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1.
Asian Spine Journal ; : 888-893, 2023.
Article in English | WPRIM (Western Pacific) | ID: wpr-999653

ABSTRACT

Methods@#We used 1.0-mm interval computed tomographic scan images of 100 patients (50 men and 50 women) and screw trajectory simulation software. The diameter of all screws was set at 3.5 mm, considering its common usage in real surgery. The anatomical feasibility of placing both pedicle and laminar screws on the same side was evaluated. For all feasible sides, the three-dimensional distance between the screw entry points was measured. @*Results@#In 85% of cases, both pedicle and laminar screws could be placed on both sides, allowing for the insertion of 4 screws. In 11% of cases, 2 screws could be placed on one side, while only 1 screw was feasible on the other side, resulting in the placement of 3 screws. In all 181 sides where both types of screws could be inserted, the distance between their entry points exceeded 16.1 mm, which was sufficient to prevent the collision between the screw heads. @*Conclusions@#C2 vertebra can accommodate three (11%) or four (85%) screws in 96% of cases.

2.
Br J Haematol ; 150(3): 359-64, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20497177

ABSTRACT

In order to obtain an approximate assessment of the public health burden that will be posed by the inherited disorders of haemoglobin in southern Vietnam, several thousand individuals were screened for these conditions. A smaller sample was screened for glucose-6-phosphate dehydrogenase (G6PD) deficiency. The important haemoglobin disorders identified were beta thalassaemia, haemoglobin E and a variety of different forms of alpha thalassaemia. There were sufficient G6PD-deficient individuals to materially affect malaria control programme design. The most remarkable finding was wide variation in the gene frequencies of these conditions among the ethnic groups sampled. The approximate number of babies expected to be born with clinically significant haemoglobin disorders in Vietnam was estimated from the gene-frequency data. This study emphasizes the importance of wide-scale population screening, including ethnic subgroups, to establish the requirements for inherited haemoglobin disorder programmes in resource-limited settings.


Subject(s)
Hemoglobinopathies/ethnology , Blood Specimen Collection/methods , Gene Frequency , Genotype , Glycogen Storage Disease Type I/ethnology , Glycogen Storage Disease Type I/genetics , Hemoglobin E/analysis , Hemoglobinopathies/genetics , Humans , Mass Screening/organization & administration , Mutation , Needs Assessment/organization & administration , Prevalence , Vietnam/epidemiology , alpha-Thalassemia/ethnology , alpha-Thalassemia/genetics , beta-Thalassemia/ethnology , beta-Thalassemia/genetics
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