça

  • Greenberg F, Herman GE, Stal S, Gruber H, Ledbetter DH. Chromosome abnormalities associated with facioauriculo- vertebral spectrum. Am J Med Genet Suppl 1988; 4A(Suppl):
  • Rollnick BR. Oculoauriculovertebral anomaly: variability and causal heterogeneity. Am J Med Genet Suppl 1988; 4: 41-53.
  • Gorlin RJ, Cohen MM, Levin LS. Brachial arch and oroacral disorders. In: Syndromes of the Head and Neck, (2nd ed). Newyork: Oxford University Press 1990: 641- 9.
  • Hermann, J. and Opitz, J. M.: A dominently inherited first arch syndrome. Birth Defects ; 5: 110-2
  • McKenzie, J. The first arch syndrome. Arch. Dis. Childh.1958; 33: 477-86
  • Opitz JM. Developmental field theory and observationsaccidental progress? Am J Med Genet 1986; 2(Suppl): 1-9.
  • Russell LJ, Weaver DD, Bull MJ. The axial mesodermal dysplasia spectrum. Pediatrics ; 67: 176-82. Saraçlar M, Friedman S. Congenital cardiac anomalies in Goldenhar’s syndrome. 1974; 16: 9.
  • Morrison PJ, Mulholland HC, Craig BG, Nevin NC. Cardiovascular abnormalities in the oculo-auriculovertebral spectrum (Goldenhar syndrome). Am J Med Genet 1992; 44: 425-8.
  • Collins, E. T.: Cases with symmetrical congenital notches in the outer part of each lid and defective development of the malar bones. Trans. Ophthalmol. Soc. U.K., 1900; 20: 190,
  • Quoted by Salmon and Lindenbaum (1978).
  • Salmon, M. A. and Lindenbaum, R. H.: "Developmental Defects and Syndromes." H. M. + M. Publishers, London 1978; p. 40.
  • Summit, R.: Familial Goldenhar Syndrome: Birth Defects 1969; 5: 106-9.
  • Dennison, W. M.: The Pierre-Robin syndrome. Paediatrics 1965; 36: 336-41.

GOLDENHAR SENDROMLU BIR OLGU SUNUMU

Yıl 2010, Cilt: 1 Sayı: 3, - , 03.03.2015

Öz

Oculo-auriculo-vertebral spektrum (OAVS) olarak da bilinen Goldenhar’s sendromu birinci ve ikinci brankiyal arkdan gelişen yapıların sık görülen konjenital defektlerinden oluşur. Bu sendromun ortalama görülme sıklığı 1/3500 ile 1/5600 arasında olduğu bildirilmiştir. Goldenhar’s sendromu, kraniyofasiyal anomaliler, kardiyovasküler, genitoüriner ve vertebra anomalilerin eşlik etmesi ile karakterize bir sendromdur. Goldenhar’s sendromunun farklı kromozom anomalileri ve kalıtım şekilleri bildirilmesine rağmen hastaların çoğunda herhangi bir kromozom anomalisi bulunmamaktadır. Bu yazıda doğumdan itibaren, solunum sıkıntısı ve emmede zorlanma şikayetleri ile başvuran ve Goldenhar’s sendromu tanısı alan 50 günlük erkek hastanın klinik ve laboratuar bulguları gözden geçirilerek izlemde dikkat edilmesi gereken noktalar vurgulandı.

Anahtar Kelimeler: Goldenhar’s sendromu, oculo-auriculo-vertebral spektrum, kraniyofasiyal anomaliler, kardiak defekt.

Kaynakça

  • Greenberg F, Herman GE, Stal S, Gruber H, Ledbetter DH. Chromosome abnormalities associated with facioauriculo- vertebral spectrum. Am J Med Genet Suppl 1988; 4A(Suppl):
  • Rollnick BR. Oculoauriculovertebral anomaly: variability and causal heterogeneity. Am J Med Genet Suppl 1988; 4: 41-53.
  • Gorlin RJ, Cohen MM, Levin LS. Brachial arch and oroacral disorders. In: Syndromes of the Head and Neck, (2nd ed). Newyork: Oxford University Press 1990: 641- 9.
  • Hermann, J. and Opitz, J. M.: A dominently inherited first arch syndrome. Birth Defects ; 5: 110-2
  • McKenzie, J. The first arch syndrome. Arch. Dis. Childh.1958; 33: 477-86
  • Opitz JM. Developmental field theory and observationsaccidental progress? Am J Med Genet 1986; 2(Suppl): 1-9.
  • Russell LJ, Weaver DD, Bull MJ. The axial mesodermal dysplasia spectrum. Pediatrics ; 67: 176-82. Saraçlar M, Friedman S. Congenital cardiac anomalies in Goldenhar’s syndrome. 1974; 16: 9.
  • Morrison PJ, Mulholland HC, Craig BG, Nevin NC. Cardiovascular abnormalities in the oculo-auriculovertebral spectrum (Goldenhar syndrome). Am J Med Genet 1992; 44: 425-8.
  • Collins, E. T.: Cases with symmetrical congenital notches in the outer part of each lid and defective development of the malar bones. Trans. Ophthalmol. Soc. U.K., 1900; 20: 190,
  • Quoted by Salmon and Lindenbaum (1978).
  • Salmon, M. A. and Lindenbaum, R. H.: "Developmental Defects and Syndromes." H. M. + M. Publishers, London 1978; p. 40.
  • Summit, R.: Familial Goldenhar Syndrome: Birth Defects 1969; 5: 106-9.
  • Dennison, W. M.: The Pierre-Robin syndrome. Paediatrics 1965; 36: 336-41.
Toplam 13 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm Case Report
Yazarlar

Ayfer Pirinççioğlu Bu kişi benim

Halil Kocamaz Bu kişi benim

Ali Güneş Bu kişi benim

Servet Yel Bu kişi benim

Murat Tutanç Bu kişi benim

Fuat Gürkan Bu kişi benim

Yayımlanma Tarihi 3 Mart 2015
Gönderilme Tarihi 28 Şubat 2015
Yayımlandığı Sayı Yıl 2010 Cilt: 1 Sayı: 3

Kaynak Göster

Vancouver Pirinççioğlu A, Kocamaz H, Güneş A, Yel S, Tutanç M, Gürkan F. GOLDENHAR SENDROMLU BIR OLGU SUNUMU. mkutfd. 2015;1(3).