Relevant bibliographies by topics / Congenitalshort Femur Fracture Infant Case Report

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Academic literature on the topic 'Congenitalshort Femur Fracture Infant Case Report'

Author: Grafiati
Published: 5 June 2025
Last updated: 15 July 2025

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Journal articles on the topic "Congenitalshort Femur Fracture Infant Case Report"

1

Amine Oukhouya, Mohamed, Hicham Abdellaoui, Mohammed Tazi, Karima Atarraf, and Moulay Abderrahmane Afifi. "FRACTURE ONCONGENITAL SHORT FEMUR: A CASE REPORT." International Journal of Advanced Research 10, no. 07 (2022): 427–30. http://dx.doi.org/10.21474/ijar01/15051.

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Background:Congenital short femur is characterized by a global femoral hypoplasia, classified in 5 types, type1 is a simple hypoplasia, revealed in our patient in the context of a fracture. Clinical case:The article presents a clinical observation of a one month old male infant who admitted on account of trauma of the leftlowerlimb,an x-ray revealed a fracture on congenital short femur type 1. Discussion: Short congenital femur is the most common growth deficiency of the femur, with five types: type 1: simple hypoplasia of the femur type 2: short femur with angulation type 3: short femur with
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2

Melo, Áurea Nogueira de, Lívia Lucena de Medeiros, Rogério Maciel Nobre, Manuel Moreira Neto, and Antônio Sérgio Macedo Fonseca. "Non-traumatic fracture of the femur in a infant with recurrent epileptic seizures: case report." Journal of Epilepsy and Clinical Neurophysiology 16, no. 2 (2010): 77–79. http://dx.doi.org/10.1590/s1676-26492010000200007.

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OBJECTIVE: To report a rare non traumatic fracture of femur after a partial secondarily generalized tonic seizure in a infant. DESCRIPTION: A 7-month-old female patient was referred to the Pediatric Hospital with two complaints: 1) frequent epileptic seizures since the age of 3 months and 2) intermittent crying when the left leg is moved or manipulated after last seizures. Computerized tomography of the hipbone revealed left spontaneous transepiphyseal fracture of the femur (Delbet type 1). Clinical, metabolic and radiological investigation did not reveal osteopenia or rickets. A family study
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3

Bombah, Freddy Mertens, Alphonse Ngalame, René Essomba, Yannick Ekani Boukar, Enrique Zoa Nkoa, and Daniel Handy Eone. "Obstetric fracture of the femur during cesarean section in a preterm baby: A case report." Journal of Orthopedics and Orthopedic Surgery 2, no. 3 (2021): 22–24. http://dx.doi.org/10.29245/2767-5130/2021/3.1150.

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Introduction: Obstetric fractures or Birth fractures are rare events following childbirth. Although fracture of the femur is a relatively uncommon injury, it is the most common fracture of the lower extremity in the newborn. Since evolution of cesarean section rates in Africa, it is one of the most commonly practiced modes of delivery for breech. We described one case of fracture of the femur at cesarean section treated at Adlucem hospital in bonabéri-Douala (Cameroon). Case report: A 2.1 kg male infant was delivered by lower segment cesarean section for breech presentation. Clinical and radio
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4

Tiwary, Rimple, and Manish Kumar Tiwary. "Caesarean section with breech presentation and shaft femur fracture in newborn: a rare case report." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 12, no. 1 (2022): 246. http://dx.doi.org/10.18203/2320-1770.ijrcog20223503.

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Vaginal delivery for breech presentation is always associated with a higher risk of injury to the newborn as compared to caesarean delivery. A male infant was delivered by elective caesarean section at 40 weeks of gestation for breech presentation. During extraction, the newborn sustained a right femur shaft fracture. A simple splint with immobilization along with leg raise led to complete healing without complication. Caesarean delivery is associated with a reduced risk of newborn birth injuries as compared to vaginal and instrumental delivery but rare accidental complication can be possible.
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5

R, Nithiya Kumar, Sze Lyn Jeanne W, Janet Yeow Hua H, et al. "CASE REPORT: PAMIDRONATE INFUSION IN A 3-MONTH OLD INFANT WITH OSTEOGENESIS IMPERFECTA." Journal of the ASEAN Federation of Endocrine Societies 34 (July 17, 2019): 65. https://doi.org/10.15605/jafes.034.s115.

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INTRODUCTIONBisphosphate is a well-recognised treatment for children with osteogenesis imperfecta (OI). However, for neonatalonset or young infants, there are no large groups reported and no clear guideline on the safest dosing regimen. CASEOur patient presented with a left femur fracture at the age of 1.5 months. A week later, she was diagnosed with severe OI when she suffered four more fractures despite minimal handling; bilateral humerus, left clavicle and right femur. Her sclerae had a tinge of blue at first review. She was started on pamidronate two-monthly cycle (regimen as below) at 3 m
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6

Phancharone, S. "Fracture femur: a clinical sign of child abuse,a case report in a 3 month old infant." Chulalongkorn Medical Journal 44, no. 9 (2000): 703–9. http://dx.doi.org/10.58837/chula.cmj.44.9.7.

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7

Bezirganoglu, Handan, and Kubra Adanur Saglam. "An Unusual Case of Neonatal Hypotonia and Femur Fracture: Neuromuscular Variant of Glycogen Storage Disease Type IV." Children 10, no. 8 (2023): 1375. http://dx.doi.org/10.3390/children10081375.

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Glycogen storage disease type IV (GSD IV) (OMIM #232500) is an autosomal recessive disorder caused by deficiency of the glycogen-branching enzyme. Here, we report a patient presenting with prematurity and severe hypotonia resulting from a complicated pregnancy with polyhydramnios. During her stay in the neonatal unit, the infant remained dependent on a ventilator, and her movements were mostly absent, except for occasional small movements of her fingers. A spontaneous fracture of femur shaft occurred in the postnatal fourth week. Whole-exome sequencing of DNA from the patient revealed a homozy
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8

Mohamed, Amine Oukhouya Hicham Abdellaoui, and Tazi Karima Atarraf and Moulay Abderrahmane Afifi Mohammed. "FRACTURE ONCONGENITAL SHORT FEMUR: A CASE REPORT." July 13, 2022. https://doi.org/10.5281/zenodo.6984767.

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<strong>Background:</strong>Congenital short femur is characterized by a global femoral hypoplasia, classified in 5 types, type1 is a simple hypoplasia, revealed in our patient in the context of a fracture. <strong>Clinical case:</strong>The article presents a clinical observation of a one month old male infant who admitted on account of trauma of the leftlowerlimb,an x-ray revealed a fracture on congenital short femur type 1. <strong>Discussion</strong>: Short congenital femur is the most common growth deficiency of the femur, with five types: type 1: simple hypoplasia of the femur type 2: sh
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9

Jafari Kafiabadi, Meisam, Mehrdad Sadighi, Amir Sabaghzadeh, Farsad Biglari, Saber Barazandeh Rad, and Adel Ebrahimpour. "Bilateral Floating Knee Injuries in an Infant: A Case Report and Literature Review." Journal of Orthopedic and Spine Trauma, December 24, 2021. http://dx.doi.org/10.18502/jost.v7i3.8112.

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Background: Floating knee injury is defined as ipsilateral fractures of the femur and tibia. It was mostly seen among young men and is generally caused by high-velocity trauma such as motor vehicle accidents and falling from height. Although isolated fractures of the femur or tibia are relatively common in children, floating knee injuries are rare in adolescents and even less frequent in younger children.&#x0D; Case Report: In this study, we reported a case of bilateral floating knee injuries of a 10-month old girl infant. Radiographic examinations revealed diaphyseal fracture of the left femu
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10

Moscoso, Joana, Mariana Dias, Rita Barreira, and Duarte Malveiro. "Unexplained fractures in an infant, a clue to osteogenesis imperfecta." International Journal of Medical Reviews and Case Reports, 2023, 1. http://dx.doi.org/10.5455/ijmrcr.172-1683126275.

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Introduction: Osteogenesis imperfecta (OI) is an autosomal dominant disorder that affects about 6-7/100,000 patients. Case report: We describe a term neonate, with a supervised pregnancy and fetal ultrasonography at 23 weeks with bone dysplasia suspicion. Physical exam revealed axial hypotonia, increased anterior fontanel with distant cranial sutures and small and tapered nose. Skeletal radiography showed hypomineralization and wormian bones of cranial calotte, thin ribs and short and curved femurs. Genetic test revealed heterozygous variant of p.(Gly328Ser) in exon 19 of the COL1A2 gene, of t
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