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Journals / Medical Network Klinik Bilimler ve Doktor / 2004 / Cilt: 10 - Sayı: 4

Noonan syndrome with tricuspid atresia

Noonan sendromlu bir olguda triküspit atrezisi

Nursel ALPAN
Hasan Tahsin ÇAKIR
BAHAR ÇUHACI ÇAKIR
Kutay SEL
Pages
434–437
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The prevalence of congenital heart defect in Noonan syndrome varies from 50 to 80%, however pulmonary stenosis and hypertrophic cardiomyopathy are generally the most common congenital heart defects found in Noonan syndrome.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The prevalence of congenital heart defect in Noonan syndrome varies from 50 to 80%, however pulmonary stenosis and hypertrophic cardiomyopathy are generally the most common congenital heart defects found in Noonan syndrome.
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Key Findings & Data:The prevalence of congenital heart defect in Noonan syndrome varies from 50 to 80%, however pulmonary stenosis and hypertrophic cardiomyopathy are generally the most common congenital heart defects found in Noonan syndrome.
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Conclusion & Impact:The prevalence of congenital heart defect in Noonan syndrome varies from 50 to 80%, however pulmonary stenosis and hypertrophic cardiomyopathy are generally the most common congenital heart defects found in Noonan syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Triküspit atrezi · Noonan sendromu · Tricuspid Atresia

Abstract

The prevalence of congenital heart defect in Noonan syndrome varies from 50 to 80%, however pulmonary stenosis and hypertrophic cardiomyopathy are generally the most common congenital heart defects found in Noonan syndrome.

Özet

Noonan sendromunda %50-80 oranında kalp hastalıkları görülürken, en sık saptanan kardiyak anomaliler pulmoner stenoz ve hipertrofik kardiyomiyopatidir. Noonan sendromu ile triküspid atrezisi literatürde hiç bildirilmemiş olması nedeniyle sunulmuştur.

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Cite This Article

ALPAN, N., ÇAKIR, H. T., ÇAKIR, B. Ç., SEL, K. (2004). Noonan syndrome with tricuspid atresia. Medical Network Klinik Bilimler ve Doktor, Cilt: 10 - Sayı: 4, 434–437. https://ajindex.com/articles/278468

References (14)

  1. Burch M, Sharland M, Shinebourne E, et al. Cardiologic abn( malities in Noonan syndrome: phenotypic abnormalities in Noon; syndrome: phenotypic diagnosis and echocardiographic a sessment in 119 patients, J Am Coll Cardiol, 1993; 22:1189-92.
  2. Jamieson CR, Van der Burgt I, Brady AF, et al. Mapping agene for Noonan syndrome to the long arm of chromosome 1 Nat Genet, 1994; 8:357-60.
  3. Sharland M, Burch M, McKenna WM, et al. A clinical study Noonan syndrome, Arch Dis Child, 1992; 67:178-83.
  4. Shukla OP, Chandwani R, Om Prakash Shukla, et al. Noonan Syndrome, Indian Journal of Clinical Practice, 200 12:39-40.
  5. Van der Burgt I, Thoonet G, Roosenboom N, et al. Patterns of cognitive functioning in school- aged children with Noon* idrome associated with variability in phenotypic expression, J Şiatr, 1999; 135:707-13.
  6. Marino B, Digilio MC, Toscano A. Congenital heart diseases "children with Noonan syndrome: An expanded cardiac ectrum with high prevalence of atrioventricular canal, J idiatr, 1999; 135:703-6.
  7. Bgrch M, Sharland M, Mckenna WM, et al. A clinical study of jonan syndrome, Arch Dis Child, 1992; 67:178-83.
  8. Ishikawa Y, Sekiguchi K, Akasaka Y, et al. Fibromuscular splasia of coronary arteries resulting in myocardial infarction isociated with hypertrophic cardiomyopathy in Noonan's ndrome, Hum Pathol, 2003; 34:282-4.
  9. Marino B, Gagliardi MG, Digilio MC, et al. Noonan syndrome: ructural abnormalities of the mitral valve causing subaortic îstruction, Eur J Pediatr, 1995; 154:949-52.
  10. Digilio MC, Marino B, Picchio F, et al. Noonan syndrome and aortic coarctation, Am J Med Genet, 1998; 80:160-2.
  11. Digilio MC, Marino B. Clinical manifestations of Noonan syndrome, Images Paediatr Cardiol, 2001; 7:19-30.
  12. Tutar E, Arslan S, Kuzu I, Atalay S, Atasay B, Gençgönül H. Dismorfik Bulguları Olan Bir Yenidoğanda Hipertrofik Kardiyomiyo- pati: Noonan Sendromu, Türk Kardiyol Dern Arş, 1999; 27:59-62.
  13. Özkutlu S, Çil E, Paşaoğlu I, Saraçlar M. Noonan syndrome with double-chambered right ventricle, Pediatr Cardiol, 1996; 17:251-3.
  14. Bertola DR, Chang AE, Sugayama SMM, et al. Cardiac findings in 31 patients with Noonan's syndrome, Arq Bras Cardiol, 2000; 75:409-12.