Article
Feingold syndrome: Clinical review and genetic mapping
24 Sept 2003
Abstract excerpt
Feingold syndrome is characterized by autosomal dominant inheritance of microcephaly and limb malformations, notably hypoplastic thumbs, and clinodactyly of second and fifth fingers. Syndactyly frequently involves the second and third, as well as the fourth and fifth toes. Approximately one in three Feingold syndrome patients have esophageal or duodenal atresia or both. Anal atresia has been reported in a single...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
