Results 31 to 40 of about 37,693 (197)
Case Reports in Orthopedics, 2018 We present a rare case of a femoral shaft fracture in a 74-year-old woman with a preexisting untreated bilateral congenital hip dislocation and with concomitant leg length discrepancy.
Stefania Kanata, Antonios Anastasiadis
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Anesthesia for a patient with Fanconi anemia for developmental dislocation of the hip: a case report
Brazilian Journal of Anesthesiology, 2014 Fanconi anemia is a rare autosomal recessive inherited bone marrow failure syndrome with congenital and hematological abnormalities. Literature regarding the anesthetic management in these patients is limited.
Zafer Dogan +4 more
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Developmental Dynamics, EarlyView.Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki +6 more
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Easier diagnosis of congenital dislocation of the hip
South African Family Practice, 1984 No abstract available.
Solly B. Shochet
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International Journal of Gynecology &Obstetrics, EarlyView.Abstract Background Increased use of operative vaginal birth (OVB; forceps and vacuum) has been proposed as a strategy to avoid cesarean birth (CB) among individuals who elect a trial of labour after CB (TOLAC). The relative maternal safety of OVB and CB in individuals with a TOLAC is poorly understood. Objective To summarize the available evidence and
Irina I. Oltean +2 more
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Andrology, EarlyView.Abstract Background Penile sexual sensation relies on intricate neural structures that remain incompletely characterized. Immunohistological insights into their development and organization can enhance understanding of penile neuroanatomy and function, while optimizing surgical outcomes.
Alfonso Cepeda‐Emiliani +6 more
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Ultrasonography of the pediatric hip and spine [PDF]
Ultrasonography, 2017 Ultrasonography (US) is a useful screening method for the diagnosis of developmental dysplasia of the hip (DDH) and congenital spinal anomalies in infants. In addition, US is a useful, noninvasive imaging modality for the diagnosis of transient synovitis
Yeo Ryang Kang, Joonbum Koo
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Spigelian-like hernia with cryptorchidism and tibial hemimelia
Journal of Pediatric Surgery Case Reports, 2022 We describe a case of an unusual lateral congenital abdominal wall hernia. This male patient was born with a constellation of anomalies including a Spigelian-like left lower quadrant abdominal wall hernia, right tibial hemimelia, left hip dysplasia with ...
Rachel L. Bank, Eiichi Miyasaka
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Acta Obstetricia et Gynecologica Scandinavica, EarlyView.In this study of 1 126 059 pregnancies, we find evidence of comparable predictive ability for adverse perinatal outcomes across four fetal growth references, but with notable differences in sensitivity and false positive rate (FPR). The WHO reference demonstrated balanced performance in detecting at‐risk fetuses, suggesting its suitability for clinical
Linda Lindström +6 more
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Defining the limbus in developmental dysplasia of the hip – Less is more: A Case Report
Journal of Orthopaedic Reports, 2023 Background: Developmental dysplasia of the hip (DDH) includes a spectrum of congenital and/or developmental hip abnormalities that are caused by a shallow acetabulum, which can lead to hip subluxation or dislocation.
Varun Muddaluru +2 more
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