2005
DOI: 10.1111/j.1085-9489.2005.10312.x
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Carpal tunnel syndrome or congenital hand anomaly: a clinical and electromyographic study

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Cited by 3 publications
(3 citation statements)
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“…1,10 Other published and possible conditions that might provoke carpal tunnel syndrome in children are listed in Table 3. 2,914 In carpal tunnel syndrome secondary to mucopolysaccharidoses and mucolipidoses, clinical signs typical of adult carpal tunnel syndrome are rarely seen, and difficulty with fine motor tasks is the most frequent finding (as in our case 6). In such cases, carpal tunnel syndrome probably develops because of a combination of factors, such as excessive lysosomal storage in the connective tissue of the flexor retinaculum and anatomic changes caused by bone dysplasia.…”
Section: Discussionmentioning
confidence: 61%
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“…1,10 Other published and possible conditions that might provoke carpal tunnel syndrome in children are listed in Table 3. 2,914 In carpal tunnel syndrome secondary to mucopolysaccharidoses and mucolipidoses, clinical signs typical of adult carpal tunnel syndrome are rarely seen, and difficulty with fine motor tasks is the most frequent finding (as in our case 6). In such cases, carpal tunnel syndrome probably develops because of a combination of factors, such as excessive lysosomal storage in the connective tissue of the flexor retinaculum and anatomic changes caused by bone dysplasia.…”
Section: Discussionmentioning
confidence: 61%
“…In most cases, childhood carpal tunnel syndrome is a secondary phenomenon. [9][10][11][12] The first signs of carpal tunnel syndrome in children can be overlooked. Hand clumsiness in 4 of our 11 patients had not been attributed to carpal tunnel syndrome for a long time.…”
Section: Discussionmentioning
confidence: 99%
“…In pediatric patients, median nerve (MN) mononeuropathy is rarely documented. [1][2][3][4][5][6][7][8][9][10][11][12][13][14] In this population, TMA has more often been attributed to malformations of the radial carpal bones (►Table 1), the most frequent of which is a regional defect known as Cavanagh syndrome. 3 Structural malformations cause the atrophy through different mechanisms, among which are disuse arising from low joint motility, anomalous muscle insertion, and muscle agenesis and/or hypoplasia.…”
Section: Introductionmentioning
confidence: 99%