Congenital radioulnar synostosis

Congenital radioulnar synostosis is a rare bone disorder that may be isolated or associated with other disorders and that is characterized by failure of segmentation of the radius and ulna during embryological development, causing limited rotational movements of the forearm, which may lead to difficulties with some activities of daily living.

Azoospermia

Absence of any measurable level of sperm in his semen.


Total: 1

                      


(per page)
PMID (PMCID)
18177653
MALE Adult
Congenital radioulnar synostosis, azoospermia, and pseudodicentric Y chromosome.
Syed AA, Quinton R.
Fertil Steril. 2008;90(2):425-6.
Congenital radioulnar synostosis, azoospermia, and pseudodicentric Y chromosome.