Two new cases of Cumming syndrome confirming autosomal recessive inheritance

We report on two stillborn sisters with generalized hydrops, campomelia, ce rvical lymphocele, and polycystic dysplasia of kidney, liver, and pancreas. This syndrome conforms to that first described by Cumming et al. [Am. J. M ed. Genet. 25:783-790, 1986]. This observation provides additional support for the notion that this syndrome has an autosomal recessive pattern of inh eritance. Am. J. Med. Genet. 82:340-343, 1999. (C) 1999 Wiley-Liss, Inc.