CHARGE sendromu tanısı alan 2 aylık bir bebek

CHARGE sendromu patogenetik olarak ilintili konjenital anomalilerden oluşan ve 6 ana klinik özelliği bulunan nadir bir sendromdur. Burada hastanemize doğumsal kalp anomalilerinin (aort koarktasyonu, biküspid aortik kapak ve patent duktus arteriosus) cerrahi olarak düzeltilmesi için kabul edilen bir kız olguyu sunduk. Olgumuzun kalp anomalisine ek olarak bilateral optik disk ve koroid kolobomu, opere edilmiş çift taraflı koanal atrezisi, sağ fasiyal paralizisi, kulak anomalisi ve büyüme geriliği mevcuttu. Bu bulgularla hastamıza CHARGE sendromu tanısını koyduk. CHARGE sendromlu çocuklar çoklu cerrahi girişimlere ihtiyaç duydukları ve annenin sonraki gebeliklerinde de konjenital anomalili bebek riski arttığı için bu sendromu erken tanımak, aileyi bilgilendirmek ve genetik danışmanlık vermek oldukça önemlidir. Eşlik eden koanal atrezi ve kardiyak anomaliler gibi konjenital malformasyonlara erken müdahele etmek hayat kurtarıcı olacaktır. Bu nedenle, CHARGE sendromunu literatür eşliğinde yeniden hatırlatmak istedik.
Anahtar Kelimeler:

Doğumsal, Çoklu anomali, CHARGE

-

CHARGE is a rare syndrome characterized by association of pathogenetically related multiple congenital anomalies with six main clinical features. In this case report, we present a 2-month-old female baby admitted to our hospital for surgical correction of her congenital heart anomalies (aortic coarctation, bicuspid aortic valve and patent ductus arteriosus). In addition, she had bilateral optic disc and choroid colobomas, operated bilateral choanal atresia, right facial nerve paralysis, ear anomaly and growth retardation to make the diagnosis of CHARGE syndrome. As children with CHARGE require multiple surgical corrections and the risk of congenital anomalies increases in subsequent pregnancies, it is important to recognize and inform the family about this syndrome as soon as possible. Early interventions for correction of accompanying congenital anomalies like choanal atresia can be life saving. Therefore, we wanted to highlight CHARGE syndrome and review the relevant literature

___

  • 1. Graham Jr JM. A recognizable syndrome within CHARGE association. Hall-Hittner syndrome. Am J Med Genet 2001; 99:120–3. doi:10.1002/1096-8628(2000)
  • 2. Pagon RA, Graham Jr JM, Zonana JY, Young SL. Coloboma, congenital heart disease, and choanal atresia with multiple anomalies. CHARGE association. J Pediat 1981; 99:223–7. doi:10.1016/S0022- 3476(81)80454-4
  • 3. Lubinsky MS. Properties of associations. Identity, nature, and clinical criteria, with a commentary on why CHARGE and Goldenhar are not associations. Am J Med Genet 1994; 49:21–5. doi:10.1002/ ajmg.1320490106
  • 4. Allouche C, Sarda P. The CHARGE association. Pediatrie 1989; 44:391-5.
  • 5. Blake KD, Prasad C. CHARGE syndrome. Orphanet Journal of Rare Diseases 2006 Sep 7; 1:34. Review.
  • 6. Clementi M, Tenconi R. Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome. Am J Med Genet 1991; 41: 246-50.
  • 7. Tellier AL, Cormier-Daire V, Abadie V, et al. CHARGE syndrome:report of 47 cases and review. Am J Med Genet 1998; 76: 402–9.
  • 8. Blake KD, Davenport SLH, Hall BD, et al. CHARGE association: an update and review for the primary pediatrician. Clin Pediatr (Phila) 1998;37:159-73. doi:10.1177/000992289803700302
  • 9. Davenport SLH, Hefner MA, Mitchell JA. The spectrum of clinical features in CHARGE syndrome. Clin Genet 1986; 29:298-310. doi:10.1111/j.1399-0004.1986.tb01258.x
  • 10. İrdem A, Başpınar O, Kervancıoğlu M, Kılınç M. CHARGE syndrome together with middle aortic syndrome. Gaziantep Med J 2012; 18:109- 12.
  • 11. Leitch CA. Growth, nutrition and energy expenditure in pediatric heart failure. Prog Pediatr Cardiol 2000;11:195-202.
  • 12. Searle L, Blake KD. CHARGE syndrome from birth to adulthood:an individual reported from 0 to 33 years. Am J Med Genet A 2005;133:344-9. doi:10.1002/ajmg.a.30565
  • 13. Stromland K, Sjogreen L, Johansson M, et al. CHARGE association in Sweden: malformations and functional deficits. Am J Med Genet A 2005; 133:331–9. doi:10.1002/ajmg.a.30563
  • 14. Lalani SR, Safiullah AM, Fernbach SD, Harutyunyan KG. Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation. Am J Hum Genet 2006;78:303-14. doi:10.1086/500273
  • 15. Emanuel BS, Budarf ML, Sellinger B, Goldmuntz E, Driscoll DA. Detection of microdeletions of 22q11.2 with fluorescence in situ hybridization (FISH): diagnosis of DiGeorge (DGS),velo-cardiofacial (VCF) syndrome, CHARGE association and conotruncal cardiac malformations. Am J Hum Genet 1992;51 (Suppl):A3.
  • 16. Lalani SR, Safiullah AM, Molinari LM, Fernbach SD, Martin DM, Belmont JW. SEMA3E mutation in a patient with CHARGE syndrome. J Med Genet 2004; 41: e94. doi:10.1136/jmg.2003.017640
  • 17. Tellier AL, Lyonnet S, Cormier-Daire V, et al. Increased paternal age in CHARGE association. Clin Genet 1996;50:548-50.
  • 18. Becker R, Stiemer B, Neumann L, Entezami M. Mild ventriculomegaly, mild cerebellar hypoplasia and dysplastic choroid plexus as early prenatal signs of CHARGE association. Fetal Diagn Ther 2001;16:280- 3. doi: 10.1159/000053928
  • 19. Sanlaville D, Etchevers HC, Gonzales M, et al. Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development. J Med Genet 2006; 43:211-7. doi:10.1136/jmg.2005.036160
  • 20. Bergman J, Janssen N, Hoefsloot. L.CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype. J Med Genet 2011; 48:334-42. doi:10.1136/jmg.2010.087106
Marmara Medical Journal-Cover
  • ISSN: 1019-1941
  • Yayın Aralığı: Yılda 3 Sayı
  • Başlangıç: 1988
  • Yayıncı: Marmara Üniversitesi