Journals / Tıp Araştırmaları Dergisi / 2013 / Cilt: 11 - Sayı: 1

Case with Crouzon Syndrome

Crouzon Sendromu: Bir Olgu Sunumu

Pages
40–42
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

We reported this case which was diagnosed as Crouzon syndrome by characteristic phenotypic features and imagin studies as it rarely seen.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:A 10 years old girl who presented with respiratory distress and vomiting and admitted to pediatric intensive care unit had dysmorphic features.
📊
Key Findings & Data:A 10 years old girl who presented with respiratory distress and vomiting and admitted to pediatric intensive care unit had dysmorphic features.
💡
Conclusion & Impact:We reported this case which was diagnosed as Crouzon syndrome by characteristic phenotypic features and imagin studies as it rarely seen.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

A 10 years old girl who presented with respiratory distress and vomiting and admitted to pediatric intensive care unit had dysmorphic features. We reported this case which was diagnosed as Crouzon syndrome by characteristic phenotypic features and imagin studies as it rarely seen.

Özet

Solunum sıkıntısı ve kusma şikayetiyle getirilen büyüme gelişme geriliği ve pnömoni tanısıyla çocuk yoğun bakım ünitesine yatırılan 10 yaşında kız çocuk dismorl'ık özelliklere sahipti. Karakteristik fenotipik özellikleri ve görüntüleme yöntemleriyle Crouzon sendromu tanısı koyduğumuz olguyu nadir rastlanması nedeniyle sunduk.

🔖

Cite This Article

DOĞAN, M., KABA, S., BULAN, K., DOĞAN, Ş. Z., DEMİR, N., ÜSTYOL, L. (2013). Case with Crouzon Syndrome. Tıp Araştırmaları Dergisi, Cilt: 11 - Sayı: 1, 40–42. https://ajindex.com/articles/361893

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Locuratolo N, Baffico M, Baldi M, Parisi V, Micacchi F, Angelucci V, Rojas Beccaglia M, Pirro C, Fattapposta F. novel fibroblast growtth faktör receptor (FGFRZ) mutation associated with mild Crouzon syndrome. Arch Ital Biol. 2011;149:313-7 (pubmed
  2. Haslam RHA. Neurologic Evaluation, Craniosynostosis: In. Nelson Textbook of Pediatrics 17th ed. Philadelphia: WB Saunders, 2004:1992-1993 3. Hobelt CV. Physical and oral characteristics of Crouzon syndrome, Apert syndrome,and Pierre Robin sequence.Gen Dent.2008;5 6: 32- 4.(PubMed
  3. Murano I. Crouzon syndrome. Nihon Rinsho. 2006; (Suppl 3):416-7.(Pubmed
  4. Ahmed I, Afzal A. Diagnosis and evaluation of Crouzon syndromeç Coll Physicians Surg Pak. 2009;19:318-20. (Pubmed
  5. Smith DW. Recognizable Patterns of Human Malformation Genetic, Embryologic and Clinical Aspaects 3rd ed. Philadelphia: WB Saunders, l982:3lO-ll
  6. Al-Qattan MM, Philips JH. Clinical features of Crouzon's syndrome patients withand without positive family history of Crouzon syndrome. Craniofac Surg 1997;8211-3
  7. Proudman TW, Moore MH, Abbott AH, David DJ. Noncraniofacial manifestations of Crouzon's disease. Craniofac Surg 199;5:218-22
  8. Acrocephalopolysyndactyly (Typ McKusick) acrocephalosyndactyly or Carpenter's Syndrome). Report on cases and an observation of Syndromeof Marshall-Smith. Klin Pediatr 1997;189:120-30
  9. Pissuan C, Van poperinghe M, Grumbach Y, Audbert M, Helsema C, Risbourg B. Carpenter's Syndrome. Arch Fr Pediatr l997;34:89l-898.