Journals / Perinatoloji Dergisi / 2004 / Cilt: 12 - Sayı: 3

The place of prenatal ultrasound, postmortem radiography and autopsy examination in prenatal diagnosis of osteogenesis imperfecta type 2 - A case report

Osteogenesis imperfekta tip II'nin tanısında prenatal ultrason, postmortem radyografi ve otopsinin yeri - Olgu sunumu

Pages
155–160
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)

Conclusion: It is important the differantial diagnosis of osteogenesis imperfecta from other skelatal dysplasias which characterized by mineralization defect and it should be performed postmortem radiologic and autopsy investigations.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background: To discuss the differential diagnosis of ostegenesis imperfecta from other skelatal dysplasias which is characterized by mineralization defect and to emphasize the importance of postmortem radiography and autopsy findings.
📊
Key Findings & Data:Case: Twenty five -years- old patient gravida 2 para 1 33 weeks of pregnancy, refered to our clinic from another center with a diagnosis of skeletal dysplasia.
💡
Conclusion & Impact:Conclusion: It is important the differantial diagnosis of osteogenesis imperfecta from other skelatal dysplasias which characterized by mineralization defect and it should be performed postmortem radiologic and autopsy investigations.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Tanı teknik ve işlemleri · Otopsi · Tanı

Abstract

Background: To discuss the differential diagnosis of ostegenesis imperfecta from other skelatal dysplasias which is characterized by mineralization defect and to emphasize the importance of postmortem radiography and autopsy findings. Case: Twenty five -years- old patient gravida 2 para 1 33 weeks of pregnancy, refered to our clinic from another center with a diagnosis of skeletal dysplasia. Sonographic evaluation revealed that all long bones were short, depressed skull bones with transducer pressure, multipl fractures in?at the humerus and polyhydramnios. After consultation of the parents about diagnosis, pregnancy was terminated. The diagnosis was confirmed with postmortem radiologic findings and autopsy examination. Conclusion: It is important the differantial diagnosis of osteogenesis imperfecta from other skelatal dysplasias which characterized by mineralization defect and it should be performed postmortem radiologic and autopsy investigations.

Özet

Amaç: Ölümcül bir iskelet displazisi olan osteogenezis imperfektanın, diğer mineralizasyon kusuruyla giden iskelet displazilerinden ayırıcı tanısını irdelemek ve tanıda ultrasonografi ile birlikte postmortem radyografi ve otopsi bulgularının önemini vurgulamak. Olgular: 33. gebelik haftasında, G2 P1, 25 yaşında hasta, iskelet displazisi ön tanısıyla bir başka merkezden servisimize refere edildi. Yapılan ultrasonografi tüm uzun kemiklerde kısalık, kafa kemiklerinde prob baskısıyla çökme, humerusta birden çok kırık ve polihidramniyos olduğunu gösterdi. Aileye prognoz hakkında bilgi verildikten sonra gebelik sonlandırıldı. Postmortem radyografi ve otopsi bulguları ile osteogenezis imperfekta tanısı konfirme edildi. Sonuç: Osteogenezis imperfektanın diğer mineralizasyon defekti ile seyreden hastalıklardan ayırıcı tanısı önemlidir ve bu amaçla mutlaka postmortem radyografi ve otopsi incelemesi yapılmalıdır. .

🔖

Cite This Article

BAYTUR, B. Y., NEŞE, N., UYAR, Y., LAÇİN, S., İNCEBOZ, S. Ü., ÇAĞLAR, H. (2004). The place of prenatal ultrasound, postmortem radiography and autopsy examination in prenatal diagnosis of osteogenesis imperfecta type 2 - A case report. Perinatoloji Dergisi, Cilt: 12 - Sayı: 3, 155–160. https://ajindex.com/articles/300402

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. 1]. Pilu G, Nicholaides KH. Diagnosis of fetal abnormalities The 18-23 week scan. London, Parthenon, 1999; 91-2 [2]. Rumack CM, Wilson SR, Charboneau JW. Diagnostic Ultrasound Vol 2. New York,Mosby, 1997; 1214-7 [3]. Goldstein DJ, Nichols WC, Mirkin LD. Short-limbed osteochondrodysplasi with osteochondral spurs of knee and elbow joints (spur-limbed dwarfism). Dysmorph Clin Genet 1987; 1: 12-6 [4]. Kousseff BG, Mulivor RA. Prenatal diagnosis of hypophosphatasia. Obstet Gynecol 1981; 57: 9-12 [5]. Bowerman RA. Anomalies of the fetal skeleton: sonographic findings. AJR 1995; 164: 973-9 [6]. Whitley CB, Corlin RJ. Achondrogenesis:New onsology with evidence of genetic heterogeneity. Radiology 1983; 148: 693-8