Congenital Radioulnar Synostosis, a case report
M Tantray, A Wani, G Kuchey, M Bhat, G Wali, S Sharma
Citation
M Tantray, A Wani, G Kuchey, M Bhat, G Wali, S Sharma. Congenital Radioulnar Synostosis, a case report. The Internet Journal of Orthopedic Surgery. 2008 Volume 15 Number 1.
DOI: 10.5580/1298
Abstract
Introduction
Congenital radioulnar synostosis is a congenital disorder involving radius and ulna, most commonly the proximal ends. The movements between radius and ulna are restricted and the forearm is fixed in varying degrees of pronation.It is mostly bilateral with familial predisposition (autosomal dominant) Wilkie has noted two types: In type 1 medullary canal of radius and ulna are joined with malformed head of radius which is fused with ulna for several centimeters. The radius is longer and its shaft arches anteriorly.In type 2 the radius is fairly normal and but its proximal end is dislocated either anteriorly or posteriorly and is fused with proximal ulna. This type is usually unilateral and is sometimes associated with deformities like supernumerary thumb; absence of thumb, syndactylism .The disorder may be associated with abnormalities of subcutaneous fascial tissues which may be short and abnormally directed. There is no definitive treatment to restore the movements at radioulnar joints; however osteotomy may be performed to bring the forearm into a more functional position especially if the condition is bilateral. Another study has shown the mobilisation operation by separation of synostosis and placement of faciocutaneous graft between the proximal radius and ulna. This is supplemented with proximal radial osteotomy to reduce the dislocated head of radius. These operations may benefit some patients by bringing the forearm into more functional position.
Case Report
A 3 year old female patient presented to us with parents noticing that the child was unable to supinate both the forearms .There were no other symptoms associated with it. The child was born by normal vaginal delivery and was third in birth order. Other siblings were normal.
On clinical examination the child was unable to fully supinate both the forearms and had multiple constriction bands over both the forearms. The child’s left forearm was pronated to a greater degree than the right as shown in fig.1.
On attempted supination child’s arms got adducted as a compensatory mechanism as shown in figure 2.
Figure 2
Range of motion at wrist and elbow were normal. The rest of the clinical examination was normal.
On Radiological evaluation
On radiography there is fusion of proximal end of radius and ulna with posterior dislocation of radial head and normal development of radius bilaterally. There was no associated significant radiological abnormality.
Figure 3
Childs parents were explained about the problem and were informed about the limited success of surgical management. The child was able to grip and hold bowl of food and was able to take meals unaided, there was not much of the functional impairment. Left forearm was pronated to greater degree than right; this was favorable as child could reach the orifices decreasing the degree of his handicap. The parents were counseled properly .The child is under our follow up and osteotomy has been kept optional in case of any functional impairment.