Results 41 to 50 of about 12,225 (269)
Oral maxillary exostosis [PDF]
Key Clinical MessageOral maxillary exostoses are proliferating bone lesions with an unknown etiology occurring on the cortical plates both in the maxilla and in the mandible of young individuals, showing a typical slow but continuous enlargement. No treatment is usually required unless they create esthetic or functional limitations during follow‐up ...
Luisa Limongelli +4 more
openaire +3 more sources
Differential diagnosis of nail apparatus lesions in subungual exostosis
Background. Subungual exostosis is an overgrowth of bone and/or cartilage tissue in the area of the distal phalanx of the finger. The etiopathogenesis of the disease remains incompletely understood.
R. V. Saranyuk +2 more
doaj +1 more source
Observation of experimental lathyrism in the rat [PDF]
The clinical manifestations, roentgenologic studies, and histopathologic findings of the central nervous system of rats with induced lathyrism were described.
Lee, HUN Jae
core +1 more source
Exostosis in the Hand: Case Series and Literature Review
Introduction: This study reviews the exostosis in hand in our locality and compares those in the literature. Methods: A retrospective study was conducted by reviewing the cases collected from 2000 to 2010.
Sze-Yan Chan +3 more
doaj +1 more source
A 62-year-old heavy smoker woman presented to the outpatient otorhinolaryngology clinic with a two week history of dysphagia. On routine examination, an incidental finding of a 2.5 cm hard mass that seems to be liberated in the midline of the hard ...
Omar M. Bargas
doaj +1 more source
El síndrome de fricción escapulotorácica, resalto o chasquido escapular es un cuadro poco frecuente, descrito, por primera vez, por Boinet, en 1867. Se produce por una incongruencia en la articulación escapulotorácica, asociada a múltiples causas, como ...
Juan Andrés Pinzón Escobar +2 more
doaj +1 more source
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
wiley +1 more source
Distal tibial interosseous osteochondroma with impending fracture of fibula – a case report and review of literature [PDF]
Osteochondromas arising from the interosseous border of the distal tibia and involving distal fibula are uncommon. We present a 16 year old young boy with an impending fracture, erosion and weakness of the distal fibula, secondary to an osteochondroma ...
Abdul Q Salaria +5 more
core +2 more sources
Clinical and Genetic Significance of Chromosomal Microarray Screening of Asymptomatic Newborns
Among 99 asymptomatic newborns with abnormal low‐resolution chromosomal microarray (LR‐CMA) screening, 70.7% harbored microduplication/microdeletions with syndromic implications. However, only a minority exhibited developmental concerns during early follow‐up, highlighting the need for cautious interpretation.
Naye Choi, Hwa Young Kim, Jung Min Ko
wiley +1 more source
Purpose: The objective of this study was to determine the prevalence of exostosis in the Mississippi population. Methods: The patient archives of the UMMC School of Dentistry between January 2018 and May 2021 were examined.
Landon Wilson +5 more
doaj +1 more source

