Stuve-Wiedemann syndrome (SWS) is, at last, beginning to emerge from t
he shadows of campomelic syndrome as a nosologically and, presumably,
causally-distinct entity, first delineated in 1971 on the basis of 2 a
ffected sisters. The fact that these sisters had an affected double fi
rst cousin supports autosomal-recessive inheritance of SWS. (C) 1996 W
iley-Liss, Inc.