1975
DOI: 10.1111/j.1748-5827.1975.tb05710.x
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Craniomandibular osteopathy in Doberman Pinschers

Abstract: Two young Doberman Pinschers with painless, firm enlargement of the mandibles were investigated. Craniomandibular osteopathy was diagnosed in each case on the basis of characteristic radiographic and gross and microscopic lesions.

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Cited by 18 publications
(32 citation statements)
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“…It is of interest to note that, although not currently reported in horses, craniomandibular osteopathy is a disease similar to HO in that it involves proliferation of long bones. This disease occurs in young dogs resulting in bilateral osseous proliferation of the mandible, tympanic bullae and less commonly other bones of the head (Watson et al . 1975, 1995; Taylor et al .…”
Section: Discussionmentioning
confidence: 99%
“…It is of interest to note that, although not currently reported in horses, craniomandibular osteopathy is a disease similar to HO in that it involves proliferation of long bones. This disease occurs in young dogs resulting in bilateral osseous proliferation of the mandible, tympanic bullae and less commonly other bones of the head (Watson et al . 1975, 1995; Taylor et al .…”
Section: Discussionmentioning
confidence: 99%
“…Although the majority of clinical reports identify bilateral involvement of the affected bones in CMO, unilateral mandibular involvement has been previously described (Watson et al 1995). The aetiopathogenesis of CMO remains poorly understood and it is likely to be multifactorial (Riser et al 1967, Watson et al 1975. In a case series of 12 Irish setters with canine leukocyte adhesion deficiency, seven developed radiographic signs consistent with CMO, supporting an underlying infectious cause for these changes (Trowald-Wigh et al 2000).…”
Section: Discussionmentioning
confidence: 99%
“…Implicated agents include viral (canine distemper virus) and bacterial infection (E. coli) (Watson et al 1995). The occurrence of CMO in a diverse range of breeds other than WHWTs also suggests that either there is an enhanced inherited susceptibility to a causative agent or there are multiple causes of the disease (Watson et al 1975, Thompson 2007.…”
Section: Discussionmentioning
confidence: 99%
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