2009
DOI: 10.1016/j.ejpn.2008.04.006
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Congenital thenar hypoplasia with absent radial artery – A case report

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Cited by 5 publications
(4 citation statements)
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“…Incidence of bone -muscle anomalies of the hand and forearm is within the range of 1/30.000 and 1/100.000 9. Whilst male-female ratio is 3:2, thenar muscle anomalies and thumb hypoplasias can be seen in isolation, as in Cavanagh’s syndrome and are commonly seen with syndromes such as Holt-Oram, TAR, Fanconi, VACTERL and radial bone anomalies 2,10–13. Cavanagh’s syndrome is a rare anomaly of the upper extremities that presents with unilateral or bilateral hypoplasia of the thenar eminence 2.…”
Section: Discussionmentioning
confidence: 99%
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“…Incidence of bone -muscle anomalies of the hand and forearm is within the range of 1/30.000 and 1/100.000 9. Whilst male-female ratio is 3:2, thenar muscle anomalies and thumb hypoplasias can be seen in isolation, as in Cavanagh’s syndrome and are commonly seen with syndromes such as Holt-Oram, TAR, Fanconi, VACTERL and radial bone anomalies 2,10–13. Cavanagh’s syndrome is a rare anomaly of the upper extremities that presents with unilateral or bilateral hypoplasia of the thenar eminence 2.…”
Section: Discussionmentioning
confidence: 99%
“…9 Whilst male-female ratio is 3:2, thenar muscle anomalies and thumb hypoplasias can be seen in isolation, as in Cavanagh's syndrome and are commonly seen with syndromes such as Holt-Oram, TAR, Fanconi, VACTERL and radial bone anomalies. 2,[10][11][12][13] Cavanagh's syndrome is a rare anomaly of the upper extremities that presents with unilateral or bilateral hypoplasia of the thenar eminence. 2 Typical clinical, radiographic, and electrophysiologic findings confirm the diagnosis.…”
Section: Discussionmentioning
confidence: 99%
“…CTH can be an isolated defect as in Cavanagh syndrome ( Cavanagh et al, 1979 ) or may be accompanied by cardiac abnormalities ( Holt and Oram, 1960 ) or ocular abnormalities ( Okihiro et al, 1977 ). Absence of radial artery has also been reported in association with CTH ( Fernandez et al, 2009 ). CTH may be unilateral or bilateral.…”
Section: Introductionmentioning
confidence: 90%
“…Most commonly, this is associated with abnormal median sensory nerve studies and subsequently diagnosed as CTS. However, when median sensory potentials are normal and there is no clinical or electrophysiologic evidence of neurogenic thoracic outlet syndrome, cervical radiculopathy, distal myopathy, motor neuron disease or Lambert-Eaton Myaesthenic Syndrome, the electromyographer must consider anomalous innervations and congenital anomalies [8].…”
Section: Introductionmentioning
confidence: 99%