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akaturk Akademik ölçüm

Makale detayı · 2025

Evaluation of Growth Characteristics and Final Height of Cases Diagnosed with Noonan Syndrome on Growth Hormone Treatment

Journal of Clinical Research in Pediatric Endocrinology

YÖKSİS OpenAlex Açık erişim · gold SJR Q2 JCR Q2 TR Index Atıf 3 Yüzdelik 61.4% FWCI 0.46
Yıl
2025
ISSN
1308-5727
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

Objective: Proportional short stature is one of the most important features of Noonan syndrome (NS), and adult height often remains below the third percentile. Although the pathophysiology of short stature in NS patients is not fully understood, it has been shown that growth hormone (GH) treatment is beneficial in NS, significantly improving height in respect to the results of short and long-term GH treatment. Methods: In this national retrospective cohort study, patients with NS who reached final height from 14 centers were evaluated. Patients were stratified by sex and treatment with or without GH and final height outcomes were compared. Results: The study included 67 patients with NS, of whom 53 (79.1%) with mean follow-up 5.6 years, received GH treatment. At presentation height standard deviation scores (SDS) of the subjects who were started on GH tended to be shorter than those who did not (-3.26±1.07 vs. -2.53±1.23). In girls mean final height and final height SDS in those using GH vs not using GH were 150.1 cm (-2.17 SDS) vs. 147.4 cm (-2.8 SDS), respectively, and for boys these values were 162.48 cm (-1.81 SDS) vs 157.46 cm (-2.68 SDS), respectively. The Δheight SDS value of the cases was significantly higher in the group receiving GH compared to those not receiving GH (1.36±1.12 SD vs. -0.2±1.24, p<0.001). Cardiac findings remained stable in two patients with hypertrophic cardiomyopathy who received GH treatment. No significant side effects were observed in any patient during follow-up. Conclusion: In patients with NS who reach their final height, a significant increase in height was observed with GH treatment. An increase of approximately +1.4 SDS may be achieved. GH treatment appears to be safe and effective in NS.

Konular

  • Protein Tyrosine Phosphatases
  • PI3K/AKT/mTOR signaling in cancer
  • Cytokine Signaling Pathways and Interactions

Birincil konu Protein Tyrosine Phosphatases

Yazarlar

  1. ZEYNEP ŞIKLAR
  2. MERİH BERBEROĞLU
  3. sirmen çetin kızılcan
  4. MELEK YILDIZ
  5. SERAP DEMİRCİOĞLU
  6. ŞÜKRAN DARCAN
  7. SEMRA ÇETİNKAYA
  8. NİHAL HATİPOĞLU
  9. ruken yıldırım
  10. KORCAN DEMİR
  11. ÖZNUR VERMEZOĞLU
  12. ZEHRA YAVAŞ ABALI
  13. DENİZ ÖZALP KIZILAY
  14. nilay görkem erdoğan
  15. ÜLKÜ GÜL ŞİRAZ
  16. ZERRİN ORBAK
  17. İLKER TOLGA ÖZGEN
  18. AYSUN BİDECİ GAZİ ÜNİVERSİTESİ
  19. BERAY SELVER EKLİOĞLU
  20. ESİN KARAKILIÇ ÖZTURAN
  21. GÜRKAN TARÇIN
  22. ABDULLAH BEREKET MARMARA ÜNİVERSİTESİ
  23. FATMA FEYZA DARENDELİLER