Cesarean section newborn with multiple fractures: an Osteogenesis Imperfecta case report

Publish Year: 1392
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:

JR_INTJMI-3-3_005

تاریخ نمایه سازی: 15 مهر 1398

Abstract:

Osteogenesis Imperfecta (OI) or Brittle bone disease, is a rare genetic disorder that causes type Icollagen synthesis disturbance results in bone fragility.We present a female newborn which had numerous fractures in the arm and femur. Her delivery was at38 weeks gestation by caesarean section. Prenatal ultrasound revealed bone swelling and long bonesshortness. The patient is pale blue sclera. 36 days after birth, the patient had a fracture in her left femur.Genetic analysis of the patient was reported. Protests by clinical, ultrasound and x-ray taken duringpregnancy for this patient reported Osteogenesis Imperfecta type V.shortening, swelling and deformity of the long bones during prenatal sonography can prove OsteogenesisImperfecta before birth and select the correct orthopedic plan for treatment.

Authors

Mohammad Hossein Kariminasab

MD, Assistance professor Department of Orthopedic Surgery, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran

Masoud Shayeste-Azar

MD, Assosiated professor, Department of Orthopedic Surgery, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran

Mohamad Hossein Kariminasab

MD, Assosiated professor, Department of Orthopedic Surgery, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran

Majid Sajjadi Saravi

MD, Assistance professor Department of Orthopedic Surgery, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran