Meschede D, Kliesch S, Horst J, Nieschlag E
Institute of Human Genetics of the University of Münster, Germany.
Clin Dysmorphol. 1998 Jan;7(1):59-60.
The MURCS association is traditionally regarded as a disorder limited to the female sex. It has been hypothesized that men displaying the combination of azoospermia, segmentation abnormalities of the cervicothoracic spine and renal anomalies may have a male analogue of MURCS. Here we describe a patient with non-obstructive azoospermia and Klippel-Feil anomaly type II and suggest that this may represent another case of 'MURCS in the male'.