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A thorough analysis of data on the correlation between COL9A1 polymorphisms and the susceptibility to congenital talipes equinovarus: a meta-analysis
BackgroundCongenital talipes equinovarus (CTEV) is a prevalent pediatric deformity with a multifactorial etiology. The objective of this...
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Functional, clinical, and radiological outcomes of split anterior tibial tendon transfers in patients with sequelae of congenital talipes equinovarus
ObjectiveThis retrospective analysis aimed to assess the effectiveness of Split Tibialis Anterior Tendon Transfer (Split TATT) in treating residual...
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Novel report on congenital talipes equinovarus (CTEV) following olanzapine exposure during pregnancy: case report and short review
Olanzapine is widely used during pregnancy to manage mood and psychotic disorders with overall beneficial effects. There have been past reports of...
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Promising results in a 3-year follow-up for adults undergoing a one-stage surgery for residual talipes equinovarus as part of a humanitarian mission in Vietnam
BackgroundRigid talipes equinovarus (TEV) is a complex foot deformity in which the foot is fixed in a plantarflexed, inverted, and adducted position....
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Correlation of radiographic parameters with clinical correction in idiopathic congenital talipes equinovarus undergoing Ponseti treatment
PurposeIdiopathic congenital talipes equinovarus is the most commonly encountered congenital deformity of the foot. Ponseti technique of manipulation...
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Novel PIP5K1C variant identified in a Chinese pedigree with lethal congenital contractural syndrome 3
BackgroundBiallelic pathogenic variants in PIP5K1C (MIM #606,102) lead to lethal congenital contractural syndrome 3 (LCCS3, MIM #611,369), a rare...
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Calcaneocuboid capsuloligamentous soft-tissue entrapment: a rare cause of acquired equinovarus deformity
Acquired equinovarus deformity is rare, with most cases related to congenital disorders such as clubfoot. We describe a unique case of traumatic...
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Congenital Spinal Canal Stenosis (CSS): A Case Report of Two Similar Rare Anomalies
Congenital spinal canal stenosis is a very rare vertebral disorder. The etiology is not clearly defined. Genetic, nutritional, and environmental...
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Trends in congenital clubfoot prevalence and co-occurring anomalies during 1994–2021 in Denmark: a nationwide register-based study
BackgroundCongenital talipes equinovarus (clubfoot) is a common musculoskeletal anomaly, with a suspected multifactorial etiopathogenesis. Herein, we...
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Evaluation of genetic susceptibility of common variants in SOX9 in patients with congenital talipes equinovarus in the Han Chinese population
BackgroundCongenital talipes equinovarus (CTEV) is a common birth defect that causes severe deformities of one or both feet. Genetics have been...
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Incidence and prevalence of congenital clubfoot in Apulia: a regional model for future prospective national studies
BackgroundCongenital clubfoot is a fairly common and severe congenital malformation, most often of idiopathic origin. A smaller percentage of cases...
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Clinicopathological profile and management challenges of congenital encephaloceles in a tertiary hospital in southwest Nigeria
PurposeA congenital encephalocele is the herniation of intracranial contents through skull defects of various sizes. Depending on the site, content,...
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Post-discharge follow-up of congenital duodenal obstruction patients: a systematic review
PurposeLong-term follow-up of congenital duodenal obstruction patients often falls on care providers with little experience of this condition. We...
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Trisomy 5p with bilateral congenital diaphragmatic hernia: a case report
BackgroundBilateral congenital diaphragmatic hernia (CDH) is very rare. A few studies have reported the pathogenic role of 5p in CDH.
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A 5-years results of the Ponseti method in the treatment of congenital clubfoot: a retrospective study
BackgroundClubfoot is a common congenital deformity affecting mobility of children. It leads to pain and disability. The Ponseti treatment method is...
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Terminal microdeletion of chromosome 18 in a Malaysian boy characterized with few features of typical 18q- deletion syndrome: a case report
BackgroundThe 18q- deletion syndrome is a rare congenital chromosomal disorder caused by a partial deletion of the long arm of chromosome 18. The...
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Arthrogryposis multiplex congenita in a child with congenital fractures: a case report
BackgroundBruck syndrome is an exceedingly rare form of osteogenesis imperfecta, inherited autosomal recessively and presenting with the concurrence...
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Two-dimensional and four-dimensional ultrasound in the diagnosis of non-cardiac fetal congenital anomalies in high risk pregnancies: a comparative study
BackgroundThe high incidence of non-cardiac congenital anomalies in high-risk pregnancies is a major worldwide health problem. Congenital deformities...
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The diagnostic dilemma of congenital foot deformity in pediatrics: could adding ultrasound be problem solving?
BackgroundFoot deformity is one of the most common congenital musculoskeletal anomalies in the pediatric age group. Accurate diagnosis can be...
