Browsing by Author "Filippi Nussbaum, Jorge Luis"
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- ItemA New Classification System for Pilon Fractures Based on CT Scan : An Independent Interobserver and Intraobserver Agreement Evaluation(2020) Palma Munita, Joaquín Hernán; Villa Massiff, Andrés Alberto; Mery Ponce, Pablo Agustín; Abarca Montano, Mario; Mora, A.; Pena, A.; Urrutia Escobar, Julio Octavio; Filippi Nussbaum, Jorge Luis
- ItemArthroscopic treatment of pigmented villonodular synovitis of the ankle : a clinical case report and review(2019) Salas González, Soledad; Urrutia Jarpa, Tomás; Filippi Nussbaum, Jorge Luis
- ItemBone block lengthening of the proximal interphalangeal joint for managing the floppy toe deformity(2010) Myerson, Mark S.; Filippi Nussbaum, Jorge Luis
- ItemComplications after Metatarsal Osteotomies for Hallux Valgus : Malunion, Nonunion, Avascular Necrosis, and Metatarsophalangeal Osteoarthritis(2020) Filippi Nussbaum, Jorge Luis; Briceño Ferrada, Jorge Andrés
- ItemSíndrome del túnel del tarso posterior bilateral por músculo flexor digitorum longus accesorio; reporte de un caso y descripción de técnica quirúrgica Bilateral posterior(2015) Schmidt-Hebbel, A.; Elgueta, J.; Villa, A.; Mery Ponce, Pablo Agustín; Filippi Nussbaum, Jorge Luis
- ItemXantomatosis cerebrotendínea: Una causa de aumento de volumen bilateral del tendón de Aquiles. Caso clínico(2009) Filippi Nussbaum, Jorge Luis; Irarrázaval, Sebastián; Preredo O., Pilar; Mellado T., PatricioCerebrotendinous xanthomatosis is an inherited autosomal recessive disease caused by a mutation in the gene for the sterol 27-hydroxylase enzyme, which determines the accumulation of plasmatic cholestanol in various tissues. The natural history of this disease is characterized by chronic diarrhea beginning in childhood, cataract in youth, tendinous xanthomas in adulthood and later progressive neurological dysfunction manifested as dementia, psychiatric disorders, cerebellar, pyramidal or extrapyramidal signs or seizures. We report a 39 year-old male with a history of diarrhea during childhood and bilateral cataracts requiring surgery at 20 years of age, who evolves later with psychiatric disorders and bilateral increased volume in Achilles tendons. High levels of plasmatic cholestanol and magnetic resonance imaging confirmed the diagnosis of this disease.