scholarly journals Early Diagnosis and Prevention of Repetitive Strain Injury Induced Carpal Tunnel Syndrome among Computer Users

2018 ◽  
Vol 04 (01) ◽  
Author(s):  
Sonia Agrawal ◽  
Rajajeyakumar M
Neurology ◽  
2001 ◽  
Vol 56 (11) ◽  
pp. 1568-1570 ◽  
Author(s):  
J. Clarke Stevens ◽  
J. C. Witt ◽  
B. E. Smith ◽  
A. L. Weaver

Author(s):  
Domingo Ly-Pen ◽  
José-Luis Andreu ◽  
Gema de Blas ◽  
Alberto Sánchez-Olaso ◽  
Jesús Jiménez San Emeterio

Introduction: Mucopolysaccharidosis type I (MPS-I: Hurler/Scheie´s disease) is a rare disease with a wide spectrum of severity. This results in underdiagnosis and delayed diagnosis. Prognosis greatly depends upon early diagnosis. The availability of reliable diagnostic tests and the existence of enzyme replacement therapy and/or hematopoietic stem cell transplantation, make an early diagnosis of these patients extremely important. Carpal tunnel syndrome (CTS) is among one of the most common findings in MPS I, whilst CTS is very uncommon in infancy and young adulthood. Objective: To ascertain the prevalence of MPS-I among children and young adults (≤ 30 years) diagnosed with CTS in our population. To get an early diagnosis of MPS-I patients. Material and Methods: This is a cross-sectional prospective study of a cohort of patients with an electromyogram-confirmed diagnosis of CTS. Our total population is over 600,000 people of an urban area of Madrid. We searched for children and young adults with suggestive symptoms of CTS. χ2 for categorical variables and Student “t” analysis or Anova test for quantitative variables were used. Results: 12 patients were included, 10 females, range 8-28 years, mean 23, median 23.5. Two patients had a low α-L-Iduronidase activity. Nonetheless, the results of confirmatory test of enzymatic activity of α-L-Iduronidase in lymphocytes were negative in both cases. Conclusions: We did not find any MPS-I in our series of CTS in children and young adults. Larger series will be needed to ascertain if this approach is valid for early diagnosis of MPS-I in the paediatric population.


2020 ◽  
Vol 22 (3) ◽  
pp. 507-515 ◽  
Author(s):  
Agnese Milandri ◽  
Andrea Farioli ◽  
Christian Gagliardi ◽  
Simone Longhi ◽  
Fabrizio Salvi ◽  
...  

2019 ◽  
Vol 9 (4) ◽  
pp. 309-313 ◽  
Author(s):  
Chafic Karam ◽  
Diana Dimitrova ◽  
Megan Christ ◽  
Stephen B. Heitner

BackgroundHereditary transthyretin amyloidosis (hATTR) is associated with significant morbidity and mortality. Early diagnosis and treatment are essential to improve patient's outcome. Carpal tunnel syndrome (CTS) is a common complication of hATTR amyloidosis. However, because CTS is also common in the general population, we wanted to assess whether CTS, when associated with systemic manifestations, could help direct physicians to screen for TTR gene mutation and early diagnosis.MethodsWe reviewed the charts and interviewed the patients with hATTR seen between 2017 and 2018. We noted the details of CTS diagnosis, treatment, and other systemic features of the disease.ResultsSeventeen of the 23 patients studied had CTS. CTS was the first manifestation of the disease in 10 of 17 patients. On average, CTS symptoms occurred 10.4 years before their diagnosis of hATTR amyloidosis. In 6 of 10 patients with CTS, the following systemic symptoms were present as the first manifestation: erectile dysfunction, dysautonomia, polyneuropathy, exercise intolerance, and gastrointestinal and ocular symptoms.ConclusionCTS occurs in most patients with hATTR amyloidosis and frequently precedes the hATTR diagnosis. Most patients with CTS preceding hATTR diagnosis have systemic features. Recognizing systemic features at the time of CTS presentation may help in early diagnosis of hATTR amyloidosis.


2001 ◽  
Vol 2001 (2) ◽  
pp. 2-10 ◽  
Author(s):  
Khema R. Sharma ◽  
Francisco Rotta ◽  
Jose Romano ◽  
D. Ram Ayyar

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