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A Newborn with Multiple Fractures in Osteogenesis Imperfecta: A Case Report

INTRODUCTION: Multiple bone fractures in a newborn can be associated with osteogenesis imperfect (OI). OI is a rare genetic disorder that causes Type I collagen synthesis disturbance results in bone fragility. CASE REPORT: We present a female newborn which had numerous fractures of the humerus, bila...

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Autores principales: Bayram, Serkan, Mert, Lezgin, Anarat, Fikret Berkan, Chodza, Mechmed, Ergin, Ömer Naci
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298723/
https://www.ncbi.nlm.nih.gov/pubmed/30584522
http://dx.doi.org/10.13107/jocr.2250-0685.1116
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author Bayram, Serkan
Mert, Lezgin
Anarat, Fikret Berkan
Chodza, Mechmed
Ergin, Ömer Naci
author_facet Bayram, Serkan
Mert, Lezgin
Anarat, Fikret Berkan
Chodza, Mechmed
Ergin, Ömer Naci
author_sort Bayram, Serkan
collection PubMed
description INTRODUCTION: Multiple bone fractures in a newborn can be associated with osteogenesis imperfect (OI). OI is a rare genetic disorder that causes Type I collagen synthesis disturbance results in bone fragility. CASE REPORT: We present a female newborn which had numerous fractures of the humerus, bilateral clavicle, and bilateral femur. Her delivery was at 36 weeks gestation by spontaneous vaginal delivery. She had has not any pathological symptom at 2 weeks after birth, the patient had a fracture of the humerus, bilateral clavicle, and femur without any trauma. Genetic analysis of the patient was reported and OI diagnosed. The patient was followed up for 8 months with regularly and without any complication. CONCLUSION: Multiple fractures with OI in an infant after birth may require an accurate orthopedic plan for diagnosing and treatment.
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spelling pubmed-62987232018-12-24 A Newborn with Multiple Fractures in Osteogenesis Imperfecta: A Case Report Bayram, Serkan Mert, Lezgin Anarat, Fikret Berkan Chodza, Mechmed Ergin, Ömer Naci J Orthop Case Rep Case Report INTRODUCTION: Multiple bone fractures in a newborn can be associated with osteogenesis imperfect (OI). OI is a rare genetic disorder that causes Type I collagen synthesis disturbance results in bone fragility. CASE REPORT: We present a female newborn which had numerous fractures of the humerus, bilateral clavicle, and bilateral femur. Her delivery was at 36 weeks gestation by spontaneous vaginal delivery. She had has not any pathological symptom at 2 weeks after birth, the patient had a fracture of the humerus, bilateral clavicle, and femur without any trauma. Genetic analysis of the patient was reported and OI diagnosed. The patient was followed up for 8 months with regularly and without any complication. CONCLUSION: Multiple fractures with OI in an infant after birth may require an accurate orthopedic plan for diagnosing and treatment. Indian Orthopaedic Research Group 2018 /pmc/articles/PMC6298723/ /pubmed/30584522 http://dx.doi.org/10.13107/jocr.2250-0685.1116 Text en Copyright: © Indian Orthopaedic Research Group http://creativecommons.org/licenses/by-nc/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Bayram, Serkan
Mert, Lezgin
Anarat, Fikret Berkan
Chodza, Mechmed
Ergin, Ömer Naci
A Newborn with Multiple Fractures in Osteogenesis Imperfecta: A Case Report
title A Newborn with Multiple Fractures in Osteogenesis Imperfecta: A Case Report
title_full A Newborn with Multiple Fractures in Osteogenesis Imperfecta: A Case Report
title_fullStr A Newborn with Multiple Fractures in Osteogenesis Imperfecta: A Case Report
title_full_unstemmed A Newborn with Multiple Fractures in Osteogenesis Imperfecta: A Case Report
title_short A Newborn with Multiple Fractures in Osteogenesis Imperfecta: A Case Report
title_sort newborn with multiple fractures in osteogenesis imperfecta: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298723/
https://www.ncbi.nlm.nih.gov/pubmed/30584522
http://dx.doi.org/10.13107/jocr.2250-0685.1116
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