2013
DOI: 10.5958/j.2319-5886.2.2.011
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Residual nonunion in a case of two and half year old child congenital pseudoarthrosis of ipsilateral tibia and fibula treated by intramedullary fixation with kwire and allogenic cancellous strut graft: A case report

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Cited by 1 publication
(2 citation statements)
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“…2 It is found in 5,7% of patients with Neurofibromatosis type 1 (NF 1), while 40% of patients with CPT have NF 1. 3 NF 1 is an autosomal dominant disorder with incidence 1:3500 live birth. 4 Before the making of exact diagnosis for this disease, it has to exclude other conditions that clinically seen as pathological fracture in pediatric such as infection, rickets, benign or malignant tumors, and osteogenesis imperfecta.…”
Section: Introductionmentioning
confidence: 99%
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“…2 It is found in 5,7% of patients with Neurofibromatosis type 1 (NF 1), while 40% of patients with CPT have NF 1. 3 NF 1 is an autosomal dominant disorder with incidence 1:3500 live birth. 4 Before the making of exact diagnosis for this disease, it has to exclude other conditions that clinically seen as pathological fracture in pediatric such as infection, rickets, benign or malignant tumors, and osteogenesis imperfecta.…”
Section: Introductionmentioning
confidence: 99%
“…However, some cases ended in amputation. 3,6 Refracture risk increase as the younger the patient get the surgery (younger than 4-year-old), the small longitudinal plane from the healing segment, dysplastic tissue recurrence, persistent fibula pseudoarthrosis, residual ankle valgus deformity, intramedullary rod removal, and non-compliance in wearing the brace. 2 Therapy is primarily being done with surgery and it aims to gain long-lasting bony union, to prevent leg length discrepancy, to prevent mechanical axis deviation, soft tissue injury, joint stiffness, and pathological fracture.…”
Section: Introductionmentioning
confidence: 99%