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The Bone & Joint Journal
Vol. 100-B, Issue 6 | Pages 828 - 828
1 Jun 2018
Jones DHA


The Bone & Joint Journal
Vol. 96-B, Issue 3 | Pages 420 - 425
1 Mar 2014
Fahal AH Shaheen S Jones DHA

This article presents an overview of mycetoma and offers guidelines for orthopaedic surgeons who may be involved in the care of patients with this condition.

Cite this article: Bone Joint J 2014;96-B:420–5.


The Journal of Bone & Joint Surgery British Volume
Vol. 92-B, Issue 9 | Pages 1312 - 1315
1 Sep 2010
Jones DHA


The Journal of Bone & Joint Surgery British Volume
Vol. 88-B, Issue 2 | Pages 276 - 276
1 Feb 2006
JONES DHA


The Journal of Bone & Joint Surgery British Volume
Vol. 87-B, Issue 10 | Pages 1406 - 1410
1 Oct 2005
Ramachandran M Lau K Jones DHA

In five children, six forearms with a fixed pronation deformity secondary to congenital radioulnar synostosis were treated by a derotation osteotomy of the distal radius and the midshaft of the ulna.

There were three boys and two girls with a mean age of 4.9 years (3.5 to 8.25) who were followed up for a mean of 29 months (18 to 43). The position of the forearm was improved from a mean pronation deformity of 68° (40° to 80°) to a pre-planned position of 10° of supination in all cases. Bony union was achieved by 6.3 weeks with no loss of correction. There was one major complication involving a distal radial osteotomy which required exploration for a possible compartment syndrome.


The Journal of Bone & Joint Surgery British Volume
Vol. 87-B, Issue 9 | Pages 1169 - 1170
1 Sep 2005
Jones DHA


The Journal of Bone & Joint Surgery British Volume
Vol. 82-B, Issue 7 | Pages 1083 - 1083
1 Sep 2000
JONES DHA


The Journal of Bone & Joint Surgery British Volume
Vol. 80-B, Issue 1 | Pages 184 - 184
1 Jan 1998
Jones DHA


The Journal of Bone & Joint Surgery British Volume
Vol. 79-B, Issue 4 | Pages 576 - 582
1 Jul 1997
Haddad FS Jones DHA Vellodi A Kane N Pitt MC

Children with a mucopolysaccharidosis or mucolipidosis suffer progressive disability of the hands, particularly in relation to dysfunction of the median nerve. This is an increasing problem because bone-marrow transplantation has dramatically improved survival without apparently changing the musculoskeletal manifestations. We have reviewed 48 children with these syndromes who required carpal tunnel decompression, recording symptoms, signs, radiological, electrophysiological and operative findings, histology and upper-limb function. In these children the carpal tunnel syndrome differs from that seen in adults. Symptoms are rare but signs such as decreased sweating, pulp atrophy, thenar wasting and manual clumsiness are much more common. At operation, the flexor retinaculum was thickened and a mass of white tenosynovium engulfed the flexor tendons. Most patients had some definite nerve constriction with a thickened epineurium.

Functional improvement was seen after early decompression, with some benefit from simultaneous tendon release. Regular physiotherapy helped to maintain increased hand movement.

We describe our assessment protocol, the physiotherapy and operative regime and the standard functional review which helps to maximise function in the hands and upper limbs of these children.