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Allogeneic bone in the treatment of tumors, trauma, and congenital anomalies of the hand.

Because autogenous bone grafts are histocompatible by definition and because the hand does not require massive bone grafts, one may question the indications for using allogeneic bone in the hand. Although humans have been shown to develop donorgraft specific antibodies following large osteochondral allografts, these antibodies have not yet been noted after smaller bone grafts nor is the clinical significance of these antibodies clear. The use of allogeneic bone better satisfies the architectural and strength requirements for reconstruction when there is a need for osteochondral grafts, strong cortical grafts to allow secure fixation and early motion, and small tubular grafts that meet the demands of minimizing bulk in the hand. For the repair of osteochondral defects, autogenous grafts (ie, fibular head or metatarsal head) impose donor site deficits that can be clinically significant. In addition, grafts such as the fibular head do not provide reconstruction of a congruent joint surface. Strong cortical bone is an asset in metacarpal reconstruction; it enhances the quality of internal fixation, which in turn allows hand therapy to be started early, an essential treatment following hand injuries. A stiff hand after reconstruction will result despite excellent bony reconstruction if the fixation does not allow early motion. Autogenous cortical grafts donor sites (eg, ulna or tibia) can cause donor site morbidity, including fracture of weakened bone. The need for small tubular grafts is especially important in pediatric patients. Strong autogenous corticocancellous grafts are difficult to obtain in children, and these grafts are bulky and difficult to insert. In addition, for adults and children, the lack of a donor site means a much shorter hospital stay.

Adult↗

[Coffin-Lowry syndrome. Description of 2 cases associated with cardiovascular anomalies].

In this work the authors describe two cases of Coffin-Lowry syndrome, diagnosed in two brothers of different age and with a different degree of evolution of the illness. The brothers present the mitral prolapse association. The clinic and instrumental examination have been executed. The various pathogenetic hypothesis have been discussed and the authors propose the most recent that considers the fibroblast incapable to produce the substances of connective matrix. This hypothesis explain also the evolution and the progression of the lesion at the interested organs (skin, joints, bones, heart). The illness is genetic, with a X-linked, semidominant transmission.

Abnormalities, Multiple↗

Free flap coverage of the hand.

The microvascular cutaneous transplant, or "free flap", suitable for hand resurfacing is described in detail. Anatomic and clinical indications are stressed, and the operative steps involved in the preparation and transfer of each flap are outlined.

Amputation Stumps↗

Tarsal and carpal coalition and symphalangism of the Fuhrmann type. Report of a family.

We are reporting on fifteen members of a five-generation family (sixty-three members) who had an autosomal dominant osseous disorder that was characterized by tarsal and carpal coalition, symphalangism, short first metacarpals, and abnormalities of the elbow, including humeroradial fusion. This family is similar to the one reported by Fuhrmann et al.

Adolescent↗

[Pseudohypoparathyroidism. Analysis of a clinical case with late development].

A case of pseudohypoparathyroidism of characteristic phenotype and metabolism is described. The condition was diagnosed at over 50 years of age following the appearance of hypocalcaemia and calcification of basal ganglia which responded quickly to treatment with vitamin D and orally administered calcium. This case gives the opportunity to describe a rare hereditary disease and discuss which mechanisms triggered off the symptomatology: mechanisms which involve PTH, the action of which is still not fully known.

Calcinosis↗