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.

Pierre-Robin sequence

Pierre Robin malformation is a sequence of developmental malformations characterized by micrognathia (mandibular hypoplasia), glossoptosis and cleft palate.

Total: 2

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PMID (PMCID)
16681404	MALE	Infant, Newborn
	Pierre Robin sequence with esophageal atresia and congenital radioulnar synostosis.
	Ozkan KU, Coban YK, Uzel M, Ergun M, Oksuz H. Cleft Palate Craniofac J. 2006;43(3):317-20.
	The association of congenital radioulnar synostosis and esophageal atresia with Pierre Robin sequence has not been previously described.
16681404	MALE	Infant, Newborn
	Pierre Robin sequence with esophageal atresia and congenital radioulnar synostosis.
	Ozkan KU, Coban YK, Uzel M, Ergun M, Oksuz H. Cleft Palate Craniofac J. 2006;43(3):317-20.
	Pierre Robin sequence with esophageal atresia and congenital radioulnar synostosis.