Proximal radio-ulnar synostosis (RUS) may occur congenitally, either as an
isolated condition or as part of a syndrome, or it may occur as a secondary
complication of forearm trauma. We provide a key for the differential diag
nosis of congenital versus traumatic RUS, and for differentiation between t
ypes of congenital RUS. Congenital cases (CRUS) include absence of fracture
, radial head abnormalities, radial shaft bowing, and absence of a sigmoid
notch, whereas post-traumatic RUS results from either radial neck fracture
or evulsion of the biceps brachii, followed by ossification of the resultin
g haematoma or of the interosseous (IO) membrane. Congenital cases include
those which result from incompetent differentiation of the single mesenchym
al mass that gives rise to the radius and ulna (Type I) and those that resu
lt from radial head dislocation in utero, resulting usually from humeral or
ulnar defects (Type II). Type II CRUS can be differentiated by the presenc
e of radial overgrowth, among other factors. Following these guidelines, we
describe and compare the morphology of three congenital cases from North A
merica. Two present bony fusions and one a functional fusion with radial ov
ergrowth. In each case, CRUS significantly limits both supination and prona
tion. Despite differences among the cases, several morphological accommodat
ions are shared as a result of fixation in the neutral (semi-pronated) posi
tion. These changes include the ventral migration of the IO crests of the u
lnae and enlargement of the dorsal tubercles of the radius. Understanding t
he pattern of accommodations made in the face of compromised function ultim
ately increases our understanding of the patterns of growth in normal funct
ional regimes. Copyright (c) 2000 John Wiley & Sons, Ltd.