Article
Another adult with Meier-Gorlin syndrome--insights into the natural history.
Clinical dysmorphology - 1 Jul 2003
Shalev Stavit A, Hall Judith G
Abstract excerpt
The Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder, characterized by bilateral microtia, aplasia or hypoplasia of the patellae, and severe intrauterine and post-natal growth retardation. We describe the phenotype and report the medical history of a 25-year-old woman with MGS. Her phenotypic evolution was characterized by severe growth retardation with decelerated growth of the head and...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.