February 1972

Arthrogryposis Multiplex Congenita and the Turner Phenotype

Author Affiliations

From the Department of Pediatrics, Wayne State University School of Medicine, and the Children's Hospital of Michigan, Detroit.

Am J Dis Child. 1972;123(2):141-144. doi:10.1001/archpedi.1972.02110080119014

We report a genetically determined syndrome of arthrogryposis multiplex congenita, pterygium formation, and facial features of the Turner phenotype in two boys and two girls, including a pair of siblings.